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Effect of Pregabalin(modified pain killer) on duration of pain relief after spinal anaesthesia in patients undergoing surgeries below umbilicus.

The effect of single dose of oral pregabalin on the duration of analgesia after spinal anaesthesia in patients undergoing elective infraumblical surgeries-A randomized control study in tertiary care teaching hospital - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056707
Enrollment
100
Registered
2023-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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: CAPSULE PREGABLIN 150MG: Single oral dose of Pregabalin 150 mg given one hour before spinal anesthesia for postoperative analgesia upto 8 hrs without any other analgesia Control Interve

Sponsors

Dr Naresha G N
Lead Sponsor
sims shimoga
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA I AND II patients Patients undergoing infraumblical surgeries under spinal anaesthesia

Exclusion criteria

Exclusion criteria: ASA III AND ASA IV patients Patient refusal Patients contraindicated for spinal anaesthesia Patients having chronic pain and neurological problems and patients who is on NSAIDS or other analgesics

Design outcomes

Primary

MeasureTime frame
Time to VAS more than 3 i.e time to rescue analgesics in minutes noted & patients will be given Inj. Diclofenac 1.0mg/kg intramuscular as rescue analgesic once VAS exceeds 3. Timepoint: analgesia should be more than 8 hours

Secondary

MeasureTime frame
ime to VAS more than 3 i.e time to rescue analgesics in minutes noted & patients will be given Inj. Diclofenac 1.0mg/kg intramuscular as rescue analgesic once VAS exceeds 3. Timepoint: within 8 hours

Countries

India

Contacts

Public ContactDr Naresha G N

SHIMOGA INSTITUTE OF MEDICAL SCIENCES SHIMOGA

ashwini.satrasala@gmail.com9980812398

Outcome results

None listed

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