Comparison the effect of Progestrone and Nifedipine in prevention of preterm delivery

Phase 2

• Conditions: Preterm delivery.; Preterm labour and delivery

• Registration Number: IRCT2017031133016N1
• Lead Sponsor: Vice chancellor for research, Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

Main exclusion criteria: diabetes; hypertension; seizure; migraine; heart disease; kidney disease; asthma; active liver disease; thrombophlebitis; cervix insufficiency; twins and more pregnancy; cervical dilation = 4 cm; intrauterine growth retardation; PROM; vaginal bleeding; tocolysis contraindications include fetal distress, chorioamnionitis, severe preeclampsia, hemodynamic instability; trauma history; smoking; history of taking cimetidine, beta blockers, digoxin or nitrates

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of uterine contractions. Timepoint: Every 20 minutes after the treatment start. Method of measurement: Manual by.