Trials / Completed
CompletedNCT03202836
Vaginal Progesterone Supplementation in the Management of Preterm Labor
Vaginal Progesterone Supplementation in the Management of Preterm Labor: A Randomized, Double Blind, Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Chulalongkorn University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
This study evaluates the addition of vaginal progesterone in the management of preterm labor. Half of participants will receive vaginal progesterone, tocolysis and corticosteroid, while the other half will receive only tocolysis and corticosteroid.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | progesterone | vaginal utrogestan |
| DRUG | Tocolytics | tocolysis for 48 hours |
| DRUG | Steroids | antenatal corticosteroids for 48 hours |
Timeline
- Start date
- 2017-06-29
- Primary completion
- 2018-07-30
- Completion
- 2018-07-31
- First posted
- 2017-06-29
- Last updated
- 2019-01-31
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT03202836. Inclusion in this directory is not an endorsement.