MifeMiso: Mifepristone and Misoprostol Versus Misoprostol Alone in the Medical Management of Missed Miscarriage

• Sponsor: University of Birmingham (Other)
• Overall Status: Completed
• CT.gov ID: NCT03065660
• Collaborator: Birmingham Women's NHS Foundation Trust (Other), Royal Infirmary of Edinburgh (Other), Royal Victoria Infirmary (Other), City Hospitals Sunderland NHS Foundation Trust (Other), Liverpool Women's NHS Foundation Trust (Other), The Leeds Teaching Hospitals NHS Trust (Other), Barts & The London NHS Trust (Other), Queen's Medical Center (Other), Heart of England NHS Trust (Other), University Hospitals Coventry and Warwickshire NHS Trust (Other), Oxford University Hospitals NHS Trust (Other), St Mary's Hospital, London (Other), University College London Hospitals (Other), University Hospital Southampton NHS Foundation Trust (Other), King's College Hospital NHS Trust (Other), University of Edinburgh (Other), University of Nottingham (Other), Queen Mary University of London (Other), University of Warwick (Other), University of Southampton (Other)
• Enrollment: 711
• Locations: 28
• Arms: 2
• Actual Duration (Months): 27.6
• Patients Per Site: 25.4
• Patients Per Site Per Month: 0.9

Study Details

Study Description

Brief Summary

Miscarriage is the most common complication of pregnancy. As many as 15-25% of pregnancies end in miscarriage, and the number of miscarriages in England is estimated to be approximately 125,000 per year. Miscarriage often brings not only physical pain, bleeding and risks of infection, but also psychological impacts on women and their families. This study will focus on women whose pregnancy sac remains inside the womb (known as a missed miscarriage) and opt for medical management of their miscarriage up to 13+6 weeks of pregnancy. NICE currently recommends that a drug called misoprostol (a vaginal pessary or oral tablet that makes the womb contract) should be used in the medical treatment of miscarriage. However, there is evidence to suggest that combining this drug with mifepristone (an oral tablet that reduces pregnancy hormones) may be more effective in treating miscarriage. Therefore, to test this in a clinical trial, participants will be allocated at random to receive either mifepristone followed by misoprostol, or a dummy drug (placebo) followed by misoprostol. Neither the participants nor the researchers will know what allocation is decided, which is necessary to test the treatments fairly. The main outcome of interest will be whether miscarriage is complete within 7 days of randomisation. If miscarriage is not complete then further treatment (more tablets or surgery) will be offered. A number of other key outcomes, such as the need for an operation, will also be assessed. We will also study the views and experience of the participants regarding the tablet treatment.

We anticipate that 710 women will be required to take part in the study to answer this question with confidence. We estimate that we would be able to recruit this many women in two years.

Condition or Disease	Intervention/Treatment	Phase
Missed Miscarriage	Drug: Mifepristone, Oral, 200 Mg; Drug: Placebo Oral Tablet	Phase 3

Detailed Description

Aim: To investigate the clinical and cost-effectiveness of MifeMiso combination (mifepristone and misoprostol) versus misoprostol alone in the management of missed miscarriage.

Primary clinical objective: To test the hypothesis that treatment with mifepristone plus misoprostol is superior to misoprostol alone for the resolution of miscarriage within 7 days in women diagnosed with missed miscarriage by pelvic ultrasound scan in the first 13+6 weeks of pregnancy.

Key secondary objective:To test the hypothesis that the addition of mifepristone reduces the need for surgical intervention to resolve the miscarriage.

Other secondary objectives:

1. To evaluate if the addition of mifepristone reduces the need for further doses of misoprostol.

2. To evaluate if the addition of mifepristone improves other clinical outcomes including surgical intervention up to and including 7 days post-randomisation and after 7 days post-randomisation, duration of bleeding, infection, negative pregnancy test at 21 days post-randomisation, time from randomisation to discharge from EPU care, side effects and complications.

3. To evaluate if the addition of mifepristone improves patient satisfaction

4. To assess the cost-effectiveness of the combination of mifepristone and misoprostol in the medical management of missed miscarriage.

Economic objectives: To assess the cost-effectiveness of the combination of mifepristone and misoprostol in the medical management of missed miscarriage based on an outcome of additional cost per additional successfully managed miscarriage and additional cost per additional quality-adjusted life-year (QALY). Using a model-based economic evaluation we will further explore the cost-effectiveness of the medical management of missed miscarriage, as explored in the proposed trial, with alternative management strategies, such as surgical and expectant, based on available secondary sources.

Mixed-method evaluation objectives: To explore the satisfaction of patients who complete the trial protocol. The results of the satisfaction survey (CSQ-8) will act as a sampling frame to conduct semi-structured interviews to further investigate patient experiences and satisfaction with medical management of missed miscarriage.

