Use of Macrolides in Acute Chest Syndrome: A Multicenter Retrospective Study

NCT ID: NCT07037706

Last Updated: 2025-06-25

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-06-01

Study Completion Date

2024-06-01

Brief Summary

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This study looks at whether using macrolide antibiotics is helpful and safe in treating acute chest syndrome, a serious complication in people with sickle cell disease. It reviews past cases from three hospitals where patients were treated in intensive care. The goal is to understand if macrolides make a difference, what germs are involved, how useful lab tests are, and how well patients tolerate these antibiotics.

Detailed Description

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Conditions

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Sickle Cell Disease Acute Chest Syndrome Glucose-6-Phosphate Dehydrogenase Deficiency Anti-Bacterial Agents Macrolides

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Adult patient (≥18 years old).
* Diagnosis of acute chest syndrome (ACS).
* Hospitalized in an intensive care unit (ICU).
* Microbiological sampling performed (e.g., multiplex PCR, sputum culture \[ECBC\], and/or Legionella urinary antigen test).
* Received empiric antibiotic therapy including a macrolide.

Exclusion Criteria

* Minor patient (\<18 years old).
* Acute chest syndrome not requiring ICU admission.
* Acute chest syndrome without any attempt at microbiological documentation.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier de Saint-Denis

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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France

Saint-Denis, France, France

Site Status

Countries

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France

Other Identifiers

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0063_REANIMATION

Identifier Type: -

Identifier Source: org_study_id

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