Use of nerve block for after surgery pain relief in breast surgery.

Phase 3

Not yet recruiting

• Conditions: Breast tumour

• Registration Number: CTRI/2018/03/012712
• Lead Sponsor: Indira Gandhi Institute of medical Sciences

Brief Summary

To see the effect of erector spinae plane block for postoperative analgesia  in reducing morphine requirement after breast surgery. Patient would be monitored postoperatively every 4 hours on NRS Scale. There would be two group one would receive analgesia by erector spinae block other would be cantrol group.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2018-03-21
• Study Start: 2018-03-31

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 40

Inclusion Criteria

Patients posted for breast surgery (Modified Radical Masectomy, Simple mastectomy, Lumpectomy) ASA grade 1,2,3.

Exclusion Criteria

ASA grade 4 Any allergy to local anaesthetics Patients refusal Infection at site of intervention.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperatively for 24 hours total opioid consumption.	Every 4 hours for 24 hrs

Secondary Outcome Measures

Name	Time	Method
Sensory block - loss of cold sensation of anterior and posterior roots of thoracic spinal nerve dermatomes	Pain scores – numerical rating scores (NRS) will be used

Trial Locations

Locations (1)

Indira Gandhi Institute of Medical Sciences; 🇮🇳 Patna, BIHAR, India

Indira Gandhi Institute of Medical Sciences

🇮🇳Patna, BIHAR, India

GUNJAN KUMAR

Principal investigator

7352360745

bkpgunjankr@gmail.com