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FOLLOW-UP OF PATIENTS WITH COVID-19.

TeleRea'nCo : FOLLOW-UP OF PATIENTS WITH COVID-19.

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04609839
Acronym
TeleRea'nCo
Enrollment
0
Registered
2020-10-30
Start date
2020-09-15
Completion date
2023-10-17
Last updated
2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patient Admitted to Intensive Care Unit for COVID-19

Brief summary

Some patients admitted to intensive care for a severe form of COVID-19 could have respiratory, cardiac, renal and neurological sequelae in the medium or long term. The results of this research will allow an improvement in the understanding and management of patients in the medium and long term.

Interventions

OTHERFollow-up of patients with COVID-19

The presence of sequelae, number of re-hospitalizations, date of death and cost of health expenditure will be collected. The Quality of life score (SF-36 questionnaire) and the Pittsburgh sleep quality index (PSQI questionnaire) will be completed by patients.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient admitted to intensive care unit for COVID-19 * Adult patient ≥ 18 years old * Subject having expressed his non-opposition to the research * Subject affiliated to a social health insurance protection scheme or beneficiary of such a scheme

Exclusion criteria

* Subject under safeguard of justice * Patient under guardianship or curatorship

Design outcomes

Primary

MeasureTime frame
The presence of respiratory, renal, cardiac, motor, neurological, and psychological sequelae will be assessed by specialist doctors during the 12 months following the patient's discharge from intensive care.The primary endpoint will be measured during 12 months following the patient's discharge from intensive care.

Secondary

MeasureTime frame
1) The sequelae by type of impairment will be assessed by specialist doctors at 3, 6 and 12 monthsAt M3 (+/-15 days) : 3 months after patient inclusion-At M6 (+/-15 days) : 6 months after patient inclusion-At M12 (+/-15 days) : 12 months after patient inclusion
2) Number of re-hospitalizations at 3, 6 and 12 monthsAt M3 (+/-15 days) : 3 months after patient inclusion-At M6 (+/-15 days) : 6 months after patient inclusion-At M12 (+/-15 days) : 12 months after patient inclusion
3) Date of deathDate of death will be collected from inclusion to M12 (12 months after patient inclusion)
4.1) Quality of life score (SF-36 questionnaire) at 3, 6 and 12 monthsAt M3 (+/-15 days) : 3 months after patient inclusion-At M6 (+/-15 days) : 6 months after patient inclusion-At M12 (+/-15 days) : 12 months after patient inclusion
4.2) The Pittsburgh sleep quality index (PSQI questionnaire) at 3, 6 and 12 monthsAt M3 (+/-15 days) : 3 months after patient inclusion-At M6 (+/-15 days) : 6 months after patient inclusion-At M12 (+/-15 days) : 12 months after patient inclusion
5) Cost of health expenditureThe cost of health expenditure will be collected from inclusion to M12 (12 months after patient inclusion)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026