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To assess analgesic efficacy of Dexmedetomidine as an adjuvant to bupivacaine in Ultrasound Guided Femoral Nerve Block in Patients Undergoing Elective Surgery for Fracture Shaft of Femur in department of Anaesthesia, SMS Medical college Jaipur

Randomized control study to assess the analgesic efficacy of Dexmedetomidine as an Adjuvant to Bupivacaine in Ultrasound Guided Femoral Nerve Block in Patients Undergoing Elective Surgery for Fracture Shaft of Femur in department of Anaesthesia, SMS Medical college Jaipur - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058940
Enrollment
90
Registered
2023-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system Health Condition 2: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: 15ml of 0.25% bupivacaine and 1 ug /kg of dexmedetomidine in 2ml of NS in 45 patients: patient will receive ultrasound guided femoral nerve block by using 15ml of 0.25% bupivacaine an

Sponsors

Sawai man singh medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient undergoing elective surgery for fracture shaft of femur. Patients consenting to participate. Adult patients aged 20-70 Years. Patients belonging to American Society of Anesthesiologists (ASA) grade I, II and III

Exclusion criteria

Exclusion criteria: Patients with psychiatric illness, anxious, agitated. Patients with peripheral sensorineural deficit. Patients allergic to local anesthetics. Patients with contraindications to regional anaesthesia. Patients with suspected compartment syndrome in lower limbs. Patients on analgesia within 8 hours before performing nerve block. Block failure cases(If NRS score is not

Design outcomes

Primary

MeasureTime frame
1.To assess & compare the difference in mean time of first rescue analgesia in both groups by using NRS score. 2.To observe change in NRS at one minute interval maximum up to 20 minutes after administration of block until NRS 3 for positioning of patient for spinal anaesthesia in both groups 3.To determine the difference in mean dose of analgesic required for 24 hours in both groups. Timepoint: 24 hours post operatively—

Secondary

MeasureTime frame
1.To assess quadriceps muscle strength using Oxford muscle strength grading. 2.To determine the change in the hemodynamic parameters (HR,SBP,DBP,MAP & SpO2) in both groups. 3.To observe side effect or complication, if any. Timepoint: 24 hours post operatively—

Countries

India

Contacts

Public ContactDr Pooja

SMS MEDICAL COLLEGE

drmamtakhandelwal@gmail.com9929338174

Outcome results

None listed

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