NMN Supplementation for IVF Failure Patients
NMN capsule
+ Placebo
Urogenital Diseases+4
+ Genital Diseases
+ Female Urogenital Diseases and Pregnancy Complications
Basic Science Study
Summary
Study start date: August 20, 2024
Actual date on which the first participant was enrolled.This clinical study focuses on improving the chances of success for people undergoing in vitro fertilization (IVF) who have faced previous failures. It investigates the use of a compound called Nicotinamide mononucleotide (NMN), which has shown promise in enhancing the quality of eggs in older individuals by supporting energy production and reducing cellular damage. The study is important because recurrent IVF failures can have significant emotional and financial impacts, and finding effective ways to improve egg quality may enhance the success rate of these fertility treatments. Participants in this study will take part in a trial where they are randomly assigned to receive either the NMN supplement or a placebo, without knowing which one they are getting, to ensure unbiased results. The supplement is given orally in a daily dose of 900 mg. Researchers will monitor the effects of NMN on IVF outcomes by evaluating the quality of eggs and embryos. The study aims to determine if NMN can indeed improve the chances of successful fertilization and pregnancy for those who have previously experienced challenges with IVF.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 32 to 42 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
Active ComparatorGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
IVF Namba Clinic, Sankaky Medical Corporation
Osaka, JapanOpen IVF Namba Clinic, Sankaky Medical Corporation in Google Maps