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Clinical Trial

GyneFix IUD Plus LNG-IUS for Adenomyosis

NCT: NCT07680985 · COMPLETED

NCT IDNCT07680985
StatusCOMPLETED
Start Date2023-07-20
Completion2025-12-31
SponsorWenzhou People's Hospital (OTHER)
First posted
Last updated

Brief Summary

Adenomyosis is a common gynecological condition that can cause menstrual pain, heavy menstrual bleeding, anemia, and reduced quality of life. The levonorgestrel-releasing intrauterine system is commonly used as a conservative treatment, but displacement or expulsion of the device may occur, especially in patients with an enlarged uterus or a deep uterine cavity. This study evaluated whether combining an Indomethacin-GyneFix intrauterine device with a levonorgestrel-releasing intrauterine system could improve device stability in patients with adenomyosis. Eligible participants were randomly assigned to receive GyneFix IUD plus LNG-IUS, ring IUD plus LNG-IUS, or LNG-IUS alone. Participants were followed for 6 months after device placement. The main outcome was device displacement or expulsion at 6 months. Other outcomes included menstrual pain, menstrual blood loss, uterine volume, hemoglobin, CA125, adverse events, and treatment acceptance.

Frequently Asked Questions

What is GyneFix IUD Plus LNG-IUS for Adenomyosis?

GyneFix IUD Plus LNG-IUS for Adenomyosis is a clinical trial registered under NCT07680985. Current status: COMPLETED.

What is the status of NCT07680985?

The current status of NCT07680985 (GyneFix IUD Plus LNG-IUS for Adenomyosis) is: COMPLETED.

When did GyneFix IUD Plus LNG-IUS for Adenomyosis start?

GyneFix IUD Plus LNG-IUS for Adenomyosis started on 2023-07-20.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.