NCT06792578

Brief Summary

Surgical start times significantly impacted mortality, morbidity, and resource utilization, particularly in high-risk patients.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
291,051

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

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

June 3, 2022

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

January 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 24, 2025

Completed
Last Updated

January 27, 2025

Status Verified

June 1, 2022

Enrollment Period

2.6 years

First QC Date

January 20, 2025

Last Update Submit

January 23, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • 30-Day Postoperative Mortality

    "The primary outcome measure is the incidence of 30-day postoperative mortality in patients undergoing non-cardiac surgeries. Mortality is defined as death occurring within 30 days following the surgery. The study aims to evaluate the association between surgical start times (morning, afternoon, and nighttime) and the risk of mortality

    30 days post-surgery

Interventions

This intervention focuses on the retrospective analysis of the association between surgical start times (morning, afternoon, and nighttime) and postoperative outcomes in non-cardiac surgeries. The study evaluates how the timing of surgery impacts mortality, complications, transfusion rates, and ICU admissions in a tertiary hospital setting

Eligibility Criteria

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

The study population includes adult patients aged 18 years or older who underwent elective non-cardiac surgeries at a tertiary hospital. Patients with emergency surgeries, incomplete data on surgical start times, or missing follow-up information were excluded from the analysis. The study focuses on evaluating the impact of surgical start times (morning, afternoon, and nighttime) on postoperative outcomes, including mortality, complications, and ICU admission.

You may qualify if:

  • Patients aged 18 years or older
  • Patients who underwent non-cardiac surgery

You may not qualify if:

  • Emergency surgeries
  • Cadaver surgeries
  • Transplantation surgeries
  • Patients with incomplete or missing data, such as follow-up information, operation start times, or laboratory values

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Asan Medical Center

Seoul, Seoul, 05505, South Korea

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 20, 2025

First Posted

January 24, 2025

Study Start

June 3, 2022

Primary Completion

December 30, 2024

Study Completion

January 20, 2025

Last Updated

January 27, 2025

Record last verified: 2022-06

Data Sharing

IPD Sharing
Will not share

The dataset used and/or analyzed during the current study is available from the corresponding author upon reasonable request.

Locations