Role of Chronic Endometritis in Postoperative Recurrence of Severe Intrauterine Adhesions (NCT02744807) | Clinical Trial Compass
CompletedNot Applicable
Role of Chronic Endometritis in Postoperative Recurrence of Severe Intrauterine Adhesions
125 participantsStarted 2015-05
Plain-language summary
This study is to evaluate the prevalence of chronic endometritis (CE) in women with severe intrauterine adhesions and compare recurrence of adhesion in women with and without CE.
Who can participate
Age range20 Years – 40 Years
SexFEMALE
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Inclusion Criteria:
* Pre-operative adhesion score was ≥5
* The prior menstrual cycle was regular, and the sex hormone was normal
* with informed consent
* absence of other uterine abnormality at transvaginal ultrasound
* There were no severe systemic diseases, and no contradictions to aspirin, estrogen and surgery.
Exclusion Criteria:
* Pre-operative adhesion score was \<5
* Prior menstrual cycle was irregular and sex hormone was abnormal, or patients had endocrine factors that caused amenorrhea, menstrual reduction and infertility
* other uterine abnormality at transvaginal ultrasound
* without informed consent
* Patients had contradictions to estrogen and aspirin such as cancers (breast cancer and endometrial cancer), thrombotic diseases, allergy to antipyretic analgesics, severe liver injury, hypoprothrombinemia, vitamin K deficiency, hemophilia, thrombocytopenia, gastric or duodenal ulcer and asthma
* refuse Endometrial biopsy
* Vaginal discharge abnormal, or Suspected vaginitis or pelvic inflammatory disease, or using antibiotics.
What they're measuring
1
Number of Participants With recurrence of adhesion in women with and without Chronic endometritis
Timeframe: 1 year
Trial details
NCT IDNCT02744807
SponsorFirst Affiliated Hospital, Sun Yat-Sen University