se of Alginate Carboxymethylcellulose Hyaluronic Acid for Prevention of Intrauterine Adhesion after Vacuum Aspiration in Patients with First Trimester Abortion: A Prospective study
Phase 3
Recruiting
- Conditions
- Abortion
- Registration Number
- TCTR20200314005
- Lead Sponsor
- Ramathibodi hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 68
Inclusion Criteria
- Pregnant woman with gestational age of 13 weeks or less with blighted ovum or incomplete abortions or inevitable abortions or embryonic death with manual vacuum aspiration or electric vacuum aspiration following abortion in outpatient department or inpatient department or emergency department
- No history of uterine curettage, pelvic infection, intrauterine surgery, IUD used, and endometriosis
- Not allergy to Hyaluronic acid, Carboxymethylcellulose or Alginate
Exclusion Criteria
- Need to D&C after the procedure
- Hormonal contraception used during the research period
- Pregnant before the scheduled of hysteroscopy
- Complication during or after the procedure such as uterine perforation, infection, or incomplete abortion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Formation of IUAs 2-3 months Hysteroscopy
- Secondary Outcome Measures
Name Time Method Severity of IUAs 2-3 months Hysteroscopy