Clinical Trials Directory

Trials / Completed

CompletedNCT03023514

Lipoic Acid Supplementation in IVF

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
172 (actual)
Sponsor
Lo.Li.Pharma s.r.l · Industry
Sex
Female
Age
30 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Alpha-Lipoic Acid (ALA) is a natural molecule that can make a significant contribution to the success of embryo implantation phase, because it exerts, directly or indirectly, an immunomodulatory activity. ALA has the ability to regenerate antioxidants molecules that facilitate embryo implantation, and to stimulate the production of local mediators useful for implantation. This study is a prospective clinical trial and aims to evaluate the reproductive outcomes of Italian couples following oocyte donation fresh cycles when receiving per os tablets of lipoic acid. Indeed, the control group had only the standard treatment (vaginal progesterone), whereas the study group, in addition to that, received ALA (300 mg, 2 times per day) by oral route, from the day of donors oocyte pick up until the pregnancy test. If the childbearing occurred, treatment continued until the 8th week of pregnancy. Primary outcome of the study is the implantation rate while the positive hCG rate, the clinical pregnancy rate, the miscarriage rate and the live-birth rate are secondary outcomes .

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOral Lipoic acid300 mg ALA x2 (1pill orally/12h) to the recipient from the day of the donors pick up until 8 week of pregnancy
DRUGVaginal Progesterone200 mg Vaginal Progesterone (1 vaginal capsule/24h) from the day of the donors pick up until 8 week of pregnancy

Timeline

Start date
2015-03-01
Primary completion
2016-06-01
First posted
2017-01-18
Last updated
2017-01-19

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT03023514. Inclusion in this directory is not an endorsement.

Lipoic Acid Supplementation in IVF (NCT03023514) · Clinical Trials Directory