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A comparative study of two anaesthetic combinations for infraumbilical surgeries.

A Prospective Randomised Double Blind Comparative Study Of Intrathecal Levobupivacaine (0.5%) With Dexmedetomidine (5micrograms) Versus Intrathecal Bupivacaine (0.5%) With Dexmedetomidine (5micrograms) For Infraumbilical Surgeries. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060257
Enrollment
50
Registered
2023-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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: Intrathecal Bupivacaine (0.5%) and Dexmedetomidine (5 micrograms): Single dose of 3.4 ml of 0.5% Bupivacaine + 5 micrograms of Dexmedetomidine given intrathecally. Control Intervention1

Sponsors

Dr Bharggavi Venkat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective infraumbilical surgeries willing to give written informed consent. 2. ASA physical status I and II

Exclusion criteria

Exclusion criteria: 1. Contraindications to spinal anaesthesia 2. Allergy to study drugs 3. Patients with history of drug abuse and psychiatric disease 4. Morbidly obese patients of BMI >35kg/m2

Design outcomes

Primary

MeasureTime frame
Onset and Duration of sensory and motor blockTimepoint: Assessed at 0,2,4,6,8,10 mins

Secondary

MeasureTime frame
Hemodynamic ParametersTimepoint: Assessed at 15 mins,30 mins,45 mins,60 mins,75 mins,90 mins;Perioperaative Analgesia and SedationTimepoint: Assessed at 2hrs,4hrs,6,hrs,8hrs,10hrs,12hrs,14hrs,16hrs,18hrs,20hrs,22hrs,24hrs;Postoperative duration of sensory and motor blockTimepoint: Assessed at 15 mins,30 mins,45 mins,60 mins,75 mins,90 mins

Countries

India

Contacts

Public ContactDr Geetanjali M

BGS Global Institute of Medical Sciences

bharggavivenkat@gmail.com9901209981

Outcome results

None listed

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