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Comparison of hemodynamic profile of 0.5% hyperbaric Levobupivacaine and 0.5% hyperbaric Bupivacaine for spinal anaesthesia

Comparison of hemodynamic profile of 0.5% hyperbaric Levobupivacaine and 0.5% hyperbaric Bupivacaine in patients undergoing Lower Limb Arthroscopic Surgeries under spinal anaesthesia, a prospective randomized control study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/071977
Enrollment
100
Registered
2024-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M999- Biomechanical lesion, unspecified Health Condition 2: M999- Biomechanical lesion, unspecified Health Condition 3: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: 0.5% hyperbaric Levobupivacaine: is a local anesthetic similar to bupivacaine but is the S(-)-enantiomer of bupivacaine. It is the spinal anaesthetic drug expected to have better haemo

Sponsors

Vikram C
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade 1 and 2 Patients undergoing lower limb arthroscopic surgeries under spinal anaesthesia

Exclusion criteria

Exclusion criteria: Patients who are unwilling Known hypersensitivity to any of the test drug Any contraindication to spinal anaesthesia Cardiac arrythmias/ severe cardiac disease

Design outcomes

Primary

MeasureTime frame
To compare the hemodynamic effects between 0.5% Hyperbaric Bupivacaine and 0.5% Hyperbaric LevobupivacaineTimepoint: Intraoperative hemodynamic parameters (BP, HR, and MAP) will be assessed at 1 minute before (baseline) and 1, 2, 3, and 5 minutes after the induction of spinal anesthesia. Thereafter, measurements will be performed in 5-minute intervals during the first 30 minutes of surgery and then every 10 minutes until the end of the surgery.

Secondary

MeasureTime frame
1.Duration of analgesia 2.Sensory and motor block onset 3. Segmental height of block 4. Adverse eventsTimepoint: 1.Total duration of analgesia in minutes. 2.The degree of motor block onset in the lower limbs will be assessed at 5 min, 10 min, and 15 min using a modified Bromage scale (MBS). Highest sensory block level attained was checked by using the pinprick method 3.Maximum segmental height block after 15min. 4.Any adverse events noted during entire anaesthesia.

Countries

India

Contacts

Public ContactVidhu Bhatnagar

Institute of Naval Medicine, INHS ASVINI

vizardsvids@gmail.com99697771668

Outcome results

None listed

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