Skip to content

Control of symptoms of catheter related bladder discomfort by preoperative tramadol,clonidine or pregabalin

Evaluation of preoperative clonidine,pregabalin or tramadol on severity of catheter related bladder discomfort in patients undergoing percutaneous nephrolithotomy - CRBD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/01/007658
Enrollment
160
Registered
2017-01-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients of either sex, 18-60 years of age, ASA grade I & II undergoing elective percutaneous nephrolithotomy under general anaesthesia upto 24 hours postoperatively.

Interventions

Intervention1: Cap .Tramadol100mg: The drug will be filled in identical looking soft gelatin capsule from pharmacy and administered one hour prior to induction with sip of water Intervention2: Cap Pre

Sponsors

Himalayan Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex, 18-60 years of age, ASA grade I & II undergoing elective percutaneous nephrolithotomy under general anaesthesia

Exclusion criteria

Exclusion criteria: Exclusion Criteria - Age 60years - ASA grade III & IV - History of significant cardiac diseases like previous MI, arrhythmias, high A V conduction blocks, uncontrolled hypertension, angina. - History of chronic use of beta- blockers - Sleep apnoea - Significant liver dysfunction - History of chronic opioid use, - Patients with renal failure ( higher serum creatinine levels >= 1.5mg%, urine 3 at night or >8 in 24 hours) / transurethral resection of prostate for benign prostatic hyperplasia -Hypersensitivity to any of the study drugs.

Design outcomes

Primary

MeasureTime frame
Incidence and severity of CRBDTimepoint: Incidence and severity of CRBD at 0hr,30min,2 hrs,4 hrs,6 hrs ,12 hrs & 24 hrs postoperatively

Secondary

MeasureTime frame
Preoperative sedation Haemodynamic variability Adverse effects Amount of postoperative fentanyl required by PCA.Timepoint: Preoperative before induction Intraoperative Postoperatively 24 hours

Countries

India

Contacts

Public ContactSanjay Agrawal

Himalayan Institute of Medical Sciences

samia.kohli99@gmail.com9719529195

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026