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The Effect of Dihydroartemisinin in PCOS

The Evaluation of the Effect of Dihydroartemisinin in Patients With Polycystic Ovary Syndrome

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05465135
Enrollment
19
Registered
2022-07-19
Start date
2022-07-01
Completion date
2023-04-23
Last updated
2024-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome

Brief summary

Artemisinin has been widely used as a first-line antimalarial drug in routine clinical practice. In recent years, it has been reported that Artemisinin also has some significant anti-inflammatory, anti-tumor and immune-modulating effects. The investigators' previous studies discovered that Artemisinin dramatically reduced serum androgen levels and improved poly-cystic ovary syndrome(PCOS) in animals. Preliminary study by the investigators found that artemisinin derivatives are capable of reducing both androgen levels and improving insulin resistance, two clinical characteristics of PCOS. Thus artemisinin derivatives has the potential effect to alleviate PCOS symptoms. The current study aims to investigate the effect of artemisinin on improving PCOS and serum androgen levels in PCOS subjects.

Detailed description

Polycystic ovary syndrome (PCOS) is a common reproductive endocrine metabolic disorder caused by a combination of genetic and environmental factors. The pathogenesis of PCOS remains unclear. Artemisinin has been widely used as a first-line antimalarial drug in routine clinical practice. In recent years, it has been reported that Artemisinin has significant anti-inflammatory, anti-tumor and immune-modulating effects. The investigator's previous studies found that artemisinin and its derivatives could significantly promote uncoupling protein 1 (UCP1) transcription and the conversion of white fat to brown fat. Artemisinin derivatives upregulated the levels of genes critical for brown fat differentiation and function, accompanied by enhanced mitochondrial biosynthesis, demonstrating their potential to promote white fat browning and improve metabolism in rodent models. The investigators also observed that androgen levels in drug-induced PCOS rats were reduced, when treated with artemether analogs for prophylactic and therapeutic purposes, respectively. It is believed that the two core mechanisms in the pathogenesis of PCOS are excessive androgen synthesis and insulin resistance. Preliminary study by the investigators found that artemisinin derivatives are capable of reducing both serum androgen levels and improving insulin resistance, two clinical characteristics of PCOS. Thus artemisinin derivatives has the potential effect to alleviate PCOS symptoms and control or even reverse the disease progression. The current study aims to investigate the effect of artemisinin on improving PCOS and serum androgen levels in PCOS subjects.

Interventions

Dihydroartemisinin 40mg three times a day for 12 consecutive weeks.

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

20 participants with PCOS receive dihydroartemisinin for 3 months

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* BMI 23-30kg/M2 * No plan for pregnancy in the coming 6 months * Newly diagnosed PCOS, or PCOS without any medication for the past three months. * Patients should meet all the three following criteria: 1. Oligomenorrhea or amenorrhea: Oligomenorrhea is defined as more than 35 days between menstrual periods and less than 8 menstrual bleedings in the past year; amenorrhea is defined as more than 90 days between two menstrual bleedings. 2. Polycystic ovaries: ≥12 follicles in both ovaries (diameter\<10mm), confirmed by ultrasound. 3. Elevated androgen levels: testosterone\>1.67 nmol/L.

Exclusion criteria

* Previously treated with steroids or other medications for PCOS in the past 3 months. * Patients with other endocrine diseases that can cause secondary PCOS, including but not limited to: 21 hydroxylase deficiency, prolactinoma, hypothyroidism, Cushing's syndrome, etc. * Pregnancy. * Patients with other serious diseases affecting heart, liver, kidney, or other major organs. * Patients with any type of cancer.

Design outcomes

Primary

MeasureTime frameDescription
Recovery of regular menses by questionnaire12 weeksPeriodical vaginal bleeding by questionnaire
Bilateral ovary volume12 weeksLength, width and height of bilateral ovaries measured by B type ultrasound
Number of immature follicles12 weeksTotal number of follicles with diameters \<10 mm measured by B type ultrasound
Serum testosterone levels12 weeksMeasurement of serum total testosterone

Secondary

MeasureTime frameDescription
Sex hormone binding globulin (SHBG)12 weeksMeasurement of serum SHBG
Serum dehydroepiandrosterone sulfate12 weeks after drug interventionMeasurement of serum DHEA
Serum anti-Mullerian hormone12 weeksMeasurement of serum AMH

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026