Hysteroscopy Before in Vitro Fertilization - Does it Improve the Outcome?

Sponsor
Hvidovre University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01743391
Collaborator
Holbaek Sygehus (Other)
220
1
2
65
3.4

Study Details

Study Description

Brief Summary

By randomizing sub-fertile women to either control or office-hysteroscopy in the circle prior to IVF or ICSI (intracytoplasmatic sperm injection

) treatment, we aim to enlighten whether hysteroscopy with endometrial biopsy increases pregnancy rates in the intervention group.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Office-hysteroscopy with biopsy
N/A

Detailed Description

Background A tenth of a population in Denmark today is the result of assisted fertility, including IVF and ICSI. In roughly 40 % of these subfertile women the reason is unknown. Standard initial procedures include transvaginal ultrasonography, with or without saline infusion to detect intrauterine abnormalities that might explain the infertile condition. The golden standard to detect intrauterine abnormalities is hysteroscopy. Such abnormalities can be detected in a fourth of this population. Earlier studies indicate that the hysteroscopy alone - without correcting any abnormalities, affects IVF/ISCI outcome positively.

Aim By randomizing patients referred to the fertility clinic to ±office-hysteroscopy in circle prior to IVF/ISCI, we aim to enlighten whether mini-hysteroscopy with endometrial biopsy will increase the fertility by looking at pregnancy rates as our main outcome.

Method Women signed up for second IVF/ISCI treatment will be recruited, after signed consent they are randomized to either office-hysteroscopy or nothing before standard treatment in the fertility clinic.

Mini-hysteroscopy is a standard procedure in our gynecological outpatient clinic. The procedure is done without any anesthetics. Only women with normal intrauterine conditions will be enrolled in this protocol.

When the fertility clinic has a positive serum-HCG (human chorionic gonadotropin

) and a positive transvaginal sonography, pregnancy is confirmed. If negative serum-HCG, negative pregnancy will be registered.

Study Design

Study Type:
Interventional
Actual Enrollment :
220 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Hysteroscopy Before in Vitro Fertilization - Does it Improve the Outcome?
Study Start Date :
Jan 1, 2013
Actual Primary Completion Date :
Jan 1, 2018
Actual Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control

Standard treatment

Experimental: Intervention

Office-hysteroscopy with endometrial biopsy before standard treatment

Procedure: Office-hysteroscopy with biopsy

Outcome Measures

Primary Outcome Measures

  1. pregnancy rates [individual outcome will be evaluated within 8 weeks after IVF treatment. Over all outcome will be evaluated after 3 years.]

    Positive serum HCG and transvaginal ultrasonography, alternatively negative serum HCG and negative outcome will be registrated. After 300 women have been included final outcome will be evaluated.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Women submitted to IVF or ISCI treatment

  • Age > 18 years

  • Women able to read, speak and understand Danish

  • Written consent

Exclusion Criteria:
  • Intrauterine abnormalities

  • Infection

  • BMI > 35

  • Known intrauterine cause to the infertile condition

  • Abuse of alcohol or drugs

  • Untreated medical condition

  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hvidovre Hospital, Department of Gynecology and Obstetrics Copenhagen Hvidovre Denmark 2650

Sponsors and Collaborators

  • Hvidovre University Hospital
  • Holbaek Sygehus

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kristine Juul Hare, PhD, MD, Hvidovre University Hospital
ClinicalTrials.gov Identifier:
NCT01743391
Other Study ID Numbers:
  • H-4-2012-158
First Posted:
Dec 6, 2012
Last Update Posted:
Mar 29, 2022
Last Verified:
Mar 1, 2022
Keywords provided by Kristine Juul Hare, PhD, MD, Hvidovre University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 29, 2022