ConditionDiminished Ovarian Reserve
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 groupsSponsors and collaborators
Source ClinicalTrials.gov