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Comparison of the duration of sensory anaesthesia in patients undergoing lower limb orthopaedic surgery under spinal anaesthesia with & without intravenous dexmedetomidine.

Comparison of the duration of sensory blockade of spinal anaesthesia with & without intravenous dexmedetomidine in patients undergoing lower limb orthopaedic surgery. - NILL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054571
Enrollment
58
Registered
2023-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: Intravenous Dexmedetomidine: Intravenous dexmedetomidine given as a bolus before spinal anaesthesia and as an infusion throughout the duration of surgery under spinal anaesthesia Contro

Sponsors

Maulana Azad Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult patients between the age of 18-65 years scheduled to undergo elective lower limb orthopaedic surgery under spinal anaesthesia. 2.Patients belonging to American Society of Anaesthesiologists(ASA) physical status I or II. 3.Patients in whom anticipated duration of surgery 4.Patient height between 150-175cms.

Exclusion criteria

Exclusion criteria: 1.Patients having skin infection at the site of subarachnoid block. 2.Patients with thrombocytopenia/bleeding disorders/coagulopathy. 3.Patients with h/o hypersensitivity to study drug. 4.Patients having a neuromuscular/neurological disease. 5.Patients having spinal deformity. 6.Patients with cerebral palsy and mental retardation. 7.Patients who are using any opioid/sedative medication. 8.Patients with a h/o alcohol or drug abuse. 9.Patients having a BMI >30kg/m2.

Design outcomes

Primary

MeasureTime frame
Duration of sensory block(minutes)Timepoint: Sensory block level will be assessed every 2 minutes for the initial 10 minutes of the surgery, and then every 5 minutes till the completion of the first hour of the surgery. Then after this, it will be assessed every 10 minutes for the rest of the duration of surgery.

Secondary

MeasureTime frame
Analgesic consumption over first 24 hours postoperativelyTimepoint: Total analgesic consumption of the patient in the first 24 hours post operatively will be noted.;Maximum level of sensory block achieved by spinal anaesthesiaTimepoint: Sensory block will be assessed every 2 minutes till maximum height of sensory block is attained.;Onset time & duration of motor blockade(minutes)Timepoint: Onset time of motor block is defined as the time interval(in minutes) between the intrathecal administration & attainment of Bromage score of 3. Duration of motor block is defined as the time interval(in minutes) from intrathecal administration to the point at which Bromage score is back to zero.;Onset time of sensory block(minutes)Timepoint: It is defined as the time interval(in minutes) between intrathecal administration & maximal spread of sensory block.;Post operative pain scoresTimepoint: It will be assessed post operatively just on arrival of the patient in the post anaesthesia care unit & at 4 hours, 8 hours, 12 hours and 24 hours post operatively.;Time to requirement of first analgesicTimepoint: The time interval post operatively at which the pain score(VAS score) of patient is more than or equal to 3.

Countries

India

Contacts

Public ContactSimran Chahal

Maulana Azad Medical College

drakgk@yahoo.co.in9968604219

Outcome results

None listed

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