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A RESEARCH ABOUT THE PAIN RELIEVING EFFECT OF THE MEDICINE, GABAPENTIN, WHEN GIVEN BEFORE SURGERY, IN THE CASE OF UTERUS REMOVAL OPERATION DONE UNDER SPINAL ANAESTHESIA

A STUDY ON THE EFFECT OF PRE-EMPTIVE ANALGESIA WITH GABAPENTIN ON POST-OPERATIVE PAIN RELIEF AFTER TOTAL ABDOMINAL HYSTERECTOMY UNDER SUBARACHNOID BLOCK

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/06/004674
Enrollment
60
Registered
2014-06-13
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- Female Patients undergoing Total Abdominal Hysterectomy

Interventions

Intervention1: Gabapentin: Gabapentin 300mg, Oral, single dose, 2 hours before surgery Control Intervention1: PLACEBO (B Complex): PLACEBO (B Complex), One tablet, Single dose, 2 hours before surgery

Sponsors

Robert James Premkumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade I and II undergoing Total Abdominal Hysterectomy

Exclusion criteria

Exclusion criteria: Denial of consent, Allergy to Gabapentin, Consumption of NSAID in last 48 hrs, Patients Suffering from epilepsy, liver disease, renal disease, chronic pain syndrome, Patients who have psychiatric illness

Design outcomes

Primary

MeasureTime frame
VISUAL ANALOGUE SCALE Pain ScoreTimepoint: 2, 4, 8, 12, 24 Hours after surgery—

Secondary

MeasureTime frame
The amount of rescue analgesic consumptionTimepoint: 0-2, 2-4, 4-8, 8-12, 12-24 Hours after Surgery—

Countries

India

Contacts

Public ContactRobert James Premkumar

Dr SMCSI Medical College

robertjamespk@hotmail.com09443352633

Outcome results

None listed

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