NCT05066386

Brief Summary

Retrospective observational study on the effects of altering components of RCRI to improve the predictive capacity.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20,099

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2013

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2013

Completed
8.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2021

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 20, 2021

Completed
14 days until next milestone

First Posted

Study publicly available on registry

October 4, 2021

Completed
Last Updated

October 4, 2021

Status Verified

October 1, 2021

Enrollment Period

8.5 years

First QC Date

September 20, 2021

Last Update Submit

October 1, 2021

Conditions

Keywords

HbA1C: Hemoglobin ratio (HH ratio)Risk modelRCRI

Outcome Measures

Primary Outcomes (1)

  • Mortality

    To compare the predictive value of RCRI and substitution of the "DM on insulin" component with HH ratio for 30- and 90-day mortality

    90 days

Secondary Outcomes (1)

  • Morbidity

    7 days

Interventions

The objective of the study is to compare the predictive value of RCRI and substitution of the "DM on insulin" component with HH ratio for 30- and 90-day mortality, and postoperative acute myocardial injury(AMI) and acute kidney injury(AKI).

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients undergoing non cardiac surgery in Singapore General Hospital

You may not qualify if:

  • If patient is below 18 years old
  • no History of DM
  • No HbA1C done within 3 months prior to date of surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 20, 2021

First Posted

October 4, 2021

Study Start

January 1, 2013

Primary Completion

July 1, 2021

Study Completion

August 1, 2021

Last Updated

October 4, 2021

Record last verified: 2021-10

Data Sharing

IPD Sharing
Will not share

Due to patient identifiers present in the dataset. Sensitive dataset