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NCT04010474 Clinical Trial

Surgical APGAR Score and Modified Surgical APGAR Score

Perioperative/Postoperative Complications Clinical Trial

Official title:
Comparison of Surgical APGAR Score and Modified Surgical APGAR Score in Predicting Possible Postoperative Complications in Major Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04010474
Other study ID # 09.05.2017 658
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2017
Est. completion date October 30, 2017

Study information
Verified date July 2019
Source Okmeydani Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study we aimed to define a new modified SAS is to predict the incidence of postoperative complication and mortality in major abdominal and orthopedic surgery. We also identify the effectivity of this modified scoring system composed of the duration of operation in addition to the three intraoperative parameters of SAS.

Recruitment information / eligibility
Status Completed
Enrollment 308
Est. completion date October 30, 2017
Est. primary completion date September 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subject has major surgery

- More than 18 years

Exclusion Criteria:

- Pregnant

- Younger than 18

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Modified Surgical APGAR Score
Four intraoperative factors Lowest heart rate (HR), Lowest mean arterial pressure (MAP) Estimated blood loss Operation time

Locations
Country Name City State
Turkey Namigar Turgut Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Namigar Turgut

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Comparison of Surgical APGAR Score and Modified Surgical APGAR Score in Predicting Possible Postoperative Complications in Major Surgery Operation time should be included as a simple, objective and practical indication of the SAS risk score in the major operations in our study including a single-center, prospective 308 case study, as it can be seen as an independent predictor of postoperative mortality and complications. 01.06.2017 - 30.09.2017
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