Study Design

• Study Type: Interventional
• Actual Enrollment: 711 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Intervention Model Description: A randomised, parallel group, double-blind, placebo-controlled multicentre study, with health economic and mixed-methods evaluation.A randomised, parallel group, double-blind, placebo-controlled multicentre study, with health economic and mixed-methods evaluation.
• Masking: Triple (Participant, Care Provider, Investigator)
• Masking Description: Participants, investigators, research midwives/nurses and other attending clinicians will remain blind to the trial drug allocation throughout the duration of the trial.
• Primary Purpose: Treatment
• Official Title: A Randomised Placebo-controlled Trial of Mifepristone and Misoprostol Versus Misoprostol Alone in the Medical Management of Missed Miscarriage
• Actual Study Start Date: Sep 20, 2017
• Actual Primary Completion Date: Jan 9, 2020
• Actual Study Completion Date: Jan 9, 2020

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Mifepristone A single dose of oral mifepristone 200mg, followed by a single dose of vaginal, oral or sublingual misoprostol 800mcg 2 days later	Drug: Mifepristone, Oral, 200 Mg; The Investigational Medicinal Product (IMP) is a single dose of 200mg mifepristone to be taken orally after confirmation of missed miscarriage by pelvic ultrasound scan.; Other Names: Mifegyne
Placebo Comparator: Placebo Oral placebo tablet followed by a single dose of vaginal, oral or sublingual misoprostol 800mcg 2 days later.	Drug: Placebo Oral Tablet; The placebo will be an oral tablet in the same form as the IMP, and identical in appearance.

Outcome Measures

Primary Outcome Measures

1. Failure to spontaneously pass the gestational sac within 7 days after randomisation [Within 7 days after randomisation]

   To test the hypothesis that treatment with mifepristone plus misoprostol is superior to misoprostol alone for the resolution of miscarriage within 7 days in women diagnosed with missed miscarriage by pelvic ultrasound scan in the first 13+6 weeks of pregnancy.

Secondary Outcome Measures

1. Surgical intervention to resolve the miscarriage (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Surgical intervention to resolve the miscarriage

2. Surgical intervention to resolve the miscarriage up to and including day 7 post-randomisation [From randomisation until day 7 post-randomisation]

   Surgical intervention to resolve the miscarriage

3. Surgical intervention to resolve the miscarriage after day 7 post-randomisation to discharge from EPU care [From day 8 post-randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Surgical intervention to resolve the miscarriage

4. Need for further doses of misoprostol up to day 7 post-randomisation [After initial 800mcg dose of misoprostol at day 2 until day 7 post-randomisation]

   Need for further doses of misoprostol up to day 7 post-randomisation

5. Need for further doses of misoprostol up to discharge from EPU care [After initial 800mcg dose of misoprostol at day 2 until discharge from EPU care; assessed up to approximately 8 weeks]

   Need for further doses of misoprostol up to discharge from EPU care

6. Overall patient satisfaction score (measured using the CSQ-8 questionnaire and collected upon discharge from EPU care). [Within 6 weeks of discharge from EPU care]

   Overall patient satisfaction score (measured using the CSQ-8 questionnaire and collected upon discharge from EPU care).

7. Patient quality of life (Index value and overall health status measured using the EQ-5D-5L questionnaire [Completion on date of randomisation, day 6-7 post-randomisation or day of follow-up USS if different to day 6-7 and day 21 +/- 2 days post-randomisation. Completion of all patient quality of life assessments up to approximately 8 weeks post-randomisation]

   Patient quality of life (Index value and overall health status measured using the EQ-5D-5L questionnaire and collected on date of randomisation, day 6-7 post-randomisation or day of follow-up USS if different to day 6-7 and day 21 +/- 2 days post-randomisation. If a woman obtains an initial positive pregnancy test result at day 21 +/- 2 days post-randomisation then a further EQ-5D-5L questionnaire is collected upon discharge from EPU care).

8. Duration of bleeding reported by woman (days). (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Duration of bleeding reported by woman (days). (collected up to discharge from EPU care)

9. Diagnosis of infection associated with miscarriage requiring outpatient antibiotic treatment (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Diagnosis of infection associated with miscarriage requiring outpatient antibiotic treatment (collected up to discharge from EPU care)

10. Diagnosis of infection associated with miscarriage requiring inpatient antibiotic treatment (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

    Diagnosis of infection associated with miscarriage requiring inpatient antibiotic treatment (collected up to discharge from EPU care)

11. Negative pregnancy test result 21 days (± 2 days) after randomisation. [21 days (± 2 days) after randomisation.]

    Negative pregnancy test result 21 days (± 2 days) after randomisation.

12. Time from randomisation to discharge from EPU care (described using summary statistics only) [Time from randomisation to discharge from EPU care; assessed up to approximately 8 weeks]

    Time from randomisation to discharge from EPU care.

