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NCT05305677Completed

Effect of NMN (Nicotinamide Mononucleotide) on Polycystic Ovary Syndrome

Effect of NMN (Nicotinamide Mononucleotide) Intervention on Patients With Polycystic Ovary Syndrome

Source: ClinicalTrials.gov · Last updated 25 Nov 2025

Brief summary (registry, in English)

The purpose of the study is to understand the effect of Nicotinamide mononucleotide (NMN) on patients with polycystic ovary syndrome.

Status (registry)
Completed
Study type
Interventional
Enrollment
88 (actual)
First submitted
14 Mar 2022
Start date
1 Jun 2022
Primary completion date
31 Dec 2023
Lead sponsor
Peking University Third Hospital
NCT number
NCT05305677

What you commit to

  • Study type: Interventional
  • Participants enrolled: 88
  • From 1 Jun 2022 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Individuals who currently receiving weight-loss drugs or surgery or within the past 2 months.
  • Use of medications that affect hormone levels, appetite, carbohydrate absorption, and metabolism within the past 2 months.

Other illness

  • Individuals who suffering from other diseases that may cause hyperandrogenism and ovulation abnormalities.
  • Individuals who need regular medication to treat chronic diseases such as diabetes, hypertension, gout, hyperuricemia, etc.
  • Individuals with severe liver diseases or kidney disease that are ineligible to participate in the study.
  • A medical history of severe cardiovascular and cerebrovascular diseases.
  • Individuals who currently suffer from severe gastrointestinal diseases or undergo gastrointestinal resection that may affect nutrient absorption.
  • Individuals who need drug treatment for any mental illness such as epilepsy and depression.
  • Cancer patients.
  • Individuals who suffer from infectious diseases such as hepatitis B, active tuberculosis, AIDS, etc.

Other

  • Individuals who are during pregnant, lactation or menopause.
  • Individuals who take niacin, nicotinamide, or other vitamin B-related supplementation currently or within the past 2 months.
  • Individuals who drink more than 15g of alcohol per day or have a smoking habit.

Who the study is looking for

  • Individuals who are 20 to 40 years old;
  • BMI \< 25 kg/m2;
  • Individuals with PCOS should meet all the Rotterdam diagnostic criteria: 1) Oligo- and/or anovulation; 2) Clinical and/or biochemical signs of hyperandrogenism; 3) Polycystic ovaries, and exclusion of other aetiologies (congenital adrenal hyperplasia, androgen-secreting tumors, Cushing's syndrome).
  • Individuals who can insist on continuous monitoring in the outpatient clinic.
  • Individuals who are not participating in other research projects currently or 3 months before the intervention.

Age in the registry: 20 years to 40 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University Third Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.