Skip to main content
Clinical Trials/CTRI/2024/08/072372
CTRI/2024/08/072372Not yet recruitingNot Applicable

Comparison between ultrasound guided erector spinae plane block and ultrasound guided paravertebral block for post operative analgesia in breast surgeries- a randomised controlled study

DR SWATHI S1 site in 1 country128 target enrollmentStarted: August 28, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
128
Locations
1
Primary Endpoint
To compare the postoperative pain score using Numerical Rating Scale at 12 hours

Study Overview

Brief Summary

Comparison between ultrasound guided erector spinae plane block and ultrasound guided paravertebral block for post operative analgesia in breast surgeries as breast malignancy is the most common malignancy in female, which accounts for 25% of all cancers in women.

one of the main treatments for it is modified radical mastectomy and acute pain following breast surgery, however may result in extended hospital stay, delayed ambulation, patient discomfort. Regional anaesthesia can reduce the requirement for analgesic and anaesthetic modifications during and result in better patient outcome

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
20.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • patient wiiling to give informed written consent ASA 1 and ASA 2.

Exclusion Criteria

  • Patient not willing to give informed written consent Heart block more than 1st degree pregnancy and lactation Coagulation disorders Body Mass Index more than 35kg/m2 Patients who have known allergy to local anesthetics Heart block greater than 1st degree.

Outcomes

Primary Outcomes

To compare the postoperative pain score using Numerical Rating Scale at 12 hours

Time Frame: To compare the postoperative pain score using Numerical Rating Scale at 12 hours

Secondary Outcomes

  • 1.The time to first analgesic request(2.To compare the overall consumption of opiod{Nalbuphine} in 24 hours)

Investigators

Sponsor
DR SWATHI S
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Swathi S

ESIC Medical college and PGIMSR

Study Sites (1)

Loading locations...

Similar Trials