Comparison the effect of rectal and oral misoprostol in First Trimester of Pregnancy Induced Abortio
Not Applicable
- Conditions
- induced abortion.other obstetric conditions-not elsewhere classified094-099
- Registration Number
- IRCT2017042533635N1
- Lead Sponsor
- deputy of research and technology of zahedan university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 140
Inclusion Criteria
Including factors: singleton pregnancy ,gravid 2 -4,without cervical dilatation and bleeding or tissue passing,report of IUFD in two sonographys,gestational age below 14 w,BMI Between 19.8-26 kg/m2
Excluding factors:background diseases related with study such as overt DM,chronic Hypertension,SLE,fever or chorioamnionitis signs,using unusual drugs in pregnant women,addiction,...
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complete abortion. Timepoint: during hospitalization. Method of measurement: uterine sonogeraphy.;Incomplete abortion. Timepoint: during hospitalization. Method of measurement: uterine sonogeraphy.;Cervical ripening. Timepoint: during hospitalization and in time of curettage. Method of measurement: passing the number 8 bugie.;Nausia. Timepoint: during hospitalization. Method of measurement: observation and patient expression.;Vomitting. Timepoint: during hospitalization. Method of measurement: observation.;Fever. Timepoint: during hospitalization. Method of measurement: body temperature > 38 c.;Time of drug effect. Timepoint: repetitive visit and patient expression. Method of measurement: observation and examination.
- Secondary Outcome Measures
Name Time Method