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NCT07142187

The Clinical Trial of Electro-thumbtack Needle on Live Birth Rate in Patients With Ovarian Reserve Dysfunction (DOR)

Not yet recruiting NA Last updated 26 August 2025
What this trial tests

NA trial testing electro-thumbtack needle in Diminished Ovarian Reserve (DOR) in 368 participants. Not yet recruiting.

Timeline
1 October 2025
Primary endpoint
30 October 2029
30 October 2029

Quick facts

Lead sponsorHuazhong University of Science and Technology
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment368
Start date1 October 2025
Primary completion30 October 2029
Estimated completion30 October 2029

Drugs / interventions tested

Conditions studied

Sponsor

Huazhong University of Science and Technology

Who can join

Adults 18 to 40, female only, with Diminished Ovarian Reserve (DOR). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will include 246 patients with ovarian reserve dysfunction (DOR), who will be randomly divided into a treatment group and a control group, with 123 patients in each group. The treatment group will receive electro-thumbtack needle treatment, while the control group will receive placebo electro-thumbtack needle treatment. Both groups will receive a treatment course of 3 menstrual cycles. This study evaluates the effect of electrocautery on the live birth rate of patients with DOR.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Diminished Ovarian Reserve (DOR)

Currently open trials in the same condition.

Other Huazhong University of Science and Technology trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07142187.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing