Longitudinal Observational Study for mIddle Term Follow-up Patients Admitted for Acute Dyspnea in TunIsia

NCT04947358 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 180

Last updated 2021-07-01

No results posted yet for this study

Summary

The purpose of the SIDI study is to follow, few months after discharge from the hospital, the patients admitted to the 3 emergency departments in Tunisia for acute dyspnea and to determine the proportion and the factors favoring rehospitalization and death.

Conditions

  • Longitudinal Observational Study With 6 Months Follow-up

Sponsors & Collaborators

  • S Form Pharma

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-22
Primary Completion
2021-12-30
Completion
2021-12-30

Countries

  • Tunisia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04947358 on ClinicalTrials.gov