A trial to understand the analgesics efficacy by different approach in a patient with hip bone fracture

A Randomized double-blind study to compare the analgesic efficacy of Ultrasound guided supra-inguinal versus conventional infra-inguinal approach for fascia iliaca compartment block in patient with hip bone fracture - Not applicable

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/090748

Enrollment

Registered

2025-07-11

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Health Condition 1: S741- Injury of femoral nerve at hip andthigh level

Interventions

Intervention1: Comparing the analgesic efficacy of 0.25% Bupivacaine by route of administration through different approaches in patients with unilateral hip bone fracture.: All the patients will under

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient willingness to participate in the study. 2. Patient between 18 to 75 years of age. 3. A radiographically confirmed unilateral hip bone fracture with NRS score more than 8. 4. BMI between 18-30 kilogram per meter square 5. ASA Grade I and II.

Exclusion criteria

Exclusion criteria: 1) Having suffered from major trauma or fracture of other bone 2)Refusal to participate. 3)Manifesting coagulopathy or deranged INR. 4)Currently on chronic analgesics, 5)A history of allergy to local anesthetics, 6)An infection in the area where FICB was to be performed, 7)Having significant visual, hearing or cognitive impairment 8)History of alcohol or drug abuse 9)Neuro-vascular disorder in the affected leg

Design outcomes

Primary

Measure	Time frame
To compare the duration of pain relief between supra-inguinal fascia iliaca compartment block (SIFIB) versus infra-inguinal fascia iliaca compartment block (IIFIB) in patient with unilateral hip bone fracture in terms of first dose of rescue analgesic.Timepoint: The intensity of pain will be recorded in both groups at the following time points: before the procedure (T0) and at 1hr (T1), 3hr (T2), 12hr (T3), and 24 hr (T4) after the procedure	—

Measure

Time frame

To compare the duration of pain relief between supra-inguinal fascia iliaca compartment block (SIFIB) versus infra-inguinal fascia iliaca compartment block (IIFIB) in patient with unilateral hip bone fracture in terms of first dose of rescue analgesic.Timepoint: The intensity of pain will be recorded in both groups at the following time points: before the procedure (T0) and at 1hr (T1), 3hr (T2), 12hr (T3), and 24 hr (T4) after the procedure

—

Secondary

Measure	Time frame
To compare the degree of pain relief in terms of Numerical Rating Scale(NRS). To record analgesic consumption during first 24 hours. To report any complication or side effects.Timepoint: The intensity of pain will be recorded in both groups at the following time points: before the procedure (T0) and at 1hr (T1), 3hr (T2), 12hr (T3), and 24 hr (T4) after the procedure	—

Countries

India

Contacts

Public ContactDr Hammad Usmani

Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh

hammadusmani2002@gmail.com9897114190

Outcome results

None listed

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