A CLINICAL STUDY TO COMPARE THE EFFICACY OF INTRATHECAL LEVOBUPIVACAINE AND BUPIVACAINE IN SPINAL ANESTHESIA.

A RANDOMIZED CONTROLLED TRIAL TO COMPARE THE CLINICAL EFFICACY OF INTRATHECAL PLAIN LEVOBUPIVACAINE AND BUPIVACAINE IN SPINAL ANESTHESIA FOR THE PATIENTS UNDERGOING INFRAUMBLICAL SURGERY

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2016/10/007342

Enrollment

100

Registered

2016-10-06

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: levobupivacaine: 3ml of 0.5% intrathecal isobaric levo bupivacaine Control Intervention1: hyperbaric bupivacaine: 3 ml of 0.5% intrathecal hyperbaric bupivacaine Control Intervention2:

Eligibility

Inclusion criteria

Inclusion criteria: • ASA Grade I and II patients. • Age group 18-60 yrs • Height > 145 cms • Weight

Exclusion criteria

Exclusion criteria: • Any contradiction to regional anaesthesia • Have a known allergy to local anaesthetics • Showing dysrrythmmias in the ECG • Severe psychiatric disturbance

Design outcomes

Secondary

Measure	Time frame
onset and duation of sensory and motor block. incidence of hypotension and bradycardia and other side effects.Timepoint: 24hrs	—

Primary

Measure	Time frame
Quality of surgical anaesthesia graded as excellent, good or poor depending upon the response of the patient and the requirement of additional analgesia.Timepoint: 24HRS	—

Countries

India

Contacts

Public ContactAJAY SINGH

LADY HARDINGE MEDICAL COLLEGE,NEW DELHI

anug71@yahoo.co.in9711000264

Outcome results