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Covid19NCT05200819

Incidence and Predictors of Acute and Chronic Complications in Patients With Diabetes and Severe COVID-19

An observational study of Covid19 and Diabetes Mellitus, run by University of Michigan at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

All surviving patients of the Michigan Medicine COVID-19 Cohort (M2C2, PI: Hayek) that were admitted to the University of Michigan for severe COVID-19 disease are eligible for this study. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Covid19, Diabetes Mellitus
How many people
70 participants
Where
1 siteUnited States
Study dates
2 Dec 2020to 20 Feb 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Living patients who were hospitalized for COVID-19 infection (Michigan Medicine COVID-19 or M2C2 Cohort) will be invited to participate in this study. In addition, any patient who has survived COVID-19 infection (regardless of whether they were hospitalized) may be enrolled.

Who may be able to join

None listed.

Who cannot join

  • Women who are currently pregnant or breastfeeding

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Michigan

    Ann Arbor, Michigan, 48105

Other trials in United States

About this study

All surviving patients of the Michigan Medicine COVID-19 Cohort (M2C2, PI: Hayek) that were admitted to the University of Michigan for severe COVID-19 disease are eligible for this study. Investigators had prior approval from the Institutional Review Board (IRB) to collect the baseline blood and urine samples of these participants. Initial analysis on those samples are ongoing. In preliminary analysis of these patients a significantly higher risk for severe acute complications in patients with diabetes compared to those without diabetes was observed. The study will also enroll people following documented COVID-19 infection, regardless of whether or not they were hospitalized. The goal of the study is to understand what drives the increased risk of severe acute COVID-19 complications as well as to understand the long term sequelae of COVID-19 infection in patients with diabetes. The objectives of this study are to invite surviving M2C2 participants as well as others who have survived COVID-19 infection for an in-person visit, to measure biomarkers of inflammation and kidney, nerves, heart and blood vessels damage. participants will also be comprehensively phenotyped for diabetic complications outcomes, diabetes kidney disease, diabetes neuropathy and cardiovascular disease. Participants will be asked to fill out questionnaires to assess psychosocial metrics. The rationale is that correlating markers of acute hyperinflammation (cytokine storm syndrome) at admission in diabetes patients can inform vigilance and care for long term complications in survivors. Completing these studies will generate evidence-based guidelines for mitigating sequelae in diabetes COVID-19 survivors and identify critical psychosocial factors to mitigate psychological harm.

Read the detailed description

Diabetic patients, particularly those with type 2 diabetes (T2D), are highly susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induced adverse outcomes and complications. The massive global T2D burden and high COVID-19 infection rate is creating large and significantly vulnerable COVID-19 T2D patient populations.

The prevalence of diabetes among admitted COVID-19 infections has varied 20-50% by region.T2D patients are more prone to a severe COVID-19 disease course, marked by dangerous infection-induced adverse outcomes and complications including intensive care unit (ICU) admission, mechanical ventilation use, or death. The clinical experience with patients admitted to the Michigan Medicine COVID-19 Cohort (M2C2, PI: Hayek): 42% of COVID-19 cases had diabetes, and a disproportionally larger fraction, 56%, required ICU admittance and suffered over twice the mortality (22%) compared to non-diabetic (10%) patients. Thus, T2D consistently predisposes COVID-19 patients to poorer prospects, including acute kidney injury, cardiovascular complications and death.

Most T2D patients frequently suffer from comorbidities, including metabolic syndrome (obesity, hypertension), chronic inflammation, and vascular diabetic complications, i.e., diabetic kidney disease (DKD), diabetic neuropathy (DN), and cardiovascular disease (CVD). In the multi-center French Coronavirus SARS-CoV-2 and Diabetes Outcomes (CORONADO) study (n=1,317 diabetic participants, 88.5% T2D), obesity, measured by body mass index (BMI) positively predicted the study primary outcome, tracheal intubation for mechanical ventilation and/or death within 7 days of admission. The presence of micro- and macrovascular complications at admission independently associated with 7-day mortality, as did inflammation [C-reactive protein (CRP)]and liver injury at admission. Thus, T2D patients, through their comorbid conditions, are at an especially dangerous risk of serious COVID-19 infection and death.

The underlying reasons for the T2D patient susceptibility to COVID-19 remains unclear, although there are several theories. One is that COVID-19-induced cytokine storm syndrome (CSS) may superimpose on the chronic inflammation already present in T2D, promoting a vicious cycle of cytokine release and hyperglycemic surges. T2D is characterized by a chronic, low-grade inflammation, which is also a feature of its complications, DKD, DN, and CVD. Importantly, there are no studies stratifying patients by diabetes status to determine whether a biomarker would be especially useful for predicting the clinical course in COVID-19 T2D patients.

It is also becoming clear that COVID-19 survivors may face a lifetime of sequelae. As with acute infection, T2D patients may also be particularly at risk here. Although the pandemic has not yet lasted long enough to measure long term outcomes, the evidence to date suggests a significant burden of new complications. For instance, COVID-19 may aggravate preexisting pathology, including in T2D patients, and multi-organ injury that aggravates tissues already weakened by preexisting diabetic complications. Finally, the COVID-19 pandemic has seen racial health disparities soar. SARS outbreak survivors report long term effects, even years later, including psychological and financial hardship. In addition, given the disparity during the COVID-19 pandemic, racial minorities faced even more hardships. Identifying these psychosocial factors could mitigate long term psychological trauma. The challenges of the long-term consequences of COVID-19 are emerging as a growing number of patients are long-term survivor sequelae. Identifying these COVID-19 patients who experienced serious clinical complications during their inpatient hospitalization and then sequelae after the acute phase, will deliver better long term outpatient care and allow to preemptively screen for new onset and progression in all complications.

Keywords
Covid19, Diabetes Mellitus
Medical subject headings
COVID-19, Diabetes Mellitus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05200819
Study groupRoleWhat they receive
COVID 19 PatientsPatients who have survived COVID-19 infection, including those included in the Michigan Medicine COVID-19 Cohort (M2C2) will be eligible to participate.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Risk-marker signatures for severe COVID-19 disease, longer-term complications in patients surviving COVID-19.

    Comprehensively phenotype COVID-19 survivors for vascular outcomes including kidney disease, peripheral and autonomic neuropathy, cardiovascular disease, as well as cognitive disorders and and patient-reported outcomes.

    Measured: Single visit lasting 2 to 6 hours. Visit will occur within 3 years of COVID-19 diagnosis

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jan 2022
  2. Study start2 Dec 2020
  3. Primary completion20 Feb 2023
  4. Study completion20 Feb 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05200819
Sponsor's protocol ID
HUM00186076
Status last verified
Dec 2023
First submitted
17 Jan 2022
Last updated
13 Dec 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Covid19 and Diabetes Mellitus, run by University of Michigan at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Risk-marker signatures for severe COVID-19 disease, longer-term complications in patients surviving COVID-19. (time frame: Single visit lasting 2 to 6 hours. Visit will occur within 3 years of COVID-19 diagnosis). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Dec 2023.

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