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Multiple modalities for pain management in post surgery patients at an Orthopaedic surgery centre.

Multimodal analgesia in post operative patients at a tertiary care Orthopaedic centre - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069007
Enrollment
190
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Injection Paracetamol and Injection Tramadol: Patients in post operative period will be administered weight adjusted dosage of Injection Paracetamol intravenously every 8 hours and weig

Sponsors

Base Hospital Delhi Cantt
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients undergoing surgical intervention for complex fractures at Dept of Orthopaedics, Base Hospital Delhi Cantt. 2. All patients undergoing arthroscopy and arthroplasty at Dept of Orthopaedics, Base Hospital Delhi Cantt. 3. Age group: All adult patients in the age group between 20 to 80 years. 4. Both male and female

Exclusion criteria

Exclusion criteria: 1. Patients with a history of adverse drug reaction to Acetaminophen/paracetamol, Gabapentinoids, Opioids and their derivatives. 2. Patients on Immuno-modulator therapies. Patients with multi-system injuries involving Head injury, Abdominal trauma, Thoracic and Spine injuries and multiple fractures. 3. Patients with deranged Liver and Renal Function during pre-op evaluation. 4. Paediatric cases 5. Patients unwilling to give consent to be a part of the study.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of analgesia of Injection Paracetamol with Injection Tramadol (Group A) and Injection Paracetamol with Oral Gabapentin (Group B) using Visual Analogue Score.Timepoint: Immediate (0 hour), 12, 24, 48 and 72 Hours post operative period.

Secondary

MeasureTime frame
To compare the pace of post operative rehabilitation between Group A and Group B using range of motion and ambulatory status.Timepoint: Immediate (0 hour), 12, 24, 48 and 72 Hours post operative period.

Countries

India

Contacts

Public ContactDhairya Khera

Base Hospital Delhi Cantt

dhairyakhera90@gmail.com9005890477

Outcome results

None listed

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