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Optimal duration of bladder catheterization after elective caesarean section to prevent urinary tract morbidity: a randomized controlled trial of 12 versus 24 hours. - Trial PACTR202308564052985

Access comprehensive clinical trial information for PACTR202308564052985 through Pure Global AI's free database. This Not Applicable trial is sponsored by Dr Loretta Nnakwe and is currently Recruitment Completed. The study focuses on Obstetrics and Gynecology.

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PACTR202308564052985
Not Applicable
Recruitment Completed
Trial Details
Pan Africa Clinical Trials Registry โ€ข PACTR202308564052985
Pure Global
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Optimal duration of bladder catheterization after elective caesarean section to prevent urinary tract morbidity: a randomized controlled trial of 12 versus 24 hours.

Study Focus

Obstetrics and Gynecology

Sponsor & Location

Dr Loretta Nnakwe

Nigeria

Timeline & Enrollment

Not Applicable

Jan 01, 1900

Jan 01, 1900

Summary

The rate of caesarean section has been on the rise worldwide due to its ability to prevent maternal and foetal morbidity and mortality. However, bladder catheterization during caesarean section can result in urinary tract morbidities. The optimal duration before removal of the catheter after caesarean section remains contentious and current practice is rather customary than global best practice guideline. The aim of this trial is to compare the post-operative morbidities associated with either 12-hour or 24-hour duration of bladder catheterization after elective caesarean section. Specific objectives include the prevalence of urine retention, significant bacturiuria, urinary tract infection and the pattern of post-operative recovery between both groups.

ICD-10 Classifications

Obstetric and gynaecological devices associated with adverse incidents
Obstructed labour due to other maternal pelvic abnormalities
Obstetric and gynaecological devices associated with adverse incidents : miscellaneous devices, not elsewhere classified
Obstetric and gynaecological devices associated with adverse incidents : diagnostic and monitoring devices
Other complications of obstetric surgery and procedures

Data Source

Pan Africa Clinical Trials Registry

PACTR202308564052985

Non-Device Trial