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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-40
SponsorPeking University Third Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Individuals who are 20 to 40 years old.

The concentrations of anti-Mullerian hormone < 1.1 ng/ml,

the values of antral follicle count was less than 7

serum concentrations of day-3 follicle-stimulating hormone (FSH): 10 IU/L ≤ FSH<20 IU/L

Disqualifiers

Individuals who are during pregnant, lactation or menopause.

Individuals who had non-46-XX karyotype, or attributed to known genetic etiology.

Cancer patients or receiving chemo/radiotherapy treatment within the past 5 years.

Individuals who need regular medication to treat chronic diseases such as diabetes, hypertension, gout, hyperuricemia, etc.

Trial design

Treatments tested in this trial

  • NMN
  • Placebo

Treatment groups

200 Participants
are divided into 2 treatment groups