Comparison Between Evening Primrose And Misoprostol On The Cervical Ripening And Dilatation Before Gynecologic Surgeries. Abnormal uterine and vaginal bleeding, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Non-pregnant women without history of normal vaginal delivery,or menopause women, that need cervical dilation before the surgery.Vaginal administration of 2Primros
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 75 Years
Inclusion criteria
Inclusion criteria: Non-menopause women without history of previous normal vaginal delivery Menopause women
Exclusion criteria
Exclusion criteria: Previous Normal Vaginal Delivery Structural Cervical Anomaly such as cervical incompetency Mullerian Anomalies Previous Cervical Conization Contraindications of Misoprostol and Primrose
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total cervical dilatation time. Timepoint: From the first Hegar to the tenth Hegar. Method of measurement: Second.;The first Hegar size used to apply force. Timepoint: During surgery. Method of measurement: Hegar size number.;Blood loss. Timepoint: Estimated blood loss during surgery. Method of measurement: mililiter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Drugs side effects. Timepoint: After administration, 6hand24h. Method of measurement: Observation, Questionaire.;Complications of surgery. Timepoint: During surgry. Method of measurement: Check list. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBehnaz Nouri
Shahid Beheshti University of Medical Sciences
Outcome results
None listed