NCT07761832

Brief Summary

The goal of this observational study is to evaluate if early absolute hemoglobin decline (during the first 24 hours of admission) can predict prolonged intensive care unit stay (8 days or more) and in-hospital mortality in critically ill adult patients. The main questions it aims to answer are: Does absolute hemoglobin decline during the first 24 hours of admission independently predict prolonged intensive care unit stay in critically ill adult patients? Does absolute hemoglobin decline during the first 24 hours of admission independently predict in-hospital mortality in critically ill adult patients? Participants will: Have their routine clinical and laboratory data reviewed retrospectively from their electronic health records (including baseline hemoglobin and a second hemoglobin determination approximately 24 hours after admission). No additional interventions or extra blood draws will be performed beyond routine clinical care.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
128

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2026

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 31, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

August 3, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

August 12, 2026

Completed
Last Updated

August 12, 2026

Status Verified

August 1, 2026

Enrollment Period

Same day

First QC Date

August 3, 2026

Last Update Submit

August 10, 2026

Conditions

Keywords

critical careHemoglobinsBlood TransfusionPrognosisIntensive Care Units

Outcome Measures

Primary Outcomes (1)

  • Prolonged Intensive Care Unit Stay

    Incidence of prolonged intensive care unit (ICU) length of stay, defined a priori as an ICU stay equal to or greater than 8 days.

    From ICU admission up to 28 days

Secondary Outcomes (1)

  • In-Hospital Mortality

    From ICU admission up to 30 days

Study Arms (1)

Critically Ill Adult Patients

Adult patients admitted to the intensive care unit with an ICU stay of more than 48 hours and at least two hemoglobin determinations obtained approximately 24 hours apart during routine care.

Other: Early Absolute Hemoglobin Decline

Interventions

Measurement of the absolute difference in hemoglobin concentration (g/dL) between baseline ICU admission and approximately 24 hours post-admission. Data was collected retrospectively from electronic health records.

Critically Ill Adult Patients

Eligibility Criteria

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

dult patients admitted to the Intensive Care Unit at Hospital H+ Querétaro, Mexico, between January 2024 and January 2026, who required an ICU stay of more than 48 hours and had serial hemoglobin measurements during routine medical care.

You may qualify if:

  • Adult patients (aged 18 years or older) admitted to the Intensive Care Unit (ICU) between January 2024 and January 2026.
  • ICU length of stay greater than 48 hours.
  • At least two hemoglobin determinations obtained with an interval of approximately 24 hours apart during routine medical care.

You may not qualify if:

  • Massive bleeding upon ICU admission.
  • Massive transfusion protocol activation.
  • Pregnancy.
  • Hemoglobinopathies.
  • Active hemolytic anemia.
  • Medical records with insufficient information for analysis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital H+ Querétaro, Santiago de Querétaro, Querétaro

Querétaro City, Querétaro, 76000, Mexico

Location

MeSH Terms

Conditions

Critical IllnessAnemia

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsHematologic DiseasesHemic and Lymphatic Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 3, 2026

First Posted

August 12, 2026

Study Start

July 31, 2026

Primary Completion

July 31, 2026

Study Completion

July 31, 2026

Last Updated

August 12, 2026

Record last verified: 2026-08

Locations