Comparison of levobupivacaine heavy and Ropivacaine heavy in geriatric population undergoing lower limb surgeries

A comparative study of hyperbaric levobupivacaine and hyperbaric Ropivacaine in spinal anesthesia in lower limb surgeries of geriatric patients - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/062549

Enrollment

Registered

2024-02-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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: spinal anesthesia: Intrathecal hyperbaric levobupivacaine 0.5% (15mg) and hyperbaric ropivacaine 0.75%(22.5mg) used as local anesthetic agent for spinal anesthesia for one time to carry

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1/2/3 included of age 60-85 years being admitted to orthopedic ward of Tezpur medical college and hospital.

Exclusion criteria

Exclusion criteria: if patient refuses to participate,known allergy,belong to ASA 4,requiring emergency surgery,infection at the block site,known coagulopathy or on anticoagulant therapy,morbid abesity,and in lactating/pregnant women

Design outcomes

Primary

Measure	Time frame
hemodynamic stability in each study groupsTimepoint: hemodynamic stability in each study groups for 180 minutes	—

Secondary

Measure	Time frame
onset & duration of sensory block, duration of motor block of both drugsTimepoint: time point will be same as primary outcome that is 180 minutes	—

Countries

India

Contacts

Public ContactAnubh gupta

tezpur medical college and hospital

drjagadishbasumatary@gmail.com6392601373

Outcome results

None listed

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