Abortion. Miscarriage
Conditions
Interventions
Intervention 1: In case group vaginal administration of isonicotinic
acid hydrazide (INH) (1800mg) + misoprostol (800 mg sublingual 8hrs later) which will be repeated every 3hrs upto 3times in 12hours
Treatment - Drugs
In control group 800 mcg sublingual misoprostol given that in the absence of pain and vaginal bleeding occurs every three hours. (Maximum of three doses in 12 hours)
In case group vaginal administration of isonicotinic
acid hydrazide (INH) (1800mg) + misoprostol (800 mg sublingual 8hrs later) which will be repeated every 3hrs upto 3times in 12hours in as needed.
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: All pregnant women with gestational age less than or equal to 91 days based on sonography and lmp that refereed to Akbar Abadi hospital and were candidates for the termination of pregnancies (blighted ovum, missed abortion) or medical abortion license included this study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abortion time. Timepoint: During the intervention. Method of measurement: Hour. | — |
Secondary
| Measure | Time frame |
|---|---|
| Vomiting. Timepoint: During the intervention. Method of measurement: Visual Analogue Scale.;Diarrhea. Timepoint: During the intervention. Method of measurement: Visual Analogue Scale.;Fever. Timepoint: During the intervention. Method of measurement: Celsius degrees.;Nausea. Timepoint: During the intervention. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Ladan Haghighi
Iran University of Medical Science
Outcome results
None listed