Calcium Channel Blockers Compared to Magnesium Sulfate in Fetal Cerebral Blood Flow

Sponsor
Kasr El Aini Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02591004
Collaborator
(none)
130
1
2
23
5.6

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the possible use of calcium channel as a neuroprotectant in cases with PTL. This will be done by comparing the effect they have on cerebral blood vessels with the already established MgSo4. They have been proven superior to magnesium sulphate in tocolysis, and they possess the mechanism of action that would allow for their theoretical use as neuroprotective agents.

Condition or Disease Intervention/Treatment Phase
  • Drug: Magesium sulphate
  • Drug: Nifedipine
  • Radiation: Doppler on fetal middle cerebral artery
Phase 2/Phase 3

Detailed Description

After internal review board approval from the obstetrics and gynecology department of Kasr Alainy hospital, 130 patients will be recruited in a randomized case control study. The patients will be recruited from the emergency admissions department, after fulfilling the recruitment criteria. In an independent case-control study the Sample size was calculated using an odds ratio of exposure to CP of 0.14 (95% CI 0.05-0.51) (Grether et.al, 1998), where the alpha level error was fixed at 0.5 and the power was set at 80%, the optimal sample size was calculated to be 65 patients in each arm.

Patients will be randomized on admission by nurse in labor ward into either one of two groups. Group A will receive MgSo4, while group B will receive Nifedipine ( Epilat 20mg ® EIPICO Egypt ). Randomization will be achieved through a computer generated randomization table. Recruitment will continue till 65 patients will be allocated to each group.

Patients in group A will receive 4 gm intravenous (I.V) MgSo4 loading dose over 30 mins & 1 gm/ hour maintenance dose for 24 hours, or till labor occurs ( whichever occurs first) , this does is given in accordance with Australian Research Centre for Health of Women and Babies, 2010, for using MgSo4 for neuroprotection against CP.

While patients in group B will receive Nifedipine ( Epilat 10mg ® EIPICO Egypt ), as there is no recommended dose for the use of nifedipine as neuroprotectant, the dose given in this study will be same as that used for tocolysis. Nifedipine wil be given in a loading dose of 40 mg in the 1st hour (10mg will be given every 15 min), then a maintenance dose of 60mg /24 hours, divided in 3 doses (Hösli et.al, 2014).

The ability of the MgSo4 as a neuro protectant is dependent on its cerebral vasodilating effects (Magee et.al,2011; Macdonald et.al, 2004), therefore we propose to measure the mean pulsility index (PI) and resistance index (PI) of the middle cerebral artery in the fetus twice, once before giving them the drug, and the other after 4 hours of starting the loading dose. All ultrasound and power doppler examinations will be carried out by the same investigator, using the Voluson 730 machine (GE Healthcare Austria GmbH, Seoul, Korea). Sample size calculation was done using Stats Direct statistical software version 2.7.2 for MS Windows, StatsDirect Ltd., Cheshire, UK.

Study Design

Study Type:
Interventional
Actual Enrollment :
130 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Comparing Fetal Cerebral Blood Flow Between Magnesium Sulfate & Calcium Channel Blockers in Patients With Preterm Labor; a Randomized Controlled Trial.
Study Start Date :
Dec 1, 2015
Actual Primary Completion Date :
Oct 1, 2017
Actual Study Completion Date :
Nov 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Magesium sulphate

Patients in group A will receive Magesium sulphate 4 gm intravenous (I.V) loading dose over 30 mins & 1 gm/ hour maintenance dose for 24 hours, or till labor occurs ( whichever occurs first). Doppler on fetal middle cerebral artery

Drug: Magesium sulphate
*Experimental: Group A: Magesium sulphate 4 gm intravenous (I.V) loading dose over 30 mins & 1 gm/ hour maintenance dose for 24 hours, or till labor occurs ( whichever occurs first)
Other Names:
  • MgSo4
  • Radiation: Doppler on fetal middle cerebral artery
    both group A and group B: ultrasound doppler to measure the mean pulsility index (PI) and resistance index (PI) of the middle cerebral artery in the fetus twice, once before giving them the drug, and the other after 4 hours of starting the loading dose.

    Active Comparator: Nifedipine

    Patients in group B will receive Nifedipine ( Epilat 10mg ® EIPICO Egypt ), as there is no recommended dose for the use of nifedipine as neuroprotectant, the dose given in this study will be same as that used for tocolysis. Nifedipine wil be given in a loading dose of 40 mg in the 1st hour (10mg will be given every 15 min), then a maintenance dose of 60mg /24 hours, divided in 3 doses. Doppler on fetal middle cerebral artery

    Drug: Nifedipine
    *Active Comparator: Group B Nifedipine wil be given in a loading dose of 40 mg in the 1st hour (10mg will be given every 15 min), then a maintenance dose of 60mg /24 hours, divided in 3 doses
    Other Names:
  • Epilat
  • Radiation: Doppler on fetal middle cerebral artery
    both group A and group B: ultrasound doppler to measure the mean pulsility index (PI) and resistance index (PI) of the middle cerebral artery in the fetus twice, once before giving them the drug, and the other after 4 hours of starting the loading dose.

    Outcome Measures

    Primary Outcome Measures

    1. difference in mean doppler indicies of middle cerebral artery of fetus between both groups [4 hours]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 35 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    • Inclusion Criteria:

    • in imminent preterm labour ( , >4cm dilated, cervical effacement > 60%).

    • < 32 weeks gestational age.

    • Exclusion Criteria:

    • patients will be excluded from the study if the gestational age was > 32 weeks

    • intrauterine fetal death

    • multiple gestation

    • fetal malformations where only palliative care is needed

    • placental abruption

    • Chorioamnionitis

    • pre-ecplamsia, or diabetes

    • suspected fetal compromise diagnosed by ultrasound or CTG requiring delivery, -any indication for caesarean section

    • fetal growth restriction

    • Also any contraindication to the use of Nifedipine e.g maternal cardiac disease, allergy to Nifedipine, hypotension, or hepatic dysfunction

    • Contraindications To MgSo4 use as Myasthenia Gravis, progressive muscle weakness ,allergy to MgSo4, severe renal impairment & heart block.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 11562 Cairo Egypt 11562

    Sponsors and Collaborators

    • Kasr El Aini Hospital

    Investigators

    • Principal Investigator: Ahmed M Kamel, M.D., Lecturer of obstetrics & Gynecology
    • Principal Investigator: Wafaa Eldesouky, M.D., Lecturer of obstetrics & Gynecology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Ahmed M.Kamel, Lecturer of obstetrics & Gynecology, Kasr El Aini Hospital
    ClinicalTrials.gov Identifier:
    NCT02591004
    Other Study ID Numbers:
    • A21102015
    First Posted:
    Oct 29, 2015
    Last Update Posted:
    Nov 17, 2017
    Last Verified:
    Nov 1, 2017
    Keywords provided by Ahmed M.Kamel, Lecturer of obstetrics & Gynecology, Kasr El Aini Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 17, 2017