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Effect of combination of drugs on pain relief in patients undergoing surgery for fracture of lower limb

Efficacy of preemptive multimodal analgesia for post operative pain relief in trauma patients undergoing lower limb surgery-A Randomised trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/02/006692
Enrollment
250
Registered
2016-02-29
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- ASA status I to II patients undergoing post traumatic long bone surgeries of femur and tibia

Interventions

Intervention1: Group PE: This group will receive preemptive multimodal pharmacologic agents
Intravenous diclofenac 75 mg, intravenous morphine 3mg, 1gm of intravenous acetaminophen and 75mg pregabalin per orally one hour before the start of surgery Control Intervention1: Group C: Will not re

Sponsors

Post Graduate Institute Of Medical Education Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing post traumatic long bone surgeries of femur and tibia.

Exclusion criteria

Exclusion criteria: History of associated head injury, blunt trauma abdomen or blunt trauma chest 2) allergy and contraindications to any of the medications being used 3) history of being on chronic pain medications (i.e. slow-release preparations of opioids) 4) rheumatoid arthritis 4)psychiatric disorder 5) a history of diabetes with impaired renal function 6) morbid obese 7) patients unable or unwilling to use patient-controlled epidural analgesia (PCEA). (8) prior use of the investigated medications (9) current use of anticoagulants or antiplatelet medication

Design outcomes

Primary

MeasureTime frame
Mean number of boluses of PCA or PCEATimepoint: At 24 and 48 hrs

Secondary

MeasureTime frame
Mean VAS scores in post operative period Postoperative nausea, vomiting, sedation scoresTimepoint: 30 min, 1 hr, 2 hrs, 4hrs, 8hrs, 12 and 24 hrs and on postoperative day 2.

Countries

India

Contacts

Public ContactJeetinder kaur

POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH

jeet1516@gmail.com7087009510

Outcome results

None listed

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