EVALUATION OF POST OPERATIVE PAIN AFTER GIVING PRE-EMPTIVE ANALGESIA WITH PARACETAMOL IN OPEN INGUINAL HERNIA MESH REPAIR.

Evaluation of post-operative pain following preemptive analgesia with intravenous Paracetamol in Unilateral Lichtensteins Inguinal Hernia Repair surgery, Randomised Control Trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065619

Enrollment

Registered

2024-04-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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: iv paracetamol 15mg/kg body weight: Dose- 15mg/kg body weight in 100ml Normal Saline Frequency- once Route of administration- Intravenous Duration- 30min Control Intervention1: NORMAL S

Eligibility

Inclusion criteria

Inclusion criteria: age 18 and above unilateral Lichtenstein inguinal hernia mesh repair under spinal anaesthesia a?a grade 1 and 2 informed consent

Exclusion criteria

Exclusion criteria: hypersensitivity to paracetamol different procedure for inguinal hernia epidural anaesthesia

Design outcomes

Primary

Measure	Time frame
VAS pain score decreases significantly Need for rescue analgesia reducedTimepoint: 6hrs, 12hrs, 24hrs, 36hrs, 48hrs, 72hrs	—

Secondary

Measure	Time frame
REDUCTION IN USE OF RESCUE ANALGESIA LIKE DICLOFENAC OR TRAMADOLTimepoint: 6hrs, 12hrs, 24hrs, 36hrs, 48hrs,72hrs	—

Countries

India

Contacts

Public ContactDr V M Uppin

drvmuppin@hotmail.com9845273505

Outcome results

None listed

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