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sefullness of ultrasound guided bilateral erector spinae block in diminishing pneumoperitoneal strect pain response in patients undergoing laparoscopic abdominal surgeries under general anesthesia

Not Applicable
Conditions
Health Condition 1: K812- Acute cholecystitis with chronic cholecystitis
Registration Number
CTRI/2021/12/038716
Lead Sponsor
Dr NAMRATHA C
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients belonging to ASA1 and 2

Patients undergoing laparoscopic abdominal surgeries under general anesthesia

Exclusion Criteria

Patients having serious systemic illness

Hypersensitivity to drugs

Laparoscopic Surgeries getting converted to open surgeries

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To campare pneumoperitoneal strech response in terms of HR and MAP in patients undergoing laparoscopic abdominal surgeries under general anesthesiaTimepoint: To campare pneumoperitoneal strech response in terms of HR and MAP in patients undergoing laparoscopic abdominal surgeries under general anesthesia at 5 min, 10 min 20 min 30 min,60min after pneumoperitoneum
Secondary Outcome Measures
NameTimeMethod
To campare requirement of opioids intra operativelhTimepoint: Entire duration of the procedure
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