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Compare intravenous paracetamol as pre-emptive vs preventive analgesic on post operative pain in open elective below umbilical surgeries under general anaesthesia in paediatric patients.

A prospective randomised study to compare intravenous paracetamol as preemptive vs preventive analgesic on postoperative pain in open elective below umbilical surgeries under general anaesthesia in paediatric patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079431
Enrollment
50
Registered
2025-01-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Q541- Hypospadias, penile

Interventions

Intervention1: Injection.Paracetamol: Group PE (Pre-emptive group) will be given 15 mg/kg of intravenous paracetamol in 20 mL of normal saline over 5mins
15mins before induction of GA. Control Intervention1: Injection.paracetamol: Group PV (Preventive group) will be given 15 mg/kg of intravenous paracetamol in 20 mL of normal saline after closure.

Sponsors

Jawaharlal nehru medical collage AMU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: weight more than 10kgs open abdominal surgeries operation time less than 120 minutes ASA 1 and ASA2

Exclusion criteria

Exclusion criteria: 1) Refusal of patients attendant/guardian 2) psychiatric illness. 3) H/O allergy /hypersensitivity to paracetamol, NSAIDS 4) Haemodynamically unstable patients. 5) Hepatic and renal dysfunctions 6) Use of anticoagulants.

Design outcomes

Primary

MeasureTime frame
Time to first rescue paracetamol after extubationTimepoint: 1 hr, 24 hr

Secondary

MeasureTime frame
1. Total paracetamol consumption in 24hours post surgery(mg) 2. Total number of patients requiring rescue paracetamol 3. Total number of patients requiring Break through analgesic (Ketorol) and Total Ketorol consumption(mg) 4. Pain score at 1hour in PACU and cumulative pain score at 24 hours 5. Side effects (vomiting, bleeding from site, stomach ache, hematemesis, allergy, anaphylactic reaction) 6. Parental satisfaction evaluated using a five-point Likert scale (very satisfied: 5, satisfied: 4, neutral: 3, dissatisfied: 2, and very dissatisfied: 1) Timepoint: 1hr, 24hr

Countries

India

Contacts

Public ContactMushahid Raza Khan

Jawaharlal nehru Medical College,Aliagrh Muslim University

drshahna.farhan@gmail.com9411979684

Outcome results

None listed

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