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NCT06417099CompletedPhase 2

Efficacy of Dihydroartemisinin for Treating PCOS

Therapeutic Efficacy of Dihydroartemisinin in Patients With Polycystic Ovary Syndrome

Source: ClinicalTrials.gov · Last updated 23 Apr 2025

Brief summary (registry, in English)

The primary research hypothesis of this study is that dihydroartemisinin is effective in restoration of regular menstrual cycles of PCOS subjects who meet at least two of three Rotterdam Criteria. Secondary research hypotheses include: dihydroartemisinin is also effective in reducing androgen, total immature follicles, and anti-Mullerian hormone.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (actual)
First submitted
12 May 2024
Start date
24 May 2024
Primary completion date
30 Mar 2025
Lead sponsor
Shanghai Zhongshan Hospital
NCT number
NCT06417099

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 30
  • From 24 May 2024 to the primary completion date, 30 Mar 2025
  • 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.

Other illness

  • Patients with other endocrine diseases that can cause secondary PCOS, including but not limited to: 21 hydroxylase deficiency, prolactinoma, hypothyroidism, Cushing's syndrome, etc.
  • Patients with other serious diseases affecting heart, liver, kidney, or other major organs.
  • Patients with any type of cancer.

Other

  • Pregnancy.

Who the study is looking for

  • BMI 18.5-28kg/M2
  • No plan for pregnancy in the coming 6 months
  • Patients should meet two of the three following criteria:
    • Irregular cycles and ovulatory dysfunction: \< 21 or \> 35 days or \< 8 cycles per year; \> 90 days for any one cycle
    • Polycystic ovaries: ≥12 follicles in at least one of two ovaries (diameter\<10mm), confirmed by ultrasound.
    • Elevated androgen levels: total testosterone\>1.67 nmol/L.

Age in the registry: 18 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
Zhongshan Hospital,Fudan University
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

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