PHENOTYPE: PHenotyping patiENts Admitted to Hospital With cOvid-19 Infection and idenTifYing Prognostic markErs

Sponsor
Chelsea and Westminster NHS Foundation Trust (Other)
Overall Status
Recruiting
CT.gov ID
NCT04459351
Collaborator
(none)
500
1
35.4
14.1

Study Details

Study Description

Brief Summary

PHENOTYPE is an investigator-led, observational cohort study which aims to explore the long-term outcomes of patients with COVID-19 infection and to identify potential risk factors and biomarkers that can prognosticate disease severity and trajectory.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    In 2019, a novel coronavirus, SARS-CoV-2 was first identified in Wuhan, China. SARS-CoV-2 infection, denominated COVID-19, causes a predominantly respiratory illness, which varies from mild respiratory symptoms to multi-organ failure and death. In March 2020, COVID-19 was designated pandemic status and as of May 2020 there have been more than 3.7 million cases reported worldwide and 257,000 deaths attributed. In the UK, COVID-19 has caused more than 30,000 deaths to date.

    Although respiratory symptoms are the commonest presentation, numerous systemic complications of COVID-19 have been identified, including those affecting the cardiovascular, neurological, gastroenterological, and renal systems. The long-term impact of these complications on survivors and the risk factors for long term sequelae is not presently known. It is likely that increased frailty and psychological sequelae will be significant, which could lead to a persistent reduction in quality of life, as observed in the previous SARS pandemic.

    This cohort study aims to evaluate the respiratory, cardiac, renal and psychological outcomes of patients diagnosed with COVID-19 infection and determine the pathophysiological mechanisms that contribute to disease severity and disease burden.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Other
    Official Title:
    PHenotyping patiENts Admitted to Hospital With cOvid-19 Infection and idenTifYing Prognostic markErs
    Actual Study Start Date :
    Jun 19, 2020
    Anticipated Primary Completion Date :
    May 1, 2023
    Anticipated Study Completion Date :
    Jun 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Identification of baseline characteristics which correlate with disease severity [Based on clinical need - Up to 1 year follow up.]

      The primary purpose is to characterise the different presentations and features of COVID-19 and outcomes.

    2. Identification of blood biomarkers which correlate with disease severity [Based on clinical need - Up to 1 year follow up.]

      Relationship between changes in markers of inflammation (CRP, D dimer, ferritin, fibrinogen, pro-calcitonin) and pulmonary, renal and cardiac complications post hospitalisation for Covid-19 infection.

    3. Genomic analysis of blood samples to look for genetic susceptibility to severe disease presentations [Based on clinical need - Up to 1 year follow up.]

      Genomic, proteomic and transcriptomic analysis of blood samples to look for genetic susceptibility to severe disease presentations and to identify new biomarkers that predict disease severity or disease trajectory

    Secondary Outcome Measures

    1. Incidence [Based on clinical need - Up to 1 year follow up.]

      Incidence of: Interstitial lung disease Pulmonary embolism Pulmonary hypertension as determined by pulmonary artery systolic pressure on echocardiogram or mean pulmonary artery pressure on right heart catheterisation if performed Renal dysfunction (as defined by new persistent impairment of egfr or new sustained protenuria measured using urinary protein-creatinine ratio) Cardiac dysfunction (new LV or RV systolic dysfunction on echocardiogram) Psychological distress as measured using Hospital anxiety and depression scale

    2. Change in respiratory symptom scores [Based on clinical need - Up to 1 year follow up.]

      Assessed through Leicester Cough Questionnaire: Domain scores 1-7; Total scores 3-21

    3. Change in respiratory symptom scores [Based on clinical need - Up to 1 year follow up.]

      Assessed through the modified Medical Research Council Dyspnoea Scale: Scores range from 0-4.

    4. Change in frailty and quality of life scores [Based on clinical need - Up to 1 year follow up.]

      Assessed thought the Short Form Survey (36): 8 scales, each scored between 0-100.

    5. Change in frailty and quality of life scores [Based on clinical need - Up to 1 year follow up.]

      Assessed through the Clinical Frailty Scale: Scores range from 1-9.

    6. Relationship between serum markers and clinical outcomes [Based on clinical need - Up to 1 year follow up.]

      D dimer/ fibrinogen and new pulmonary embolism

    7. Relationship between serum markers and clinical outcomes [Based on clinical need - Up to 1 year follow up.]

      Troponin/ BNP and cardiac disease

    8. Relationship between serum markers and clinical outcomes [Based on clinical need - Up to 1 year follow up.]

      Markers of inflammation (CRP, procalcitonin, ferritin, fibrinogen, D dimer, ESR) and persistent radiological abnormalities

    Other Outcome Measures

    1. Thematic analysis of semi-structured interviews exploring the following areas: [Up to 1 year follow up.]

      Changes in health behaviours such as alcohol consumption and tobacco use Mental health and psychological wellbeing Factors affecting compliance with Public Health England guidelines The impact of cultural and religious beliefs on behaviours during the pandemic

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria

    • Aged 18 years or older

    • Confirmed COVID-19 infection (as per national guidelines)

    • Attending follow-up outpatient visit post hospital attendance with COVID-19 infection

    Exclusion Criteria

    There are no specific exclusion criteria

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chelsea and Westminster Hospital London United Kingdom SW10 9NH

    Sponsors and Collaborators

    • Chelsea and Westminster NHS Foundation Trust

    Investigators

    • Principal Investigator: Pallav Shah, MBBS, MD, Chelsea and Westminster Hospital NHS Foundation Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Chelsea and Westminster NHS Foundation Trust
    ClinicalTrials.gov Identifier:
    NCT04459351
    Other Study ID Numbers:
    • C&W20/035
    First Posted:
    Jul 7, 2020
    Last Update Posted:
    Aug 9, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Chelsea and Westminster NHS Foundation Trust
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 9, 2021