Skip to content

Comparing ASA and SHAPE Scores for Predicting Surgical Risk in Adults Undergoing Non-Cardiac Surgery

Evaluation of ASA Physical Status grading and SHAPE (Silverman Holt Aggregate Preoperative Evaluation) scoring for perioperative risk stratification in adult patients undergoing scheduled non-cardiac surgery: a comparative observational study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112940
Enrollment
260
Registered
2026-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Uzma Ansari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: undergoing non- cardiac surgery under general anaesthesia or regional anaesthesia.

Exclusion criteria

Exclusion criteria: Emergency (non-scheduled) surgery. Cardiac surgical procedures (including cardiac-thoracic vascular procedures). Day-case procedures not requiring overnight stay (if these are outside the study scope). Patients with incomplete preoperative assessment data or lost to follow-up within 30 days. Refusal to participate.

Design outcomes

Primary

MeasureTime frame
Primary composite outcome included the occurrence of any major postoperative complication such as cardiac events (MACE, cardiac arrest, or new arrhythmia requiring treatment), pulmonary complications , renal dysfunction ,sepsis/severe infection, stroke/TIA, or unplanned ICU admission.Timepoint: Patients were assessed at predefined time points including the preoperative period, intraoperative period, immediate postoperative period (within 24 hours), during hospital stay, and at 30-day follow-up.

Secondary

MeasureTime frame
hospital/ICU length of stay,unplanned readmission within 1 week Timepoint: Patients were assessed at predefined time points including the preoperative period, intraoperative period, immediate postoperative period (within 24 hours), during hospital stay, and at 30-day follow-up.

Countries

India

Contacts

Public ContactUzma Ansari

King Georges Medical University ,Lucknow,UP

uzma.ansari1001@gmail.com9919276838

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026