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Indomethacin Versus Nifedipine for Preterm Labor Tocolysis

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Stanford University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Obstetric Labor, Premature

Treatments

Drug: Indomethacin
Drug: Nifedipine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Indomethacin and Nifedipine are commonly used medications for treatment of pre term labor. This study will compare the efficacy and adverse outcomes of oral nifedipine versus oral indomethacin for preterm labor tocolysis in an effort to identify which drug is most effective.

Patients diagnosed with preterm labor who grant consent will be randomized by the pharmacy to receive oral nifedipine or oral indomethacin. Both the patient and primary medical provider will be blinded to the identity of the study drug. An abdominal ultrasound will be performed in the labor and delivery unit prior to the administration of the tocolytic in order to assess fetal position and fluid level, and to document fetal cardiac activity and movement, and will be repeated at 48 hours post-randomization. Following randomization, the patient will be given either 50 mg oral indomethacin with two pills of placebo, or 3 pills each containing 10 mg oral nifedipine for a total of 30 mg. The patients will then receive either 25 mg of oral indomethacin every 6 hours for 48 hours, or 20 mg of oral nifedipine every 6 hours for 48 hours. Tocolysis beyond 48 hours will not be used.

Full description

Patients presenting between 24-34 weeks gestation diagnosed with preterm labor who grant consent will be randomized by the pharmacy to receive oral nifedipine or oral indomethacin. Both the patient and primary medical provider will be blinded to the identity of the study drug. An abdominal ultrasound will be performed in the labor and delivery unit prior to the administration of the tocolytic in order to assess fetal position and fluid level, and to document fetal cardiac activity and movement, and will be repeated at 48 hours post-randomization. Following randomization, the patient will be given either 50 mg oral indomethacin with two pills of placebo, or 3 pills each containing 10 mg oral nifedipine for a total of 30 mg. The patients will then receive either 25 mg of oral indomethacin every 6 hours for 48 hours, or 20 mg of oral nifedipine every 6 hours for 48 hours. Tocolysis beyond 48 hours will not be used. Antibiotics and steroids for fetal lung maturity will be administered as per standard of care for preterm labor. Maternal side effects and delivery outcomes will be assessed from questionnaires administered by the study team following treatment, and/or from review of the patient's medical records.

Enrollment

29 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Singleton and twin gestations
  • Intact amniotic membranes
  • No contra-indications to tocolysis
  • 24-34 weeks gestation by last menstrual period and/or ultrasound
  • Documented cervical change, and regular painful uterine contractions at least every 5 minutes, or at least 2 cm cervical dilation and 80% effacement

Exclusion criteria

  • Ruptured amniotic membranes
  • Signs/symptoms of chorioamnionitis (maternal temperature greater than 100.4 F/38.0 C, fetal tachycardia, uterine tenderness)
  • Non-reassuring fetal heart rate tracings
  • Contra-indications to indomethacin or nifedipine
  • Contra-indications to tocolysis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

29 participants in 2 patient groups

Indomethacin
Active Comparator group
Description:
50 mg. oral Indomethacin initially, followed by 25 mg every 6 hrs for 48 hrs.
Treatment:
Drug: Indomethacin
Nifedipine
Active Comparator group
Description:
30 mg Nifedipine initially followed by 20 mg every 6 hrs for 48 hrs.
Treatment:
Drug: Nifedipine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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