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A study to compare the effects of two approches of giving ultrasound guided fascia iliaca compartment block, using ropivacaine as local anaesthetic drug in patients undergoing surgery for various types of hip fractures.

A comparative study of post operative analgesic efficacy of suprainguinal versus infrainguinal approach of usg guided fascia iliaca compartment block using 0.2% ropivacaine in patients undergoing surgery for hip fracture under spinal anesthesia.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042774
Enrollment
50
Registered
2022-05-24
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur Health Condition 2: S721- Pertrochanteric fracture Health Condition 3: S722- Subtrochanteric fracture of femur

Interventions

Intervention1: Suprainguinal approach of usg guided fascia iliaca compartment block: With the patient supine, a linear high frequency probe (6-14 MHz) is placed in the sagittal plane to obtain an imag

Sponsors

Jawaharlal Nehru medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients belonging to ASA (American Society of Anaesthesiologists) class-I, II and III. 2) Patients undergoing hip surgeries of duration 1-3 hours with haemoglobin at least 9 gm/dl and platelet count more than 1lac.

Exclusion criteria

Exclusion criteria: 1)Patients not willing 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 ropivacaine or any other local anesthetic. 5)Local pathology at the site of injection or disability limiting the performance of block. 6)Pregnant, lactating mothers. 7)Inadequate block necessitating institution of general anaesthesia for continuation of surgical procedure.

Design outcomes

Primary

MeasureTime frame
Comparison of post operative assessment of effective analgesia in both the groups with the help of numeric rating scale NRS score in the first 24 hours.Timepoint: Around 1 year—

Secondary

MeasureTime frame
To assess sensory and motor block. To assess quality of recovery. To assess patients having any adverse effects or complications.Timepoint: Around 1 year—

Countries

India

Contacts

Public ContactDr Pooja Mathur

Jawaharlal Nehru medical college and hospital

drpoojarawat@gmail.com9414003933

Outcome results

None listed

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