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

Primary Purpose

Preterm Labor, Cerebral Palsy

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Magesium sulphate
Nifedipine
Doppler on fetal middle cerebral artery
Sponsored by
Kasr El Aini Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preterm Labor focused on measuring Neuroprotection, calcium channel blockers, magnesium sulhate, Middle cerebral artery doppler

Eligibility Criteria

20 Years - 35 Years (Adult)FemaleAccepts Healthy Volunteers
  • 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.

Sites / Locations

  • 11562

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Magesium sulphate

Nifedipine

Arm Description

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

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

Outcomes

Primary Outcome Measures

difference in mean doppler indicies of middle cerebral artery of fetus between both groups

Secondary Outcome Measures

Full Information

First Posted
October 26, 2015
Last Updated
November 15, 2017
Sponsor
Kasr El Aini Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02591004
Brief Title
Calcium Channel Blockers Compared to Magnesium Sulfate in Fetal Cerebral Blood Flow
Official Title
Comparing Fetal Cerebral Blood Flow Between Magnesium Sulfate & Calcium Channel Blockers in Patients With Preterm Labor; a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
December 2015 (undefined)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
November 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kasr El Aini Hospital

4. Oversight

Data Monitoring Committee
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Labor, Cerebral Palsy
Keywords
Neuroprotection, calcium channel blockers, magnesium sulhate, Middle cerebral artery doppler

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Magesium sulphate
Arm Type
Experimental
Arm Description
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
Arm Title
Nifedipine
Arm Type
Active Comparator
Arm Description
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
Intervention Type
Drug
Intervention Name(s)
Magesium sulphate
Other Intervention Name(s)
MgSo4
Intervention Description
*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)
Intervention Type
Drug
Intervention Name(s)
Nifedipine
Other Intervention Name(s)
Epilat
Intervention Description
*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
Intervention Type
Radiation
Intervention Name(s)
Doppler on fetal middle cerebral artery
Intervention Description
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.
Primary Outcome Measure Information:
Title
difference in mean doppler indicies of middle cerebral artery of fetus between both groups
Time Frame
4 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed M Kamel, M.D.
Organizational Affiliation
Lecturer of obstetrics & Gynecology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wafaa Eldesouky, M.D.
Organizational Affiliation
Lecturer of obstetrics & Gynecology
Official's Role
Principal Investigator
Facility Information:
Facility Name
11562
City
Cairo
ZIP/Postal Code
11562
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
21639972
Citation
Magee L, Sawchuck D, Synnes A, von Dadelszen P; MAGNESIUM SULPHATE FOR FETAL NEUROPROTECTION CONSENSUS COMMITTEE; MATERNAL FETAL MEDICINE COMMITTEE. SOGC Clinical Practice Guideline. Magnesium sulphate for fetal neuroprotection. J Obstet Gynaecol Can. 2011 May;33(5):516-529. doi: 10.1016/S1701-2163(16)34886-1.
Results Reference
background
PubMed Identifier
24385286
Citation
Hosli I, Sperschneider C, Drack G, Zimmermann R, Surbek D, Irion O; Swiss Society of Obstetrics and Gynecology. Tocolysis for preterm labor: expert opinion. Arch Gynecol Obstet. 2014 Apr;289(4):903-9. doi: 10.1007/s00404-013-3137-9. Epub 2014 Jan 3.
Results Reference
background
Citation
Australian Research Centre for Health of Women and Babies. Antenatal Magnesium Sulphate Prior to Preterm Birth for Neuroprotection of the Fetus, Infant and Child - National Clinical Practice Guidelines. Adelaide. ARCH; 2010 [www.adelaide.edu.au/arch/].
Results Reference
background
PubMed Identifier
14743919
Citation
Macdonald RL, Curry DJ, Aihara Y, Zhang ZD, Jahromi BS, Yassari R. Magnesium and experimental vasospasm. J Neurosurg. 2004 Jan;100(1):106-10. doi: 10.3171/jns.2004.100.1.0106.
Results Reference
background
PubMed Identifier
9457123
Citation
Grether J, Hirtz D, McNellis D, Nelson K, Rouse DJ. Tocolytic magnesium sulphate and paediatric mortality. Lancet. 1998 Jan 24;351(9098):292; author reply 293. doi: 10.1016/S0140-6736(05)78239-8. No abstract available.
Results Reference
background

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

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