comparing doses of drug required through two different technique of paravertebral block for pain relief after breast surgery

Not Applicable

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2023/02/049389
• Lead Sponsor: swarnika singh

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 February 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.female

2.aged 18 to 80 years

3.American Society of Anesthesiologists (ASA) physical status I to III

4.scheduled for unilateral mastectomy surgery, with or without axillary node dissection

5.able to give informed consent

6.able to cooperate with the study process

Exclusion Criteria

1.Patient refusal

2.allergy to LA and other medications used in the study

3.bilateral mastectomies

4.coexisting hematologic disorder

5.having deranged coagulation parameters

6.preexisting major organ dysfunction such as hepatic and renal failure (glomerular filtration rate <60 mL/min per 1.73 m2)

7.significant thoracic kyphoscoliosis;

8.history of previous thoracic surgery

9.Inability to communicate and cooperate

Study & Design

• Study Type: Interventional
• Study Design: Not specified