The remains of a pregnancy. Spontaneous abortion : incomplete, without complication
Conditions
Interventions
Intervention 1: We delivered 10 packs 60 grams of sesame to the intervention group and also we trained them How to prepare and use it. For 5 days, twice a day, in the same time misoprostol tablets pre
Treatment - Drugs
We delivered 10 packs 60 grams of sesame to the intervention group and also we trained them How to prepare and use it. For 5 days, twice a day, in the same time misoprostol tablets prescribed by obste
They prescribed misoprostol tablets routinely to the control group by obstetricians.
Sponsors
Vice chacellor for research, Isfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The full disposal of the products of pregnancy. Timepoint: Two weeks after intervention. Method of measurement: Sonography. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Aghababaei
Isfahan University of Medical Sciences
Outcome results
None listed