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NCT06028854 Clinical Trial

Blood Characteristics and Abdominal Emergency Surgery

Surgical Wound Clinical Trial

Official title:
Association Between Preoperative Blood Characteristics and Mortality in Abdominal Emergency Surgeries

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06028854
Other study ID # OAIC 1337/23
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 15, 2023
Est. completion date December 15, 2024

Study information
Verified date August 2023
Source University of Chile
Contact Felipe Maldonado, MD MSc
Phone +56 2 2978 8221
Email fmaldonado@uchile.cl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

After surgical tissue damage, cellular blood components are involved in tissue repair processes, yet their preoperative characteristics are not considered in routine clinical practice.

Description:

Surgical injuries initiate the recruitment of cellular blood components for tissue repair. Baseline inflammation levels and cellular response to tissue damage are absent from perioperative management algorithms despite their importance in regeneration. This project seeks to examine patients preoperative parameters before surgery and evaluate if there is a correlation with clinical outcomes.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 40
Est. completion date December 15, 2024
Est. primary completion date October 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - a) Patients between 18 and 65 years of age at the time of surgery. b) Patients with acute intra-abdominal pathology requiring emergency surgery. c) Complete blood count performed in the emergency department of our center within the 24 hours prior to surgery. Exclusion Criteria: - a) Patients who are users of anticoagulation prior to admission for any reason; b) Patients who have had previous hospitalization or surgery in the last 6 months.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Chile Hospital Clínico de la Universidad de Chile Independencia Santiago

Sponsors (1)
Lead Sponsor Collaborator
University of Chile

Country where clinical trial is conducted

Chile, 

Outcome
Type Measure Description Time frame Safety issue
Primary Death The number of deceased patients. 1 year
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