Overview
Efficacy of Hyoscine-n-butylbromide in Catheter-related Bladder Discomfort After Elective Cesarean Section.
Status:
Unknown status
Unknown status
Trial end date:
2018-07-15
2018-07-15
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
a prospective, randomized, placebo-controlled study will be conducted to investigate whether hyoscine-n-butylbromide has preventive effects on early postoperative CRBD in patients with urinary catheters who will undergo elective cesarean sections.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Cairo UniversityTreatments:
Butylscopolammonium Bromide
Scopolamine
Scopolamine Hydrobromide
Criteria
Inclusion Criteria:- Elective primary or repeat cesarean section more than 37 weeks of gestation scheduled
to insert a Foley catheter in the operation site.
- The absence of significant vaginal bleeding
Exclusion Criteria:
- • Urinary infection (assessed clinically and by urinalysis of midstream sample of
urine (MSSU) with chemical indicator strips or dipsticks).
- Contraindications for general anesthesia.
- Maternal bladder, urethral and renal disorders causing irritating voiding
problems such as dysuria, urge and stress incontinence.
- Obstructive voiding symptoms like incomplete emptying, straining and voiding
difficulty before surgery.
- Overactive bladder (frequency: more than three times during the night or more
than eight times in 24 h).
- Morbid obesity.
- Disturbances of the central nervous system (epilepsy, patients receiving MAO
inhibitor).
- Hypertensive disorders and/ or systemic disease requiring particular patient care
(for example, cardiac disease, nephritic disorders).
- Chronic analgesic abuse.
- Hepatic or psychiatric disease will be excluded from the study.
- A history of hypersensitivity or contraindication to hyoscine-n-butylbromide.