Comparison of the effect of misoprostol and isosorbide mononitrate on cervix.
Conditions
Interventions
Intervention 1: Intervention group received 25 µg misoprostol (vaginal every 4 hours to 4 doses). Intervention 2: Control group: 60 mg isosorbine mononitrate suppository every 6 hours until two doses.
Sponsors
Zabol University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: infertile wemen undergoing histroscopy
Exclusion criteria
Exclusion criteria: This study is conducted on infertile women undergoing hysteroscopic surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study of headache after taking misoprostol and isosorbide mononitrate on cervix. Timepoint: Headache in the beginning of the study after taking Misoprostol and isosorbide mononitrate on the cervix. Method of measurement: Asking questions from the patient himself.;Study of nausea and vomiting after taking misoprostol and isosorbide mononitrate on cervix. Timepoint: Nausea and vomiting at the beginning of the study following the use of Mizo, Prostol and Isosorbide Mononitrate on the cervix. Method of measurement: Asking questions from the patient himself.;Evaluation of abdominal pain after taking misoprostol and isosorbide mononitrate on the cervix. Timepoint: ??Abdominal painat the beginning of the study following the use of Mizo, Prostol and Isosorbide Mononitrate on the cervix. Method of measurement: Asking questions from the patient himself.;Evaluation of cervical dilatation after taking misoprostol and isosorbide mononitrate. Timepoint: Study of cervical dilatation rate at the beginning of study after misoprostol and isosorbide mononitrate. Method of measurement: Respectively, using small to large bogies. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Shahraki
Zabol University of Medical Sciences
Outcome results
None listed