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Study comparing effect of dexmedetomidine with levobupivacaine in fascia iliaca compartment block in hip surgery patients for preoperqtive positioning and post operative pain

A comparative study of fascia ilaca compartment block With levobupivacaine and levobupivacaine with dexmedetomidine to alleviate the preoperative pain during positioning and postoperative analgesia in hip fracture under subararachnoid block.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043947
Enrollment
62
Registered
2022-07-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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: Fascia iliaca compartment block in patients with hip fracture: Comaparsion of drug levobupivacaine alone or levobupivacaine with dexmedetomidine in fascia iliaca compartment block give

Sponsors

Dr S N Medical College Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients aged 18 to 70 years of either gender of ASA physical statue I or II undergoing hip fracture surgery who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Patient refusal 2.Hypersensitivity to amide local anaesthetics 3.Infection at the injection site 4.Pregnant woman 5.Obesity (BMI is 30 or higher) 6.Uncooperative patients 7.Anatomical abnormality (Pathological fracture ,previous surgery at same site) 8.Bleeding disorders (INR more than 1.5) 9.Peripheral neuropathy 10.Cognitive impairment (Abbreviated Mental Test Score less than 6 points) 11.Concurrent chronic analgesic therapy (NSAIDS,Tramadol), 12.Known hepatic or renal insufficiency

Design outcomes

Primary

MeasureTime frame
To study and compare FICB with levobupivacaine And levobupivacaine with dexmedetomidine in hip fracture under spinal anesthesia with regard to positioning of patient during spinal anesthesia in terms of Visual Analog Scale (VAS) score.Timepoint: 30 minutes—

Secondary

MeasureTime frame
To compare the following in both groups during preoperative and perioperative period -Duration of postoperative analgesia in terms of VAS score,Hemodynamic parameters (Heart Rate,MBP,SBP,DBP,SPO2),To assess any side effects such as hypotension, bradycardia, and sedation associated with the drug,Patient Satisfaction Score at the end of the study.Timepoint: 24 hours—

Countries

India

Contacts

Public ContactShobha Ujwal

Dr S N Medical College

drshobhaujwal@gmail.com9461028789

Outcome results

None listed

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