Comparison of three treatment methods in incisional pregnancy
Not Applicable
Recruiting
- Conditions
- cesarean scar.
- Registration Number
- IRCT20101227005485N10
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 15
Inclusion Criteria
Definitive diagnosis of incisional pregnancy
Stable hemodynamic status
Absence of severe vaginal bleeding
Consent to participate in the study
Pregnancy less than 10 weeks
Exclusion Criteria
History of drug sensitivity
History of blood disorders
Having liver disorders
Having pulmonary disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of the study is the successful treatment of patients, which is the reduction of serum b-hCG levels until it become negative. Timepoint: Every week. Method of measurement: Radioimmunoassay.;The primary outcome of the study is the successful treatment of patients, by confirming the empty uterus on the ultrasound exam. Timepoint: Every mounth. Method of measurement: Transvaginal sonography.
- Secondary Outcome Measures
Name Time Method