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Comparing pain experienced while sitting for spinal anesthesia and postoperative analgesia in suprainguinal and infrainguinal approaches for Fascia Iliaca Compartment block using an ultrasound machine in patients undergoing elective femoral fracture surgery.

Ultrasound guided Fascia Iliaca Compartment block comparing suprainguinal and infrainguinal approaches: A prospective randomized study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074031
Enrollment
100
Registered
2024-09-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: S729- Unspecified fracture of femur

Interventions

Intervention1: Suprainguinal Fascia Iliaca Compartment block: Suprainguinal Fascia Iliaca Compartment block with 30 ml of 0.2% Ropivacaine will be given under USG guidance. Control Intervention1: Infr

Sponsors

Dr Rishabh Srivastava
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age- 18 to 80 years of either gender. 2) Patients belonging to ASA Physical Status I and II. 3) Patients undergoing elective femoral fracture surgery.

Exclusion criteria

Exclusion criteria: 1) Patients refusal for the procedure. 2) Patients with history of allergy, sensitivity or any kind of reactions to local anaesthetic agents. 3) Patients with bleeding disorders or any significant coagulopathies and other contraindications for regional anesthesia. 4) Infection of the skin at the injection site. 5) Any lesion obscuring sonoanatomy. 6) Patients with pre-existing significant systemic diseases. 7) Patients on anticoagulants. 8) Patients with psychiatric illness. 9) Patients receiving combined spinal-epidural for lower limb surgeries 10) Inability to comprehend NRS scale.

Design outcomes

Primary

MeasureTime frame
1) Pain experienced while sitting for spinal anesthesia 2) Postoperative analgesiaTimepoint: Postoperative analgesia- Pain will be assessed using pain score: Numerical Rating Scale at 2nd, 4th, 6th, 8th, 10th, 12th, 14th, 16th, 18th, 20th, 22nd and 24th hour postoperatively.—

Secondary

MeasureTime frame
Anatomical visualization of structures (good/poor)Timepoint: This will be noted while giving block.;Area of drug spread achievedTimepoint: This will be assessed immediately after giving block.;Duration of sensory blockTimepoint: The sensory affect will be assessed immediately after giving block & noting the onset time, which is time for the end of the injection to dull response to pin prick, & noting the peak time, which is time for the end of the injection to no response to pin prick.;Duration taken to give blockTimepoint: This will be noted while giving block.;Time to rescue analgesiaTimepoint: This will be assessed in the postoperative period.;Visualization of needle (whole length/ partial length)Timepoint: This will be noted while giving block.—

Countries

India

Contacts

Public ContactVishwanath

Navodaya Medical College, Hospital And Research Centre

VISHWANATH.METI@GMAIL.COM9886777750

Outcome results

None listed

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