To determine the volume of drug required in fascia iliaca compartment block for pain relief in population of Assam

A study to evaluate 95% effective volume of 0.2% ropivacaine for ultrasound guided suprainguinal fascia iliaca compartment block-a single centre observational study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065422

Enrollment

Registered

2024-04-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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: Injection ropivacaine: 0.2% ropivacaine to be adminstered via USG guided to fascia iliaca compartment for analgesia Control Intervention1: Nil: Nil

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18 years to 45 years 2.Patients with BMI 18.5 to 24.9 kg/square meter 3.ASA status 1 and 2 4.Patients posted for elective orthopedic femur fractures and hip surgeries 5.Patient giving informed consent to participate in the study

Exclusion criteria

Exclusion criteria: 1.Patient unable to co-operate 2.Absolute contraindications for use of local anaesthetic agents or use of regional anaesthesia technique 3.Block failure or partial blocks 4.Pregnant and lactating patients 5.Patient with psychiatric diseases 6.Patient using psychoactive substances 7.Patient with impaired hearing 8.Patient using drugs for chronic pain

Design outcomes

Primary

Measure	Time frame
To evaluate 95% effective volume of 0.2% Ropivacaine for ultrasound guided suprainguinal fascia iliaca compartment block.Timepoint: To evaluate 95% effective volume of 0.2% Ropivacaine for ultrasound guided suprainguinal fascia iliaca compartment block in Orthopedic patients within 30 minutes of performing the blocks prior to surgery at baseline.	—

Secondary

Measure	Time frame
1.To determine the onset time of sensory block 2.To determine the hemodynamic changes following block 3.To determine the incidence of vessel puncture,haematoma or other intraprocedural complications.Timepoint: To determine the onset time of sensory block,hemodynamic changes following block,and any intraprocedural complications in Orthopedic patients within 30 minutes of performing the block prior to surgery at baseline.	—

Measure

Time frame

1.To determine the onset time of sensory block 2.To determine the hemodynamic changes following block 3.To determine the incidence of vessel puncture,haematoma or other intraprocedural complications.Timepoint: To determine the onset time of sensory block,hemodynamic changes following block,and any intraprocedural complications in Orthopedic patients within 30 minutes of performing the block prior to surgery at baseline.

—

Countries

India

Contacts

Public ContactDr Priyam Saikia

Gauhati Medical College and Hospital

saikia.priyam80@gmail.com9706067392

Outcome results

None listed

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