Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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SUSPENDED
40 participants
OBSERVATIONAL
2025-10-15
2027-12-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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High Neutrophil count
Patients with high neutrophil count in their preoperative complete blood count
No interventions assigned to this group
Low Neutrophil count
Patients with low neutrophil count in their preoperative complete blood count
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with acute intra-abdominal pathology requiring emergency surgery.
* A complete blood count was performed in the emergency department of our center within 24 hours before surgery.
Exclusion Criteria
* Patients who have had previous hospitalization or surgery in the last 6 months.
18 Years
65 Years
ALL
Yes
Sponsors
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University of Chile
OTHER
Responsible Party
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Principal Investigators
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Felipe Maldonado
Role: STUDY_CHAIR
Hospital Clinico de la Universidad de Chile
Locations
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Hospital Clínico de la Universidad de Chile
Independencia, Santiago Metropolitan, Chile
Hospital Clínico Universidad de Chile
Santiago, Santiago Metropolitan, Chile
Countries
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Other Identifiers
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OAIC 1337/23
Identifier Type: -
Identifier Source: org_study_id