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The Effect of Coenzyme Q10 Pretreatment on Ovarian Reserve in Women Undergoing Hysterectomy with Bilateral Salpingectomy: A Randomized, Double-Blind, Placebo-Controlled Trial

The Effect of Coenzyme Q10 Pretreatment on Ovarian Reserve in Women Undergoing Hysterectomy with Bilateral Salpingectomy: A Randomized, Double-Blind, Placebo-Controlled Trial

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230926003
Enrollment
44
Registered
2023-09-26
Start date
2022-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

the ovarian reserve change using anti-mullerian hormone levels before and 6 weeks after undergoing hysterectomy with bilateral salpingectomy ovarian reserve anti-mullerian hormone hysterectomy Coenzyme Q10

Interventions

oral 300 mg of Coq10 supplement for two weeks before undergoing hysterectomy with bilateral salpingectomy,The placebo was an identical soft gelatin capsule as the intervention arm. oral placebo was g
Placebo Comparator Drug,Placebo Comparator Drug
CoQ10,placebo

Sponsors

Ramatibodi hospital, Mahidol university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. The women age between 25 to 45 years old 2. Diagnosed with leiomyoma or adenomyosis scheduled for hysterectomy with bilateral salpingectomy 3. Provided signed informed consent

Exclusion criteria

Exclusion criteria: 1. History of ovarian surgery 2. Anticipated ovarian cystectomy 3. Hormonal use within 3 months before surgery 4. Known allergies to CoQ10 or starch 5. Suspected malignancy 6. Drug use that interacts with CoQ10 , for example; warfarin or statin

Design outcomes

Primary

MeasureTime frame
percentage AMH change 2 weeks before surgery and 6 weeks after surgery percentage AMH change between pre- and post-operative level

Secondary

MeasureTime frame
safety profile after two weeks course of intervention or placebo side effects report by participants,Liver and renal function 6 weeks after complete course of intervention or placebo SGOT, SGPT, BUN, creatinine levels

Countries

Thailand

Contacts

Public ContactArtitaya Singwongsa

Reproductive Endocrinology and Infertility Unit, Department of Obstetrics and Gynaecology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

artitaya@me.com66900436303

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026