이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Cohort Follow-up of Survivors of Hospitalization for COVID-19 During the 2nd Wave of the Epidemic in France (COMEBAC 2)

2021년 6월 18일 업데이트: Assistance Publique - Hôpitaux de Paris

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

From July to September 2020, in a first uncontrolled cohort study, 478 patients who were hospitalized at Bicêtre hospital for COVID-19 and who survived were evaluated at 4 months (publication accepted at JAMA). The current project aims to bring together the means to continue this work during the 2nd epidemic wave.

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

관찰

등록 (예상)

500

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

      • Le Kremlin-Bicêtre, 프랑스, 94270
        • 모병
        • Bicetre Hospital
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

Patients from the 1st epidemic wave Patients from the 2nd epidemic wave

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

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

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:

  • General signs: Anorexia, fatigue, new hospitalization, weight loss,
  • Respiratory signs: recent dyspnoea, chest discomfort, chest pain, new cough, abnormal lung CT scan since discharge
  • Neurological signs: headache, paraesthesia, anosmia, limb paralysis
  • Digestive signs: abdominal pain, diarrhoea, constipation, nausea, vomiting

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.

  • General clinical examination
  • Assessment of the state of health
  • Respiratory assessment
  • Pulmonary CT assessment
  • Cognitive evaluation
  • Cardiological evaluation
  • Renal assessment
  • Immunological evaluation
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:

  • During a teleconsultation, to which all eligible patients will be invited, systematically looking for general, neurological, cognitive and respiratory symptoms
  • During a hospitalization in an outpatient clinic to which all survivors who have stayed in an intensive care unit (ICU) will be invited and, among patients who have not stayed in an ICU, those who have residual symptoms detected during the teleconsultation.

Teleconsulting physicians will subject patients to a standardized questionnaire that will look for the following symptoms:

  • General signs: Anorexia, fatigue, new hospitalization, weight loss,
  • Respiratory signs: recent dyspnoea, chest discomfort, chest pain, new cough, abnormal lung CT scan since discharge
  • Neurological signs: headache, paraesthesia, anosmia, limb paralysis
  • Digestive signs: abdominal pain, diarrhoea, constipation, nausea, vomiting

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.

  • General clinical examination
  • Assessment of the state of health
  • Respiratory assessment
  • Pulmonary CT assessment
  • Cognitive evaluation
  • Cardiological evaluation
  • Renal assessment
  • Immunological evaluation

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

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Tai PHAM, Bicetre Hospital

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2021년 5월 5일

기본 완료 (예상)

2022년 5월 5일

연구 완료 (예상)

2022년 5월 5일

연구 등록 날짜

최초 제출

2021년 6월 18일

QC 기준을 충족하는 최초 제출

2021년 6월 18일

처음 게시됨 (실제)

2021년 6월 22일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 6월 22일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 6월 18일

마지막으로 확인됨

2021년 6월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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. .

구독하다