Urinary retention. Bladder-neck obstruction
Conditions
Interventions
Intervention 1: Intervention group: Tamsulosin portal 0.4 mg, oral, 3 doses, one day, 6 hours before surgery, during surgery and 6 hours after surgery. Intervention 2: Control group: placebo, 3 doses,
Treatment - Drugs
Intervention group: Tamsulosin portal 0.4 mg, oral, 3 doses, one day, 6 hours before surgery, during surgery and 6 hours after surgery.
Control group: placebo, 3 doses, for a day, 6 hours before surgery, during surgery and 6 hours after surgery.
Sponsors
Vice chancellor for research, Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: All patients under 40 years of age who are referred to Mobinin Hospital in Sabzevar for elective cesarean section Exclusion criteria: Emergency cesarean section; Serum volume received more than 1000 cc before surgery; Pre-eclampsia; age over 40 years; history of neurological disease; history of Gynecologic surgery; preoperative urinary symptoms; Alpha blocker use before the operation
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Urinary retention. Timepoint: After the intervention. Method of measurement: History and volume of urine after catheterization. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hypotension. Timepoint: 24 hours after intervention. Method of measurement: In millimeters of mercury using a mercuric pressure gauge. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamidreza Baghani Aval
Sabzevar University of Medical Sciences
Outcome results
None listed