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A COMPARATIVE STUDY OF Preoperative ANALGESIC EFFICACY OF ORAL GABAPENTIN 600mg VERSUS ORAL PREGABALIN 75mg FOR ORTHOPEDIC SURGERY UNDER SPINAL ANAESTHESIA

A COMPARATIVE STUDY OF PREEMPTIVE ANALGESIC EFFICACY OF ORAL GABAPENTIN 600mg VERSUS ORAL PREGABALIN 75mg FOR ORTHOPEDIC SURGERY UNDER SPINAL ANAESTHESIA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017050
Enrollment
35
Registered
2019-01-11
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: O- Medical and Surgical

Interventions

Intervention1: Gabapentin: gabapentin 600mg ,single dose, oral route Control Intervention1: Oral pregabalin: pregabalin 75mg,single dose, oral route

Sponsors

Department Of Anaesthesia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient age between 18 â?? 60 years. 2.ASA physical status 1 and 2. 3.Patient undergoing lower limb surgery under spinal anaesthesia.

Exclusion criteria

Exclusion criteria: 1.Age 60 years. 2.ASA physical status 3 and above. 3.Patients not giving consent. 4.History of psychiatric illness,pregnancy, 5.anticipated difficult intubation. 6.Patient on drugs that affect central nervous system. • Patient on chronic pain treatment. • Patient sensitive / allergic to local anesthetic agents. • Patients with peripheral sensorineural deficit. • Patients with altered coagulation profile or having bleeding disorder. • Signs of infection at puncture site for spinal anaesthesia.

Design outcomes

Primary

MeasureTime frame
1.Duration of analgesia.Timepoint: From onset of sensory block to VAS more than 3 or patient demanded for rescue analgesia.

Secondary

MeasureTime frame
1. Total dose of rescue analgesic in first 24 hours. 2. Intra-operative Hemodynamic change. 3. Various side effects: Nausea, vomiting, dizziness, sedation, drowsiness and visual disturbances Timepoint: 6 months

Countries

India

Contacts

Public ContactNEENA JAIN

Rajasthan University of health sciences, Jaipur, Rajasthan

drneenaj@gmail.com

Outcome results

None listed

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