A Study of Ropivacaine versus Bupivacaine under Spinal Anaesthesia in Lower Abdominal and Lower Limb Surgeries

A Comparative Study of 0.75% Hyperbaric Ropivacaine versus 0.5% Hyperbaric Bupivacaine under Spinal Anaesthesia in Lower Abdominal and Lower Limb Surgeries - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065441

Enrollment

Registered

2024-04-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

None listed

Interventions

Intervention1: Spinal Anaesthesia with hyperbaric Ropivacaine: Subarachnoid block will be given with 3ml of 0.75% hyperbaric Ropivacaine using 25 G Quinckes needle in left lateral position with midlin

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I or II, 18-60 years, either sexes, 50-70 kgs, patients for lower abdominal and lower limb surgeries

Exclusion criteria

Exclusion criteria: Negative consent, surgery more than 3hrs, drug sensitivity, disease or deformity of spine, infection at puncture site, coagulation disorders, pregnant/lactating, psychiatric patients

Design outcomes

Primary

Measure	Time frame
To compare the onset, duration and level of sensory blockade achieved after intrathecal administration of the two drugs.Timepoint: Intraoperative period after spinal anesthesia	—

Secondary

Measure	Time frame
To compare the characteristics of spinal block and hemodynamic changes among the two study groupsTimepoint: Intraoperative and post operative period after SA	—

Countries

India

Contacts

Public ContactMEHAK DUREJA

MM Institute of Medical Sciences and Research Centre

mehakdureja@gmail.com9530835730

Outcome results