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To compare effect of two different local anaesthetic drugs given through spinal anaesthesia

TO COMPARE BLOCK CHARACTERISTICS OF INTRATHECAL HYPERBARIC LEVOBUPIVACAINE WITH FENTANYL VERSUS INTRATHECAL HYPERBARIC BUPIVACAINE WITH FENTANYL IN UROLOGICAL SURGERIES: A Randomized Double-Blind Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/048724
Enrollment
176
Registered
2023-01-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: N398- Other specified disorders of urinary system

Interventions

Intervention1: Hyperbaric Levobupivacaine and fentanyl: Hyperbaric levobupivacaine at 12.5mg with fentanyl at25mcg with spinal needle in subarachnoid space after regular backflow of csf Control Interv

Sponsors

Vikash Kumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA physical status 1, 2 Patients able to comprehend and willing to participate. Patients scheduled for general elective surgeries

Exclusion criteria

Exclusion criteria: Patients who refuse to participate Patients allergic to levobupivacaine and/or bupivacaine Patients having infection at drug administration site Patient having coagulopathy Patient having pre existing neurological condition Raised intracranial pressure Any other absolute contraindication to spinal anaesthesia Uncooperative patients Body weight above 100 kg

Design outcomes

Primary

MeasureTime frame
To compare the block characteristics in regard of onset and duration of sensory and motor blockade between two group Timepoint: Upto 3hours

Secondary

MeasureTime frame
To compare the hemodynamic parameters and adverse effects between themTimepoint: 24hours postoperative

Countries

India

Contacts

Public ContactDr Mumtaz Hussain

Indira Gandhi Institute Of Medical Sciences

drhussain72@yahoo.co.in9473376853

Outcome results

None listed

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