Trials / Completed
CompletedNCT02601898
Vaginal Administration of ALA vs Progesterone for the Subchorionic Hematoma Treatment
Vaginal Administration of Alpha Lipoic Acid vs Progesterone for the Subchorionic Hematoma Treatment
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 54 (actual)
- Sponsor
- Azienda USL Ferrara · Other Government
- Sex
- Female
- Age
- 24 Years – 37 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study was to compare the therapeutic efficacy of lipoic acid versus progesterone by vaginal administration on subchorionic hematoma resorption in women at the first trimester of pregnancy with threatened miscarriage.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lipoic acid | Vaginal capsules (medical device) containing 10 mg of lipoic acid (1 per day) |
| DRUG | Progesterone | Vaginal capsules (drug) containing 200 mg of progesterone (2 per day) |
Timeline
- Start date
- 2015-01-01
- Primary completion
- 2015-11-01
- First posted
- 2015-11-11
- Last updated
- 2016-01-08
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT02601898. Inclusion in this directory is not an endorsement.