A comparative study evaluating the postoperative analgesic efficacy of suprainguinal versus infrainguinal approaches of ultrasound-guided fascia iliaca compartment block as single shot block using 0.25%,30ml ropivacaine in patients undergoing surgery for hip fracture under spinal anesthesia.

A comparison of analgesic efficacy of intravenous versus perineural dexamethasone with 0.25% bupivacaine in ultrasound guided infrainguinal fascia iliaca compartment block in patients undergoing lower limb surgery under spinal anaesthesia. - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/063235

Enrollment

Registered

2024-02-28

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

Health Condition 1: M966- Fracture of bone following insertion of orthopedic implant, joint prosthesis, or bone plate Health Condition 2: M966- Fracture of bone following insertion of orthopedic implant, joint prosthesis, or bone plate Health Condition 3: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified Health Condition 4: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal sys

Interventions

Intervention1: A COMPARISON OF ANALGESIC EFFICACY OF INTRAVENOUS VERSUS PERINEURAL DEXAMETHASONE WITH 0.25% BUPIVACAINE IN ULTRASOUND GUIDED INFRAINGUINAL FASCIA ILIACA COMPARTMENT BLOCK IN PATIENTS U

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group 18years and above. 2. Patients belonging to ASA (American Society of Anaesthesiologists) class-I, II and III

Exclusion criteria

Exclusion criteria: 1. Patients not giving consent to participate in the study. 2. Uncooperative patients. 3. Patient with chronic pain or on long-term analgesics. 4. Any known hypersensitivity or contraindication to bupivacaine or any other local anesthetic. 5. Local pathology at the site of injection or disability limiting the performance of block. 6. Inadequate block necessitating institution of general anaesthesia for continuation of surgical procedure

Design outcomes

Primary

Measure	Time frame
To assess the efficacy of perineural versus intravenous dexamethasone in prolonging analgesic duration of fascia illiaca compartment block for lower limb orthopedic surgeries.Timepoint: Within 24hours after completion of Surgery	—

Secondary

Measure	Time frame
1. To assess the duration of sensory block. 2. To assess the duration of motor block. 3. To assess & compare hemodynamic changes if any. 4. Total rescue analgesia consumption in 24 hrs. Timepoint: Within 24hours after completion of surgery	—

Countries

India

Contacts

Public ContactDr Vikram Singh Devanda

JLN medical college ajmer

drpoojarawat@gmail.com9414003933

Outcome results

None listed

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