Clinical Trials Directory

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

TypeNameDescription
DEVICELipoic acidVaginal capsules (medical device) containing 10 mg of lipoic acid (1 per day)
DRUGProgesteroneVaginal 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.