Overview

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