UnknownNot Applicable

Three-dimensional Ultrasound Applying in Assessment of Intrauterine Adhesions

China600 participantsStarted 2020-07-01

Plain-language summary

In this prospective, multicenter, large-scale study，the investigators wish to examine the accuracy of several three-dimensional ultrasound anatomical and vascular parameters in diagnosing IUA when compared to the gold standard of hysteroscopy，and to assess the value of 3D US applying in prognosis of intrauterine adhesions.

Who can participate

Age range

20 Years – 40 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * women aged 20-40 * oligomenorrhea or amenorrhea * BMI 18-30 * regular menstruation * written consent obtained Exclusion Criteria: * Hypothalamic amenorrhea, pituitary amenorrhea and ovarian amenorrhea * Patients with uterine fibroids, adenomyosis, uterine malformation and endometrial polyps * Patients with uterine artery embolization * History of endometrial hyperplasia * Irregular menstruation * Patients with severe complications * Patients with hypoovarian function

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Endometrial volume

Timeframe: 1 year

Trial details

NCT IDNCT04930913

SponsorFu Xing Hospital, Capital Medical University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2022-06-30

Contact for this trial

Huang xiaowu

+8613810828816 hxiaowu_fxyy@126.com

View on ClinicalTrials.gov More Intrauterine Adhesion trials