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Clinical Trial Summary

Transcervical resection of myoma(TCRM) has a good therapeutic effect while the probability of complete resection of type I and II fibroids is only 55% per procedure on average and a significant number of patients have fibroid remained.At present, there is no standardized treatment option for reducing the remaining submucous fibroids volume and preventing its recurrence after TCRM.The present prospective,multicentre,randomised controlled clinical trial will enrol women after TCRM and treat them with mifepristone(10mg)or GnRHa(3.60mg)for 3 to 6 months,investigating the effective and cost-effective treatment options after fibroids with TCRM,thus to provide evidence and effectual regiments for reducing remaining fibroids volume and preventing its recurrence.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05898321
Study type Interventional
Source Women's Hospital School Of Medicine Zhejiang University
Contact WU zaigui
Phone 15957193058
Email 411773@zju.edu.cn
Status Not yet recruiting
Phase N/A
Start date June 1, 2023
Completion date December 30, 2025

See also
  Status Clinical Trial Phase
Completed NCT03930069 - Vasopressin Injection Versus Misoprostol During Hysteroscopic Myomectomy In Reducing Blood Loss And Operation Time. Phase 2/Phase 3