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Comparative study of intrathecal Levobupivacaine vs Bupivacaine vs Ropivacaine in perianal surgeries

A Comparative study of 0.5 percentage hyperbaric Levobupivacaine, 0.5 percentage hyperbaric bupivacaine and 0.75 percentage hyperbaric ropivacaine for subarachnoid block in perianal surgeries : A randomized control trial - Nil

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074982
Enrollment
69
Registered
2024-10-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Bupivacaine: Subarachnoid block using 2.5ml of 0.5 % Hyperbaric Bupivacaine in perianal surgeries. Time taken for the intervention is 5 to 20 minutes. Control Intervention1: Ropivacaine

Sponsors

Linda Monica Dsouza
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists (ASA) physical status Grade 1 and Grade 2 patients scheduled for elective or emergency perianal surgery requiring subarachnoid block

Exclusion criteria

Exclusion criteria: 1.Patients with spine deformity 2.Pregnant patients 3.Patients with coagulation and bleeding disorders 4.Sensitive to drugs being studied 5.Patient refusal

Design outcomes

Primary

MeasureTime frame
To compare duration of sensory blockade To compare duration of motor blockadeTimepoint: Sensory blockade- Time interval between onset of block (T12 dermatomal level)and two segment dermatomal regression Motor blockade- Time between onset of motor blockade(Modified Bromage scal 3) to complete regression of motor block (Modified Bromage Scale 0 )

Secondary

MeasureTime frame
Any adverse hemodynamic effects or side effectsTimepoint: Following injection of the drug intrathecally, baseline vitals will be assessed every 3 minutes for first 15 minutes & every 5 minutes thereafter till the end of procedure. Any side effects like nausea, vomiting, pruritis & sedation will also be noted;To compare onset of motor blockadeTimepoint: Time taken to reach Modified Bromage score of 3 will be assessed every 2 minutes;To compare the onset of action of sensory blockade Timepoint: Time taken to reach T12 dermatomal level assessed by sterile pin prick every 2 minutes till level reached

Countries

India

Contacts

Public ContactDr Bindu George

St. Johns Medical College

bindu575@gmail.com9342552324

Outcome results

None listed

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