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Clinical Trials/CTRI/2020/11/029140
CTRI/2020/11/029140Not yet recruitingNot Applicable

Comparative evaluation of analgesic efficacy of different concentrations of Levobupivacaine In Ultrasound Guided Erector Spinae Block For Breast Surgery

DrKewal Krishan Gupta1 site in 1 country60 target enrollmentStarted: November 16, 2020Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
TOTAL DURATION OF ANALGESIA WILL BE NOTED IN TWO GROUPS POSTOPERATIVELY .IT WILL BE TAKEN FROM TIME OF COMPLETION OF INJECTION TO THE REQUEST OF FIRST RESCUE ANALGESIA

Study Overview

Brief Summary

total of 60 patients will be randomly allocated into 2 study groups of 30 patients each .Each group will receive erector spinae block before induction with general anesthesia technique .Group A will recevie 20ml of 0.25%levobupivacaine and Group B will receive 20ml of 0.375% levobupivacaine . Duration of postoperative analgesia in first 24 hours postoperatively will be noted and compared .After completion of study ,observation obtained will be tabulated and analysed using appropriate stastical methods. .

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Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Not Applicable

Eligibility Criteria

Ages
20.00 Year(s) to 65.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • ASA I AND II PATIENTS PATIENTS SCHEDULED FOR BREAST SURGERY.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

TOTAL DURATION OF ANALGESIA WILL BE NOTED IN TWO GROUPS POSTOPERATIVELY .IT WILL BE TAKEN FROM TIME OF COMPLETION OF INJECTION TO THE REQUEST OF FIRST RESCUE ANALGESIA

Time Frame: In the first 24 hours of postoperative period

Secondary Outcomes

  • QUALITY OF ANALGESIA(in postoperative period at 0,2‚4‚8‚12‚18‚24hours)

Investigators

Sponsor
DrKewal Krishan Gupta
Sponsor Class
Other [Guide has ensured that all the facilities for the study are available in the institution ]

Study Sites (1)

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