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A comparative study between oral gabapentin and oral pregabalin in acute post-operative pain management in patients undergoing urological procedures under sub-arachnoid block.

A comparative study of oral gabapentin versus oral pregabalin in acute post-operative pain management in patients undergoing urological procedures under sub-arachnoid block. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073892
Enrollment
66
Registered
2024-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: N29- Other disorders of kidney and ureter in diseases classified elsewhere Health Condition 2: N288- Other specified disorders of kidney and ureter

Interventions

Intervention1: Adminstration of Gabapentin: Administration of T. Gabapentin 600 mg orally 1 hour before administration of anaesthesia Control Intervention1: Gabapentin: Administration of Gabapentin 1

Sponsors

Sapthagiri Institute of Medical Sciences and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients willing to give written informed consent. 2. Patients undergoing urological procedure. 3. ASA grade - 1&2

Exclusion criteria

Exclusion criteria: 1. ASA Grade - 3 & above. 2. Patients with known allergy to pregabalin, history of intake of NSAIDs within 48 hours of surgery, coagulation abnormalities. 3. Patients on anti-coagulant and anti-platelet medications.

Design outcomes

Primary

MeasureTime frame
VAS scoreTimepoint: VAS score assessed at baseline, 2, 4, 6 and 12 hours after procedure.

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactNarendra Babu C

Sapthagiri Institute of Medical Sciences and Research Institute

narendrababuchanappa@gmail.com9900214064

Outcome results

None listed

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