Het voorkomen van littekenvorming in de baarmoeder bij vrouwen die een curettage ondergaan vanwege een miskraam. (Evaluatie van anti-verklevingsmiddel).
Recruiting
- Registration Number
- NL-OMON22431
- Lead Sponsor
- Sint Lucas Andreas ziekenhuis
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
Consented patients, who had at least one previous suction or abrasive (blunt or sharp) curettage for a miscarriage in the history, visiting the outpatient clinic with a miscarriage and planned for curettage, will be included in the study. The ultrasound is a key in the diagnosis of miscarriage; at least one recent ultrasound examination (made within 7 days before randomisation) is required for inclusion. The maximum gestational age at inclusion is 14 weeks.
Exclusion Criteria
1. Patients with a suspected mola pregnancy;
2. Patients with a previous hysteroscopic surgery (endometrial ablation, removal of fibroids or surgical correction of congenital uterine anomalies);
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure is number of patients with intra-uterine adhesions during the follow-up hysteroscopy.
- Secondary Outcome Measures
Name Time Method 1. Severity of intra-uterine adhedsions (IUAs);<br /><br>2. Time to conceive during one year;<br /><br>3. Number and time to clinical pregnancy during one year;<br /><br>4. Number and time to ongoing pregnancy during one year;<br /><br>5. Number of miscarriages during the first year after curettage.