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

Not yet recruiting

Conditions: Bilateral inguinal hernia, with obstruction, without gangrene, (2) ICD-10 Condition: K353||Acute appendicitis with localizedperitonitis, (3) ICD-10 Condition: N72||Inflammatory disease of cervix uteri, (4) ICD-10 Condition: K810||Acute cholecystitis,

Registration Number: CTRI/2022/06/043314

Lead Sponsor: JLN MEDICAL COLLEGE AJMER

Brief Summary: Aim of our study is to assess the efficacy of erector spinae plane block (ESPB) for post operative analgesia in patients undergoing abdominal surgery under general / spinal anaesthesia using Ropivacaine (0.25%) with dexmedetomidine by creating a comparison with those without the block

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 70

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

Primary Outcome Measures

Name	Time	Method
Comparison of Number and frequency of	Around 1 year
postoperative analgesia required in both the	Around 1 year
groups for First 36 hours Postoperatively	Around 1 year
To assess the effective analgesia by visual	Around 1 year
analog scale (VAS) score	Around 1 year

Secondary Outcome Measures

Name	Time	Method
to assess hemodynamic changes	to assess and compare the adverse effect

Trial Locations

Locations (1): JLN medical college
🇮🇳
Ajmer, RAJASTHAN, India
JLN medical college
🇮🇳Ajmer, RAJASTHAN, India
Dr suneel ganganna ampragundi
Principal investigator
9743383462
suneelga628@gmail.com