Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06426355

The Effeciency of NMN in Improving IVF/ICSI-ET Pregnancy Outcomes in Patients With DOR

The Effeciency of Nicotinamide Mononucleotide (NMN) in Improving IVF/ICSI-ET Pregnancy Outcomes in Patients With Decreased Ovarian Reserve(DOR): a Randomized Double-blind Placebo Control Clinical Trail

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to understand the effect of nicotinamide mononucleotide (NMN) on patients with diminished ovarian reserve and the outcomes of IVF/ICSI-ET.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTNMNNMN capsules (total of 600mg/day) for 2-5 months
OTHERPlaceboNMN-free placebo capsules for 2-5 months

Timeline

Start date
2023-10-01
Primary completion
2026-02-01
Completion
2027-02-01
First posted
2024-05-23
Last updated
2024-05-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06426355. Inclusion in this directory is not an endorsement.