- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04934202
Cohort Follow-up of Survivors of Hospitalization for COVID-19 During the 2nd Wave of the Epidemic in France (COMEBAC 2)
Cohort Follow-up at 6-12 Months of Survivors of Hospitalization for COVID-19 During the 2nd Wave of the Epidemic From a University Hospital in France
연구 개요
상세 설명
From 15th July to 18th September, 2020, in a first uncontrolled cohort study (Multi-Expertise Consultation of Bicêtre After Covid-19, COMEBAC), we evaluated at four months the surviving patients who were hospitalized at the Bicêtre hospital for COVID-19 during the 1st wave of the epidemic in France and having survived this hospitalization. This cohort included 478 patients. The article resulting from the analysis of the data collected is accepted for publication in JAMA.
This evaluation, the aim of which was both clinical and scientific, was carried out largely thanks to human and material resources then demobilized because of the epidemic and thanks to the investment of doctors and psychologists who carried out the work in addition to their usual work.
The response to the current call for projects aims to bring together the means to continue this monitoring work during the 2nd epidemic wave, while the means and staff are this time completely mobilized by the care of patients with COVID-19 and other. It also aims to raise funds that will allow an in-depth analysis of the residual symptoms presented by the patients.
The current project aims to continue the work started with the COMEBAC "1st wave" cohort with:
- The inclusion of patients hospitalized after the 1st wave.
- An assessment of symptoms according to the SARS-CoV-2 variant.
- A 12-month follow-up of symptomatic patients during the evaluation in COMEBAC "1st wave".
연구 유형
등록 (예상)
연락처 및 위치
연구 연락처
- 이름: Tai PHAM
- 전화번호: +33145217245
- 이메일: tai.pham@aphp.fr
연구 장소
-
-
-
Le Kremlin-Bicêtre, 프랑스, 94270
- 모병
- Bicetre Hospital
-
연락하다:
- Tai PHAM
- 전화번호: 0145217245
- 이메일: tai.pham@aphp.fr
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
For the 6-month evaluation of patients from the 2nd epidemic wave
Inclusion criteria
- Age ≥18 years old
- COVID-19 defined either by a reverse transcriptase-polymerase chain reaction (RT-PCR) or by a combination of clinical signs and compatible lung CT scan
- Hospitalization for COVID-19 after 1st July 2020
- Living out of the hospital
Exclusion criteria
- Death occurring between index hospitalization and reassessment
- Patient refusal
- Discovery of a positive RT-PCR for SARS-CoV-2 during hospitalization for a reason other than COVID-19
- Nosocomial COVID-19
For the 12-month evaluation of patients from the 1st epidemic wave
Inclusion criteria
◌ Presence of general, cognitive, psychological and respiratory symptoms during the assessment made at 4 months in COMEBAC "1st wave"
Exclusion criteria
- Death occurring between the evaluation in COMEBAC "1st wave" and the re-evaluation
- Patient refusal
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
Patients from the 1st epidemic wave
One year after their discharge from the initial hospitalization, patients who presented symptoms during the evaluation in COMEBAC "1st wave" in summer 2020 will benefit from a telephone assessment on the same schedule as that detailed above.
If symptoms persist, they will be called to the day hospital for an assessment similar to the one detailed above.
|
Teleconsulting physicians will subject patients to a standardized questionnaire that will look for the following symptoms:
Edition 2021 ◌ Cognitive signs using the Q3PC questionnaire (10): memory loss, slowness in reasoning, activity planning or problem solving, concentration, attention difficulties During a day hospitalization planned during the teleconsultation, patients will benefit from the following multidisciplinary assessment.
|
|
Patients from the 2nd epidemic wave
As during the evaluation carried out during the 1st wave, the detection of persistent symptoms will be done in two stages:
|
Teleconsulting physicians will subject patients to a standardized questionnaire that will look for the following symptoms:
Edition 2021 ◌ Cognitive signs using the Q3PC questionnaire (10): memory loss, slowness in reasoning, activity planning or problem solving, concentration, attention difficulties During a day hospitalization planned during the teleconsultation, patients will benefit from the following multidisciplinary assessment.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Prevalence of respiratory, cognitive and psychological symptoms presented at 6 months of hospitalization for COVID-19.
기간: 6 months
|
nature and prevalence of symptoms persisting at 6 months of an episode of COVID-19 requiring hospitalization
|
6 months
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Difference between the prevalence of residual symptoms between patients hospitalized during the 1st wave of the epidemic in France (from the COMEBAC "1st wave" study) and those of the current study
기간: 6 months
|
risk factors for the various sequelae of COVID-19
|
6 months
|
|
Association between patient characteristics and the prevalence of residual symptoms.
기간: 6 months
|
effect of the therapeutic changes that occurred between the 1st and 2nd wave of COVID-19 on these persistent symptoms.
|
6 months
|
|
Association between residual symptoms and the type of SARS-CoV-2 variant
기간: 6 months
|
residual symptoms of COVID-19 according to the SARS-CoV-2 variants responsible
|
6 months
|
|
Prevalence of respiratory, neurological, cognitive and psychological symptoms presented at 6 months of hospitalization for COVID-19 which occurred during the 1st epidemic wave.
기간: 6 months
|
residual symptoms of COVID-19 one year after COVID-19 that occurred during the 1st epidemic wave
|
6 months
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Tai PHAM, Bicetre Hospital
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- COMEBAC 2
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .