Analyze the effect of the sesamum indicum on disposal of the pregnancy remains.
- Conditions
- The remains of a pregnancy.Spontaneous abortion : incomplete, without complication
- Registration Number
- IRCT2016122729062N1
- Lead Sponsor
- Vice chacellor for research, Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion criteri:
1 - Pregnant women 18_50 years pld admitted to Moheb Yas women hospital of Tehran, less than 20 weeks gestational age and with clinical or ultrasound evidence of incomplete abortion.
2 - Lack of infectious abortion’s signs (a) 38 degrees fever or more (b) INDEX (c) 3 degrees fever per hour or more in the first 24 hours.
3 - Lack of any signs of Induced abortion and manipulation by the patient.
4 - Lack of repeated abortion (RPL) due to anatomical disease of mother (Septate Uterus, Unicorns uterus, short Cervix) and diagnosed chromosomal disorders of parents leading to fetal death or blighted ovum and fetal abnormalities including Malformation and Dysmorphic Show, Monosomy X.
5 -The risk of any base disease (Diabetes - blood pressure - kidney failure - heart and liver illness).
6 - Lack of signs of hemorrhagic shock Grade 1(Bleeding more than 750 cc).
7 - Lack of ectopic pregnancy.
8 - Lack of open cervical in examination.
Exclusion criteria:
1 - The emergence of allergies to sesame or its components.
2 - Severe abdominal pain that require emergency intervention.
3 - Fever over 38 degrees.
4 - Sepsis that require antibiotic treatment or abortion.
5 - Severe bleeding (bleeding more than 750 CC).
6 - Unwillingness to continue cooperation.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The full disposal of the products of pregnancy. Timepoint: Two weeks after intervention. Method of measurement: Sonography.
- Secondary Outcome Measures
Name Time Method Amount of bleeding. Timepoint: During the intervention. Method of measurement: PBAC questionnaire.;The time of bleeding stop. Timepoint: Daily medication and the end of the second week. Method of measurement: PBAC questionnaire.;Amount and intensity of pain. Timepoint: Daily medication and the end of the second week. Method of measurement: VAS questionnaire.;Amount of painkiller. Timepoint: Daily medication and the end of the second week. Method of measurement: Researcher questionnaire.;The incidence of misoprostol’s effects. Timepoint: Daily medication and the end of the second week. Method of measurement: Researcher questionnaire.