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Magnesium sulfate and nifedipine on treatment of preterm labor

Comparison the effect of magnesium sulfate and nifedipine in the successful treatment of preterm labor

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012062310089N1
Enrollment
100
Registered
2013-06-07
Start date
2003-03-03
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm labor and delivery. Preterm spontaneous labor with term delivery

Interventions

Intervention 1: Intravenous loading dose infusion was 4gr magnesium sulfate (20%) during 30 minutes, followed by a maintenance dose of 2 gr/hr until stopping or reducing uterine contractions. (magnes
until a maximum dose of 40mg for one hour. Depending on tocolytic effects of nifedipine that we have used during one hour, we used a minimal dose of 60 mg every day. After 3 days, the dose would be de
Treatment - Drugs
Intravenous loading dose infusion was 4gr magnesium sulfate (20%) during 30 minutes, followed by a maintenance dose of 2 gr/hr until stopping or reducing uterine contractions. (magnesium sulfate hep
We have used one capsule nifedipine (10 mg sublingual from Dana pharmaceutical company, Iran and its Generic name was Nifi-Gel). If uterine contractions persisted, we would use another capsule every 1

Sponsors

Vice Chancellor for Research, Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Singleton pregnancy, 24 to 37 weeks of gestation, signs of preterm labor. Exclusion criteria : premature rupture of membrane, cervical dilatation > 4 cm, gestational age 37 weeks, chorioamnionitis, vaginal bleeding, multiple pregnancy, previous cesarean section, previous uterus surgery, maternal or fetal indications for termination of pregnancy such as preeclampsia, fetal distress, fetal growth abnormalities and decreased blood pressure.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Delaying delivery up to 48 hours. Timepoint: Every 15 minutes until stopping of uterine contractions. Method of measurement: Abdominal palpation of uterus.

Secondary

MeasureTime frame
Cervical dilatation. Timepoint: Every 2 hours until stopping of uterine contractions. Method of measurement: Vaginal examination.;Uterine contractions. Timepoint: Every 15 minutes until stopping of uterine contractions. Method of measurement: Abdominal palpation of uterus.;Cervical effacement. Timepoint: Every 2 hours until stopping of uterine contractions. Method of measurement: Vaginal examination.;Fetal complications. Timepoint: During drug administration. Method of measurement: Physician assessment.;Maternal complications. Timepoint: During drug administration. Method of measurement: Physician assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Roya Faraji Darkhaneh

Guilan University of Medical Sciences

royafaraji1371@yahoo.com+98 13 1322 5624

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026