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A Study on How Different Risk Assessment Tools Predict Recovery and Complications in Patients Undergoing Emergency Surgeries

Comparative Analysis and Evaluation of Risk Stratification Indices based on recent guidelines for Perioperative Outcomes in Emergency Surgeries: A Prospective Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/06/089185
Enrollment
93
Registered
2025-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: T07- Unspecified multiple injuries

Interventions

Intervention1: Nil: Nil

Sponsors

NONE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Surgical Procedure: Any emergency surgery (gastrointestinal, vascular, urological, gynecological, trauma, etc.) Consent: Written informed consent ASA Classification: ASA I-IV E Hospital Admission: Patients admitted for emergency surgical intervention Risk Index Applicability: Cases where RCRI, NSQIP, and SORT can be applied

Exclusion criteria

Exclusion criteria: Severe Coagulopathy: Patients with severe bleeding disorders (e.g., hemophilia, DIC) Pregnancy & Lactation Incomplete Medical Records: Missing data affecting risk index calculation Non-Compliance: Patients unable to adhere to the study protocol or follow-up Emergency Cardiac or Neurological Surgeries

Design outcomes

Primary

MeasureTime frame
To compare the predictive accuracy of individual risk indices (RCRI, NSQIP, SORT) for adverse perioperative outcomes in emergency surgeriesTimepoint: Timepoints mentioned Preoperative: Risk scores via RCRI, NSQIP, SORT. Intraoperative: Monitor for hemodynamic instability, arrhythmias, blood loss, hypoxia. Post-op (48 hrs): Check for MI, AKI, respiratory events, unplanned ICU. Post-op (30 days): Track SSIs, VTE, pulmonary issues, readmissions, mortality.

Secondary

MeasureTime frame
To evaluate the predictive accuracy of each risk index for intraoperative complications (e.g., hemodynamic instability, arrhythmias, significant blood loss requiring transfusion, and hypoxiaTimepoint: ;To assess the accuracy of each risk index in predicting immediate postoperative outcomes within 48 hours (e.g., postoperative nausea and vomiting [PONV], respiratory complications [e.g., aspiration pneumonitis, pneumonia], acute kidney injury [AKI], and unplanned ICU admissions).Timepoint: For first 48 hours post operation;To evaluate the predictive power of each risk index for delayed postoperative complications up to 30 days (e.g [SSI], cardiovascular events [e.g., myocardial infarction, arrhythmias], pulmonary complications [e.g., pneumonia, pulmonary embolism], thromboembolic events [e.g., deep vein thrombosis, pulmonary embolism], transfusion-related complications, and hospital readmissions).Timepoint: For 30 days post operation;To identify the most reliable risk index for perioperative risk stratification in emergency surgeries By comparing their sensitivity, specificity, and overall predictive performance for all phases (intraoperative, immediate, and delayed postoperative outcomes).Timepoint:

Countries

India

Contacts

Public ContactDr Bhavna Gupta

All India Institute of Medical Sciences Rishikesh

bhavna.kakkar@gmail.com7534987302

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026