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Efficacy of Warm Irrigation Solution in Improving Perioperative Outcomes in Patients Undergoing Transurethral Resection of Prostate

Efficacy of Warm Irrigation Solution in Improving Perioperative Outcomes in Patients Undergoing Transurethral Resection of Prostate: A Prospective Parallel Arm Single Blinded Randomized Control Trial. - WIPOT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045235
Enrollment
54
Registered
2022-09-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms Health Condition 2: N401- Benign prostatic hyperplasia withlower urinary tract symptoms

Interventions

Intervention1: Warm saline irrigation (heated to body temperature i.e 37ºC): Patients will receive warm saline irrigation (heated to body temperature i.e 37ºC) during the intraoperative period. Contro

Sponsors

AIIMS Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consented cases of 1-patients aged =18 years. 2-patients with benign prostatic hyperplasia with any one of the following: i. Lower urinary tract symptoms who had failed standard medical therapy (alpha blockers, 5 alpha reductase inhibitors) ii. Recurrent urinary retention (drug-refractory) iii. Recurrent urinary tract infection iv. Recurrent hematuria v. Obstructive uropathy

Exclusion criteria

Exclusion criteria: 1 ASA Grade 3 or more. 10 2 Patients with congenital or acquired Hyper/ hypocoagulation disorders. 3 Patients with hematological malignancies. 4 Patients with decompensated chronic liver disease or renal impairment or other bleeding diathesis. 5 Patients with collagen vascular disease or other connective tissue disorders. 6 Patients with a history of thromboembolic disease. 7 Patients with history of arrhythmias 8 Patients with a history of acute coronary syndrome within the past 12 months 9 Patients with active or untreated UTI

Design outcomes

Primary

MeasureTime frame
intra-operative blood lossTimepoint: intra-operatively

Secondary

MeasureTime frame
efficacy of resection of TURP surgery. (assessed by weight of resected tissue/ resection time)Timepoint: immediate Postoperatively;incidence of hypothermiaTimepoint: intra-operatively;mean postoperative pain scoreTimepoint: in recovery room, at 6h, at 24h;rates of postop infection/UTI (fever, WBC count, Urine C/S).Timepoint: At 48 hours

Countries

India

Contacts

Public ContactKirti Singh

AIIMS Bhubaneswar

urol_manoj@aiimsbhubaneswar.edu.in7894453494

Outcome results

None listed

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