13. Blood transfusion required (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

    Blood transfusion required (collected up to discharge from EPU care)

14. Side effects (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

    Side effects (collected up to discharge from EPU care)

15. Death (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

    Death (collected up to discharge from EPU care)

16. Any serious complications (collected up to discharge from EPU care) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

    Any serious complications (collected up to discharge from EPU care)

Other Outcome Measures

1. Outpatient or emergency visits [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Number of outpatient or emergency visits

2. Inpatient admissions (nights in hospital) [From randomisation until discharge from EPU care; assessed up to approximately 8 weeks]

   Number of inpatient admissions (nights in hospital)

Eligibility Criteria

Criteria

• Ages Eligible for Study: 16 Years and Older
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Women diagnosed with missed miscarriage by pelvic ultrasound scan in the first 13+6 weeks of pregnancy that choose to have medical management of miscarriage.

• Age 16 years and over

• Willing and able to give informed consent.

Exclusion Criteria:

• Women opting for alternative methods of miscarriage management (expectant or surgical)

• Diagnosis of incomplete miscarriage.

• Life threatening bleeding.

• Contraindications to mifepristone or misoprostol use for example chronic adrenal failure, known hypersensitivity to either drug, haemorrhagic disorders and anticoagulant therapy, prosthetic heart valve or history of endocarditis, existing cardiovascular disease, severe asthma uncontrolled by therapy or inherited porphyria.

• Participation in any other blinded, placebo-controlled trials of investigational medicinal products in pregnancy.

• Previous participation in the MifeMiso trial

• Woman not able to attend for day 6-7 ultrasound scan

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Birmingham Heartlands Hospital	Birmingham		United Kingdom
2	Birmingham Women's Hospital	Birmingham		United Kingdom
3	Southmead Hospital	Bristol		United Kingdom
4	St Michael's Hospital	Bristol		United Kingdom
5	Burnley General Hospital	Burnley		United Kingdom
6	University Hospital Coventry	Coventry		United Kingdom
7	Royal Infirmary of Edinburgh	Edinburgh		United Kingdom
8	Epsom Hospital	Epsom		United Kingdom
9	St Helier Hospital	Epsom		United Kingdom
10	Glasgow Royal Infirmary	Glasgow		United Kingdom
11	Queen Elizabeth University Hospital	Glasgow		United Kingdom
12	Liverpool Women's Hospital	Liverpool		United Kingdom
13	Chelsea and Westminster Hospital	London		United Kingdom
14	Kings College Hospital	London		United Kingdom
15	Newham University Hospital	London		United Kingdom
16	Royal London Hospital	London		United Kingdom
17	St Thomas' Hospital	London		United Kingdom
18	University College Hospital London	London		United Kingdom
19	West Middlesex Hospital	London		United Kingdom
20	Whipps Cross University Hospital	London		United Kingdom
21	Royal Victoria Infirmary	Newcastle		United Kingdom
22	Queen's Medical Centre	Nottingham		United Kingdom
23	Queen Alexandra Hospital	Portsmouth		United Kingdom
24	Princess Anne Hospital	Southampton		United Kingdom
25	Sunderland Royal Hospital	Sunderland		United Kingdom
26	Princess of Wales Hospital	Swansea		United Kingdom
27	Singleton Hospital	Swansea		United Kingdom
28	Princess Royal Hospital	Telford		United Kingdom

Sponsors and Collaborators

• University of Birmingham
• Birmingham Women's NHS Foundation Trust
• Royal Infirmary of Edinburgh
• Royal Victoria Infirmary
• City Hospitals Sunderland NHS Foundation Trust
• Liverpool Women's NHS Foundation Trust
• The Leeds Teaching Hospitals NHS Trust
• Barts & The London NHS Trust
• Queen's Medical Center
• Heart of England NHS Trust
• University Hospitals Coventry and Warwickshire NHS Trust
• Oxford University Hospitals NHS Trust
• St Mary's Hospital, London
• University College London Hospitals
• University Hospital Southampton NHS Foundation Trust
• King's College Hospital NHS Trust
• University of Edinburgh
• University of Nottingham
• Queen Mary University of London
• University of Warwick
• University of Southampton

Investigators

• Principal Investigator: Arri Coomarasamy, University of Birmingham

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• Trial website

Publications

None provided.

• Responsible Party: University of Birmingham
• ClinicalTrials.gov Identifier: NCT03065660
• Other Study ID Numbers: RG_16-076; 15/160/02; 2016-005097-35
• First Posted: Feb 28, 2017
• Last Update Posted: Apr 9, 2020
• Last Verified: Apr 1, 2020

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Product Manufactured in and Exported from the U.S.: No
• Keywords provided by University of Birmingham: Missed miscarriage; Mifepristone; Misoprostol; Medical management
• Additional relevant MeSH terms: Abortion, Spontaneous; Abortion, Missed; Mifepristone

Study Results

No Results Posted as of Apr 9, 2020