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comparison of efficacy of two drugs that is high pressure ropivacaine 0.75% and high pressure levobupivacaine 0.5% in below the umbilical surgeries.

Efficacy of intrathecal block with hyperbaric ropivacaine 0.75% and hyperbaric levobupivacaine 0.5% in infraumbilical surgeries: a randomised control study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057945
Enrollment
100
Registered
2023-09-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Control Intervention1: HYPERBARIC LEVOBUPIVACAINE 0.5%: Bupivacaine, an amino-amide compound, proved to be a very effective long-acting local anesthetic agent. The past millennium has exclusively been

Sponsors

DEPARTMENT OF ANESTHESIA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient with Age of 18–60 years 2.Patient of American Society of Anesthesiologists (ASA) physical status class I and II

Exclusion criteria

Exclusion criteria: 1.Patient’s refusal . 2.Patient having Bleeding disorders . 3.Patient having Neurological disease. 4.Patient having Local skin infections at the site of spinal block. 5.Patient having Severe back deformities . 6.Patient having Raised intracranial pressure . 7.Patient having Cardiac and respiratory disease . 8.Patient of Morbid obesity

Design outcomes

Primary

MeasureTime frame
1.Onset of sensory block: will be tested at every 2 min. intervals till the establishment of the block and every 5 min. during surgery. 2.Duration of sensory block: after completion of surgery the sensory block will be tested at 15 min. interval till its complete regression. 3.Onset of motor block: will be tested every 2 min. till establishment of block. 4.Duration of motor block: will be tested every 15 min. interval till its complete regression.Timepoint: 1.Onset of sensory block: will be checked at every 2 min. intervals till the establishment of the block and every 5 min. during surgery. 2.Duration of sensory block: after completion of surgery the sensory block will be tested at 15 min. interval till its complete regression. 3.Onset of motor block: will be tested every 2 min. till establishment of block. 4.Duration of motor block: will be tested every 15 min. interval till its complete regression.—

Secondary

MeasureTime frame
1.To compare the incidence of hemodynamic changes in terms of hypotension & bradycardia every 2,5,10,15,20,25 & 30 min. & thereafter every 10 min. interval till completion of surgery. 2.To compare incidence of complications for first 24 hours. Timepoint: 1.To compare the incidence of hemodynamic changes in terms of hypotension & bradycardia every 2,5,10,15,20,25 & 30 min. & thereafter every 10 min. interval till completion of surgery. 2.To compare incidence of complications for first 24 hours.—

Countries

India

Contacts

Public ContactDR SIMINPREET KAUR

MAHARAJA AGRASEN MEDICAL COLLEGE

dr.jyotiumesh@gmail.com8607672844

Outcome results

None listed

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