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A clinical trial to study the safety and practicability of mono polar urethral route removal of prostate without post-surgery urinary catheter traction in patients with enlarged prostate

A randomized control trial to evaluate the safety and feasibility of mono polar transurethral resection of prostate without post-operative urethral catheter traction in benign prostatic hyperplasia patients in a teritary care institute

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039199
Enrollment
60
Registered
2022-01-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: not applying traction in post operative patients of transurethral resection of prostate: All the patients in the no traction group will be carefully observed for gross hematuria. If any

Sponsors

Abhineeth K P
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: prostate size of 30-80 ml

Exclusion criteria

Exclusion criteria: 1) Patients refusing to participate/give consent. 2) Patients failed to achieve Intraoperative hemostasis. 3) Patients with both BPH and bladder tumor 4) Patients with both BPH and bladder stone 5) Patients with both BPH and Urethral stricture disease 6) Patients with both BPH and meatal stenosis

Design outcomes

Primary

MeasureTime frame
1) To compare pain scores 2) to compare the post operative blood lossTimepoint: 1) pain scores - using visual analogue score will be recorded at 6 hour,12 hour and 18 hour post surgery 2) Blood loss will be calculated using Bourkeâ??s formula , preopertaive hematocrit and postoperative hematocrit will be evaluated at post operative day one.

Secondary

MeasureTime frame
1.To compare the duration of hospital stay. 2.To compare the incidence of bladder washouts and clot retention. 3.To compare the incidence of deep venous thrombosis Timepoint: 1)Duration of hospital stay. (Calculated from the day of surgery to day of discharge) 2)The incidence of bladder washouts and clot retention 3)The incidence of deep vein thrombosis

Countries

India

Contacts

Public ContactAbhineeth K P

All India Institute of Medical sciences ,bhopal

manoj.urology@aiimsbhopal.edu.in9675480523

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 6, 2026