Skip to content

Feasibility of single puncture PENG-SIFI Block for postoperative analgesia in patients undergoing hip surgery

The distance between the femoral condyle and the popliteal artery: Does it affect needle placement in ipACK brock at the level of femoral condyles? An observational study. - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061236
Enrollment
30
Registered
2024-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: M97- Periprosthetic fracture around internal prosthetic joint

Interventions

Intervention1: Single Puncture PENG-SIFI: PENG-SIFI block will be given under USG guidance once before the surgery Control Intervention1: NIL: NIL

Sponsors

Sancheti Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients presenting for proximal femur fracture surgery (intertrochanteric, neck of femur and subtrochanteric fractures) and consenting for the trial will be included.

Exclusion criteria

Exclusion criteria: inability or refusal to sign informed consent, younger than 50 years, BMI greater than 35 kg/m2, intolerance to any of the drugs used in the study, a history of hepatic or renal insufficiency, coagulopathy, using chronic analgesic drugs; having additional illnesses, including liver or kidney diseases, neurological deficits in the lower extremities and illnesses that interfered with communication skills such as dementia or mechanical ventilation requirement

Design outcomes

Primary

MeasureTime frame
Total TramadolTimepoint: Total Tramadol consumption in first 24 hours after surgery

Secondary

MeasureTime frame
NRS scores during resting and movementTimepoint: at 0, 2, 4, 12 and 24 hrs postop;Opioid-related complications and motor weakness after blockTimepoint: 0, 2, 4, 12 and 24 hrs postop;Patient satisfaction (NRS score 0-10; 0-very unsatisfied and 10-very satisfied)Timepoint: 24 hours after surgery;Time to first analgesic requestTimepoint: 0, 2, 4, 12 and 24 hrs postop

Countries

India

Contacts

Public ContactSandeep Diwan

Sancheti Hospital

sdiwan14@gmail.com9823029328

Outcome results

None listed

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