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To Compare Effectiveness Of Periarticular Fentanyl and Ketorolac Injection for Pain Management in Total Hip Arthroplasty.

To Compare Effectiveness Of Periarticular Fentanyl and Ketorolac Injection for Pain Management in Total Hip Arthroplasty - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083311
Enrollment
90
Registered
2025-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: M15-M19- Osteoarthritis

Interventions

Intervention1: GROUP A - Bupivacaine and Fentanyl and Normal Saline: After getting approval from CRC and IEC.Patients undergoing Total Hip Arthroplasty . Inclusion and exclusion criteria will be appli

Sponsors

TEERTHANKAR MAHAVEER MEDICAL COLLEGE AND RESEARCH CENTRE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Non traumatic/elective cases of Primary Osteoarthritis, Secondary Osteoarthritis of hip due to Septic Arthritis, Tuberculosis and Avascular Necrosis. 2.Post traumatic Arthritis 3.Patient able to give informed consent and agrees to comply with the postoperative review programme.

Exclusion criteria

Exclusion criteria: 1.Patient undergoing revision surgery or second stage THA. 2.Patient with fresh trauma. 3.Patient having associated complain of low backache. 4.Patient is immobile or has another neurological condition affecting musculoskeletal function 5.Patient with major psychological problems or neurological deficit. 6.Patient with previous drug dependence, tolerance to any of the ingredient of the injection or allergy to any of the ingredients of the injection. 7.Patient with hepatic,Renal insufficiency.

Design outcomes

Primary

MeasureTime frame
1.To Compare the efficacy of 2 types of periarticular cocktail injection in reducing post operative pain after total hip arthroplasty in comparison with normal saline. 2.To assess pain relief after Total Hip Arthroplasty in recruited patients. 3.To calculate cumulative dose of analgesic required after surgery. Timepoint: 6hr , 12hr, 24hr, 48hr

Secondary

MeasureTime frame
1.To calculate number of days after which patient become ambulatory 2.To calculate Length of hospital stay in days. Timepoint: 0 day , 14 day

Countries

India

Contacts

Public ContactDR AMIT SARAF
amitsaraf_75@yahoo.com9780029750

Outcome results

None listed

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