- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04844632
COVID19 Vaccination: Clinical, Laboratory and Cellular Monitoring (SAPIENZAVAX)
Primary objective:
1. Monitor adverse events (Adverse Event Following Immunization - AEFI) in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
Secondary objectives:
- Monitor the antibody response in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
- Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
- Evaluate the dynamics of the infection and the protective efficacy of the vaccine against infection / disease by studying the incidence and titre of antibodies against Nucleoprotein (N) induced by natural infection;
- Evaluate the neutralizing capacity of sera vs. a panel of sera selected and analyzed in house and in in vitro microneutralization systems with live virus;
- To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.
Methodology:
- Administration at baseline of a questionnaire for the collection of clinical data.
- Perform a blood sample to measure antibody response in vaccinated subjects
- Administer a questionnaire to evaluate adverse events after vaccination
- Reassess the antibody response 1 month after complete vaccination and 6 and 12 months after the start of vaccination
- An antibody assay will be drawn in a subgroup before subjecting the subject to the vaccine.
- In a subgroup, the blood collected will also be collected in a heparinized tube for the study of cell-mediated immunity.
- In the event that a subject participating in the study presents during the course of the observation the positivity for the molecular research of SARS-CoV-2 RNA to the oro-nasopharyngeal swab, a new sample will be performed and sent to the Istituto Superiore di Sanità for the search for viral variants.
연구 개요
연구 유형
등록 (예상)
연락처 및 위치
연구 연락처
- 이름: Stefania Basili, MD
- 전화번호: +393393452523
- 이메일: stefania.basili@uniroma1.it
연구 장소
-
-
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Roma, 이탈리아, 00161
- 모병
- AOU Policlinico Umberto I
-
연락하다:
- Stefania Basili, MD
- 이메일: stefania.basili@uniroma1.it
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
Subjects (age> 18) booked for anti-SARS-CoV-2 vaccination at the AOU Policlinico Umberto I.
Subjects will include healthcare personnel, medical students and university staff recruited from Sapienza University of Rome and Umberto I university hospital.
설명
Inclusion Criteria:
All subjects vaccinated or to be vaccinated at the AOU Policlinico Umberto I and who will agree to join the study.
Exclusion Criteria:
All subjects who refuse to give consent or who have contraindications to vaccination.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Adverse Event Following Immunization - AEFI
기간: 12 months from immunization
|
Adverse events (Adverse Event Following Immunization - AEFI) monitoring in vaccinated subjects and analyze associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
|
12 months from immunization
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Antibody response in vaccinated subject
기간: 1, 3, 6, 12 months from immunization
|
To monitor the antibody response in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
|
1, 3, 6, 12 months from immunization
|
|
Anti-Spike immune response
기간: 1, 3, 6, 12 months from immunization
|
Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
|
1, 3, 6, 12 months from immunization
|
|
Anti- Nucleoprotein (N) induced by natural infection evaluation
기간: 1, 3, 6, 12 months from immunization
|
To assess the dynamics of the infection and the protective efficacy of the vaccine against infection / disease by studying the incidence and titre of antibodies against Nucleoprotein (N) induced by natural infection;
|
1, 3, 6, 12 months from immunization
|
|
Neutralizing capacity of sera
기간: 1, 3, 6, 12 months from immunization
|
to evaluate the neutralizing capacity of sera vs. a panel of sera selected and analyzed in house and in in vitro microneutralization systems with live virus
|
1, 3, 6, 12 months from immunization
|
|
Cell-mediated immune response
기간: Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
|
To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.
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Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
|
공동 작업자 및 조사자
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
- COVID19 vaccination_Sapienza
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. .
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