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Dexmedetomidine instilled in urinary bladder for prevention of post-operative catheter related bladder discomfort in renal transplant patients.

Intravesical Dexmedetomidine for prevention of post-operative catheter related bladder discomfort in renal transplant recipients- a prospective randomized double-blind, placebo-controlled study. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056908
Enrollment
90
Registered
2023-08-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: N186- End stage renal disease

Interventions

Intervention1: Dexmedetomidine group: 2.5ug/kg dexmedetomidine in 100ml Normal Saline will be introduced once via Foleys catheter before the surgery begins. The catheter will then be clamped for 30-40

Sponsors

Sanjay Gandhi Postgraduate Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: End Stage Renal Disease patients about to undergo Renal Transplant Surgery.

Exclusion criteria

Exclusion criteria: Patients with history of outflow obstruction, transurethral resection of prostate for benign prostatic hyperplasia, history of bladder catheterization within last 6 months, re look Percutaneous Nephrolithotomy, Pre-existing percutaneous nephrostomy , overactive bladder (frequency >3 times in the night or >8 times in 24 h), morbid obesity, disturbance of the central nervous system, chemical substance abuse or any psychiatric disease.

Design outcomes

Primary

MeasureTime frame
Incidence of Cathedral Related Bladder Discomfort (CRBD) in each group.Timepoint: 2 hours post surgery

Secondary

MeasureTime frame
Incidence of Cathedral Related Bladder Discomfort (CRBD) in each group.Timepoint: 0, 4, 12 & 24 hours post surgery.;Severity of CRBDTimepoint: 0,2,4,12,and,24 hours post surgery.;Incidence of postoperative nausea vomiting (PONV)Timepoint: 0,2,4,12 & 24 hours post surgery

Countries

India

Contacts

Public ContactDivya Srivastava

Sanjay Gandhi Post Graduate Institute of Medical Sciences

dr.divshri@gmail.com07839098150

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026