Skip to content

Comparision of postoperative analgesia in patients undergoing hip surgeries with ultrasound guided fascia iliaca block using different local anaesthetics combination

To compare the efficacy of clonidine and dexmedetomidine as adjuvants to ropivacaine for postoperative analgesia in ultrasound guided suprainguinal fascia iliaca compartment block for patients undergoing elective hip surgeries. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066191
Enrollment
30
Registered
2024-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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 Clonidine 0.1mcg/kg: Injection Clonidine 0.1mcg/kg added to Injection Ropivacaine 0.2% 40 ml as single dose in interfascial plane. Control Intervention1: Injection Dexmedetomi

Sponsors

Chamarajanagar Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient accepting to participate with written informed consent. Patients belonging to ASA with physical status grade 1 and 2 of either sex. Patient with age group between 18 to 70 years posted for elective major hip surgeries.

Exclusion criteria

Exclusion criteria: Patient allergic to study drug or hypersensitivity to local anesthetics. Patient with cardiac disease, hepatic disease, renal disease, hypothyroidism, neuropathy, local site infection, bleeding diathesis, COPD, Obstructive sleep aponea . Patient on beta blockers, bradycardia (heart rate Patient with BMI >30 kg/m2.

Design outcomes

Primary

MeasureTime frame
Pain scores will be assessed as per visual analogue scale and the time needed for rescue analgesiaTimepoint: assessed over 24 hours every 5 minutes for first half an hour followed by every 2 hours for next 24 hours.

Secondary

MeasureTime frame
a) To study hemodynamic changes between two groups of patients. b) To assess the sedation among two groups of patients.Timepoint: 24 hours

Countries

India

Contacts

Public ContactDr Nandakishore B R

Chamarajanagar Institute of Medical Sciences

darshanms_jss@yahoo.com9741376797

Outcome results

None listed

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