to study the Efficacy of pain relief from erector spinae plane block for patients undergoing abdominal surgery

Not Applicable

• Conditions: Health Condition 1: K353- Acute appendicitis with localizedperitonitisHealth Condition 2: K810- Acute cholecystitisHealth Condition 3: K400- Bilateral inguinal hernia, with obstruction, without gangreneHealth Condition 4: N72- Inflammatory disease of cervix uteri

• Registration Number: CTRI/2022/06/043314
• Lead Sponsor: JLN MEDICAL COLLEGE AJMER

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 27 June 2022

Recruitment & Eligibility

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

Inclusion Criteria

Age group between 18 and 60 years, Body weight 30 to 80kg , Patients belonging to ASA (American Society of Anaesthesiologists) class 1 and 2 Patients undergoing

abdominal surgery of duration 1 to 2 hours in theatre with

haemoglobin atleast 9 gm/dl, Patient free from any associated

acute or chronic systemic illness

Exclusion Criteria

Patients not willing to participate in the study

Uncooperative patients

Patient with chronic pain or on long-term analgesics

Any known hypersensitivity or contraindication to bupivacaine

Local pathology at the site of injection or disability limiting the

performance of block,(deformity of spine)

Patients receiving beta blockers or cardiac drugs.

History of convulsion, allergy to the drug used, bleeding disorder,

severe neurological deficit, thyroid disorder

Patient with history of respiratory, cardiac, hepatic or renal disease

(necessitating classification in ASA Class III or above)

Patients having a history of significant neurological, psychiatric, or

neuromuscular disorders

Pregnant, lactating mothers

Study & Design

• Study Type: Interventional
• Study Design: Not specified