A clinical trial to study the effect of fascia iliaca compartment block versus combined pericapscular nerve group and lateral femoral cutaneous nerve block in patients for postoperative pain management in hip surgeries.

To compare the effectiveness of fascia iliaca compartment block versus combined pericapsular nerve group and lateral femoral cutaneous nerve block for postoperative analgesia in hip surgeries.

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/059842

Enrollment

Registered

2023-11-15

Start date

Unknown

Completion date

Unknown

Last updated

2023-12-19

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: Fascia iliaca compartment block(FICB) for postoperative analgesia in hip surgeries.: Patients belong to the group F(FICB) will be given ultrasound guided FICB with 25ml of 0.25% bupiva

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of above 18years. 2. Patients belonging to ASA grading I and II. 3. Patients undergoing only hip fracture (neck of femur fracture ,intertrochanteric fracture, subtrochanteric fracture)surgeries.

Exclusion criteria

Exclusion criteria: 1. Patients having contraindication for subarachnoid block. 2. Infection at the site of block. 3. Any history of allergic to study drugs. 4. Patients on term analgesic for chronic pain. 5. Patient with coagulopathy. 6. Conversion to general anesthesia during surgeries. 7. Patients having multiple trauma. 8. Pregnant patients.

Design outcomes

Primary

Measure	Time frame
1. The duration of postoperative analgesia in patients received Fascia iliaca compartment block(FICB). 2. The duration of postoperative analgesia in patients received combined pericapsular nerve group block (PENG) and lateral femoral cutaneous nerve block(LFCNB) 3. Postoperative Numerical Rating Score(NRS). 4. Postoperative analgesic requirement.Timepoint: 15 min from the time of administration. 15min from the time administration. 3hr,6hr,12hr,24hr,48hr in 48hrs	—

Measure

Time frame

1. The duration of postoperative analgesia in patients received Fascia iliaca compartment block(FICB). 2. The duration of postoperative analgesia in patients received combined pericapsular nerve group block (PENG) and lateral femoral cutaneous nerve block(LFCNB) 3. Postoperative Numerical Rating Score(NRS). 4. Postoperative analgesic requirement.Timepoint: 15 min from the time of administration. 15min from the time administration. 3hr,6hr,12hr,24hr,48hr in 48hrs

—

Secondary

Measure	Time frame
1. Ease of positioning (EOSP)for subarachnoid block was assessed on the scale of 0,1,2,3. 2. Patients satisfaction score 3. Degree of quadriceps weakness by muscle power score(MPS)Timepoint: After 15 minutes of nerve block After 48hours of nerve block After 48hours of nerve block	—

Countries

India

Contacts

Public ContactDr Smruthi C S

DM Wayanad Institute Of Medical Science,Wayanad

hod.anesthesiology@drmoopensmc.ac.in7406784848

Outcome results

None listed

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