Actively Recruiting

All Genders
ID06986980

Intestinal Microsporidiosis in French Heart Transplant Recipients

Led by University Hospital, Clermont-Ferrand · Updated on 2025-07-01

39

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect and analyze data on intestinal microsporidiosis in heart transplant patients across France. Microsporidia are microscopic organisms that can cause severe diarrhea, especially in people with weakened immune systems such as organ transplant recipients. While previous studies focused on kidney and liver transplants, this study specifically examines heart transplant recipients to better understand the infection's impact and treatment in this group. The study involves a national retrospective review of epidemiological, biological, clinical, and therapeutic information from heart transplant patients diagnosed with intestinal microsporidiosis before the end of 2024. The researchers will gather data including demographics, timing of infection relative to transplant, symptoms, immunosuppressant dosage, and laboratory values at diagnosis and follow-up. Participants are not directly involved since this is an observational study using existing medical records. Researchers will evaluate outcomes such as time to clear infection, weight loss, blood cell counts, and kidney function over one year. The study helps improve understanding of this infection in heart transplant patients and may inform future care. The total duration of follow-up for data collection is one year after diagnosis, with some measurements taken at three months.

CONDITIONS

Brief Title

Intestinal Microsporidiosis in French Heart Transplant Recipients (CARMIC)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Heart transplant patients diagnosed with intestinal microsporidiosis
  • Diagnosis made before December 31, 2024 in France (metropolitan France and overseas territories)
Not Eligible

You will not qualify if you...

  • Patient opposition

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 year

Participants have data collected related to their diagnosis of intestinal microsporidiosis including clinical, biological, and demographic information.

1 to 2 visits depending on timing of diagnosis

Long-term Monitoring

Duration - 3 months

Participants are observed over time to collect follow-up data including blood tests and clinical status for up to 3 months after diagnosis.

Visits at Day 0 (diagnosis) and Month 3

Trial Site Locations

Total: 1 location

1

CHU Gabriel Montpied

Clermont-Ferrand, France, 63000

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Research Team

L

Lise Laclautre

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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