Skip to content

Comparison of perioperative efficacy of analgesia and spinal position between the ultrasound guided PENG block and SIFI block in hip surgeries

Comparative efficacy of peri-operative analgesia and ease of spinal position between ultrasound guided Pericapsular Nerve Group (PENG) block and Supra Inguinal Fascia Iliaca (SIFI) block in hip surgeries â?? A double blinded randomized controlled trial.

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026448
Enrollment
90
Registered
2020-07-09
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: O- Medical and Surgical

Interventions

Intervention1: Comparison of analgesia between Ultrasound guided periencapsular nerve group block versus ultrasound guided suprainguinal fascia iliac block: Comparative efficacy of perioperative anal

Sponsors

S Nijalingappa Medical College and HSK Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Iâ??• patients Body mass index Patients undergoing elective hip surgeries like femur neck intertrochanteric and subtrochanteric fracture

Exclusion criteria

Exclusion criteria: Patient refusal to give consent. Infection at site of injection. Allergy to local anaesthetics. Patients receiving opioids for chronic analgesic therapy. Coagulopathy Patients with inguinal hernia on the same side of hip pathology

Design outcomes

Primary

MeasureTime frame
Assessment of perioperative analgesia by numerical rating scale (NRS) between two study groups at rest and straight leg raise of affected limb to 15 degrees Timepoint: NRS pain score 30 minutes before and after administration of block

Secondary

MeasureTime frame
Ease of spinal position between two groups by using ease of spinal position scale (EOSP). Comparison of amount of consumption of rescue analgesia between two groups. Observation of any complications during the study. Timepoint: Every 2 hourly after performing block

Countries

India

Contacts

Public ContactDr Naveen R

S Nijalingappa Medical College Navanagar Bagalkot 587102

basavarajapothnal@gmail.com9886334039

Outcome results

None listed

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