A study to compare 0.75% hyperbaric ropivacaine & 0.5% levobupivacaine in spinal anaesthesia for patients undergoing infraumblical surgeries

A comparative evaluation of 0.75% hyperbaric ropivacaine & 0.5% levobupivacaine in spinal anaesthesia for patients undergoing infraumblical surgeries- A randomized double blind study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/07/054993

Enrollment

Registered

2023-07-10

Start date

Unknown

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

Health Condition 1: N399- Disorder of urinary system, unspecified Health Condition 2: S828- Other fractures of lower leg Health Condition 3: S798- Other specified injuries of hip and thigh Health Condition 4: S899- Unspecified injury of lower leg

Interventions

Intervention1: 0.75% hyperbaric ropivacaine: 3ml of 0.75% hyperbaric ropivacaine administered and the study parameters noted till the effect of the drug is regressed Control Intervention1: 0.5% hyperb

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing elective infraumbilical surgeries under spinal anaesthesia who fit into American Society of Anaesthesiologists (ASA) physical status I and II.

Exclusion criteria

Exclusion criteria: Contraindications to spinal anaesthesia Patient refusal Patient allergic to opioids and local anaesthetic agents Pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
To compare the effect on onset & duration of sensory block & onset & duration of motor blockTimepoint: The block will be assessed at 1 minute interval for the first 10 minutes,every 5 minutes in the first hour, every 10 minutes till the regression of block	—

Secondary

Measure	Time frame
To compare the effect on hemodynamic changes in both the groupsTimepoint: Hemodynamic parameters measured every 2 minute time intervals for the first 10 minutes followed by 5 minute intervals for the next 20 minutes & at 10 minute intervals till the end of the surgery	—

Countries

India

Contacts

Public ContactSandya Rani DC

M S Ramaiah Medical College

drsandyarani@gmail.com9886127243

Outcome results

None listed

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