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A comparision between block characteristics of intrathecal hyperbaric bupivacaine and hyperbaric levobupivacaine in surgeries below umbilicus

A comparision between block characteristics of intrathecal hyperbaric bupivacaine versus hyperbaric levobupivacaine in patients undergoing infraumbilical surgeries a randomized clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090119
Enrollment
130
Registered
2025-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: - Health Condition 2: 4- Measurement and Monitoring

Interventions

Intervention1: Inj Bupivacaine heavy: Study participants will be randomized into two groups. One group will receive 3 ml Inj Bupivacaine heavy intrathecally before infraumbilical surgery starts and we

Sponsors

Dr Nabanita Debnath
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo elective infraumbilical surgeries under spinal anaesthesia with the following criteria will be enrolled: Age:18 to 60 years Gender: male and female gender, Details:American Society of Anaesthesiologist (ASA) physical status I & II.

Exclusion criteria

Exclusion criteria: Patients with the following criteria will be excluded-1.refuse to give consent 2.infection at the site 3.spinal deformity 3.history of allergy to study drugs 4.Patient on anticoagulant and antiplatelate 5.uncontrolled hypertension, diabetes mallitus,respiratory system disease,kidney disease 6.psychiatric patient 7.pregnant women 8.Patient undergoing emergency surgeries 9. weight less than 45 and more than 110 10.height less than 140cm and more than 180cm.

Design outcomes

Primary

MeasureTime frame
Motor and sensory block characteristicsTimepoint: We will record time of onset of motor block,duration and regression of motor block. For sensory block,we will record time of onset of sensory block and level of sensory block every 2 mins uptil 10 mins,every 5 minutes uptil 30 mins then every 10 minutes uptil closure of operative site as well as time of 2 segments regression of sensory block.

Secondary

MeasureTime frame
Heamodynamic changes & any adverse outcomeTimepoint: We will measure heart rate,systolic blood pressure, diastolic blood pressure & mean arterial pressure for heamodynamic changes every 2 mins for 1st 10 mins, every 5 mins for next 20 mins ,every 10 mins until the surgery gets over & nausea,vomiting as adverse effects intraoperatively.

Countries

India

Contacts

Public ContactDr Nabanita Debnath

Regional institute of medical science,Imphal

gojendrar68@gmail.com7005442623

Outcome results

None listed

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