FindTrial
Sign In

A clinical trial to study the efficacy of different volumes of 0.2% ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgery

Efficacy of different volumes of 0.2% ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036144
Enrollment
90
Registered
2021-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: Ultrasound guided Suprainguinal Fascia Iliaca Compartment Block: Patients will receive suprainguinal fascia iliac compartment block with 40 ml of 0.2% Ropivacaine Control Intervention1:

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Patients scheduled for lower limb surgeries, including the hip and uptown the knee joint -ASA I,II and III patients -Cognitive ability to comprehend NRS scale

Exclusion criteria

Exclusion criteria: -Patient refusal -Contraindications to the suprainguinal fascia iliaca compartment block (such as coagulopathies, infection at injection site, allergy to local anaesthetic) -Patient on chronic opiod abuse -Neuropathies

Design outcomes

Primary

MeasureTime frame
To comparatively evaluate the efficacy of different volumes of ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgeries -Time to first request of rescue analgesia with in first 24 hours after surgery -Total requirement of analgesics for pain management in first 24 hoursTimepoint: To comparatively evaluate the efficacy of different volumes of ropivacaine in suprainguinal fascia iliaca compartment block for multimodal analgesia in lower limb surgeries -Time to first request of rescue analgesia with in first 24 hours after surgery -Total requirement of analgesics for pain management in first 24 hours—

Secondary

MeasureTime frame
Patient satisfaction with pain managementTimepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Jessica Sekhon

Dayanand Medical College and Hospital, Ludhiana

jessicasekhon94@yahoo.com9464532923

Outcome results

None listed

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