Efficacy of Oral Progesterone and Vaginal Progesterone After Tocolytic Therapy in Threatened Preterm Labor

• Status: Completed
• Trial end date: 2017-03-01
• Target enrollment: 0
• Participant gender: Female

Summary

The purpose of this study is to determine efficacy of vaginal and oral progesterone after tocolytic therapy in threatened preterm labor

• Phase: Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Sanpasitthiprasong Hospital
• Treatments: Dydrogesterone; Progesterone; Tocolytic Agents

Criteria

Inclusion Criteria:

• Single pregnancies of 28 to 33 weeks and 6 days who had been experienced for threatened or preterm labor with intact membrane

Exclusion Criteria:

• Proven membranes ruptured

• Ultrasonographically found placenta previa, multiple pregnancy, fetal anomaly

• Aneuploidy detected.

• Had emergency condition that required for emergency delivery such as fetal distress, chorioamnionitis, prolapsed cord