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Risk assessment after abdominal surgery using a scoring involving change in heart rate,blood pressure and total blood loss during surgery

Not Applicable
Conditions
Health Condition 1: K669- Disorder of peritoneum, unspecified
Registration Number
CTRI/2019/02/017567
Lead Sponsor
SVIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All elective and emergency open abdominal surgeries

Patients with age 18 year-75 year of either sex

Patients of American Society of Anesthesiologists physical status (ASA PS)1-5 including E

Patients who are willing to participate in the study

Exclusion Criteria

Patients with age less than 18year and more than 75year,

Patients undergoing mini laparotomy or laparoscopic surgery.

Patients with established metastatic and/or unresectable tumours,

Patients who are unwilling to participate in the study.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total number of mortality during 30 days observation period <br/ ><br>To determine the proportion of patients undergoing elective and emergency surgical procedures who develop major complications during the 30-day post-operative period.Timepoint: 30 days after surgery
Secondary Outcome Measures
NameTimeMethod
Total number of mortality during 30 days observation periodTimepoint: 30 days after surgery
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