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comparison of pain free period of two local anesthethic drug injections after hip surgery in patients using a special nerve block technique under ultrasound guidance.

Comparison of analgesic efficacy of 0.5 percent bupivacaine and 0.5 percent ropivacaine in pericapsular nerve group block for hip fracture surgeries under spinal anaesthesia a randomised single blinded study. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109285
Enrollment
60
Registered
2026-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: S721- Pertrochanteric fracture Health Condition 2: S720- Fracture of head and neck of femur

Interventions

Intervention1: Peng block with Bupivacine: Ultrasound guided Pericapsular nerve group block with adminstration of 0.5 percent Bupivacine with Dexamethasone 4mg injected in the Fascial plane between Ps

Sponsors

Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA Grade I to ASA III 2. Elective Hip fracture and Hip replacement surgeries 3. Age 30-95 years of either sex

Exclusion criteria

Exclusion criteria: 1. Age less than 30 years or more than 95 years 2. ASA Physical Status IV - VI 3. Patient s refusal. 4. Allergy to the drugs used in the study 5. Pre-existing neuromuscular disorder or spinal deformities 6. Coagulation defect 7. Local site infection 8. Severe hypovolemia 9. Bilateral lower limb procedures

Design outcomes

Primary

MeasureTime frame
1)To evaluate and compare the ease of positioning during administration of spinal anaesthesia. 2)To asses duration of post operative analgesia provided by each local anaesthetic drug. Timepoint: To observe perioperative pain scores using VAS score at 0 min,15 min,30mins 1,2,4,6,8,10,12,16,20 and 24 hours

Secondary

MeasureTime frame
1) To evaluate and compare the post operative pain using VAS SCORE 2) To compare the total opioid consumption in first 24 hours between the two groups. 3) To observe the incidence of adverse effects with each local anaesthetics. 4) To assess and compare the hemodynamic parameters. Timepoint: To observe vitals at intervals and side effects at 0 min,15 min,30mins 1,2,4,6,8,10,12,16,20 and 24 hours

Countries

India

Contacts

Public ContactDr Kanta Bhati

Sardar Patel Medical College, Bikaner, Rajasthan

shakuntlajaisalmer95@gmail.com8824989901

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026