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COMPARING OF TWO TYPES OF REGIONAL NERVE BLOCK IN PATIENTS POSTED FOR HIP SURGERIES ,PENG VERSUS FASCIA ILIACA BLOCK

â??COMPARISON OF PERI-CAPSULAR NERVE GROUP BLOCK VERSUS FASCIA ILIACA BLOCK IN HIP FRACTURE SURGERIES A RANDOMISED CONTROL STUDYâ??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033296
Enrollment
60
Registered
2021-04-30
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: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Control Intervention1: PENG Block VERSUS Fascia block: Patients will be randomly divided into 2 groups namely group PB and group FB in a sealed envelope. Group PB will receive Pericapsular nerve g

Sponsors

Dr Ashna Shetty
Lead Sponsor
Dr Madhumala
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged between 18 â?? 80 years undergoing elective cases of hip fracture surgeries like intertrochanteric, subtrochanteric , total hip replacement and hip arthroplasties. 2. Patients willing to give written informed consent[annexure 1(a)] 3. Patients belonging to ASA I and II[annexure 3(a)]

Exclusion criteria

Exclusion criteria: 1. Patients with coagulopathy 2. Patients with infection at the injection site 3. Patients with allergy to local anesthetics 4. Patients with severe cardiopulmonary disease (>=ASA IV) 5. Patients who are diabetic or other neuropathies 6. Patients receiving opioids for chronic analgesic therapy 7. Patients with contraindication to spinal anesthesia 8. Patients who are unable to comprehend visual analog scale (VAS)

Design outcomes

Primary

MeasureTime frame
Reduction in pain (VAS) score following the block Prolongation of sensory blockade Time for sensory regression Total duration of sensory blockade Total duration of analgesia will be noted Timepoint: 12 weeks

Secondary

MeasureTime frame
Post operative pain will be assessed using visual analogue scale (0-10) which will be followed by Pericapsular nerve group block or Fascia iliaca block and visual analogue score will be reassessed Visual analogue scores for pain recorded immediate post subarachnoid blockade, then 2nd hourly for first 6 hours, and at 12 and 24 hours post operatively. Analgesic requirement for first 24 hours post operatively. Adverse effects if any Timepoint: 12 weeks

Countries

India

Contacts

Public ContactDr Madhumala

Bangalore Medical College and Research Institute

drmadhumala@gmail.com9886786768

Outcome results

None listed

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