COMPARISON BETWEEN TWO DIFFERENT DOSES (300MG AND 600MG) OF THE DRUG GABAPENTIN TO ASSESS POST OPERATIVE PAIN TOLERANCE OF PATIENTS UNDERGEOING LOWER LIMB SURGERIES UNDER SPINAL ANAESTHESIA

COMPARISON OF TWO DIFFERENT DOSES OF ORAL GABAPENTIN FOR POST OPERATIVE ANALGESIA IN LOWER LIMB SURGERY UNDER SPINAL ANAESTHESIA

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/01/017145

Enrollment

Registered

2019-01-17

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

None listed

Interventions

Intervention1: BUPIVACAINE (HEAVY): INTRATHECAL DOSE- 0.5% HEAVY 3.5 ML DRUG TO BE GIVEN INTRATHECALLY WITHOUT ADDITIVES Control Intervention1: GABAPENTIN: ORAL DOSE- 300 MG AND 600 MG DRUG TO BE GIVE

Eligibility

Inclusion criteria

Inclusion criteria: BOTH MALE AND FEMALE PATIENTS OF AGE GROUP 18-65 YRS RECEIVING SPINAL ANAESTHESIA FOR ELECTIVE LOWER LIMB SURGERIES UNDER ASA GRADE 1 AND 2

Exclusion criteria

Exclusion criteria: 1. PATIENTS WITH ALLERGY TO GABAPENTIN 2. PATIENTS SUFFERING FROM EPILEPSY, LIVER AND RENAL DISEASE, ANY CHRONIC PAIN SYNDROMES, PSYCHIATRIC ILLNESS 3. PATIENTS REQUIRING SURGICAL DURATION MORE THAN 3 HOURS

Design outcomes

Primary

Measure	Time frame
COMPARE TOTAL DURATION OF ANALGESIA AND TOTAL NUMBER OF ANALGESICS REQUIRED IN THE FIRST 24 HOURS AFTER SURGERYTimepoint: 24 HOURS	—

Secondary

Measure	Time frame
COMPARE SIDE EFFECTS OF THE TWO DOSES OF GABAPENTIN IF ANYTimepoint: 24 HOURS	—

Countries

India

Contacts

Public ContactMITALEE H PAREEK

MGM MEDICAL COLLEGE AND HOSPITAL

kppnayak@yahoo.com9422209729

Outcome results