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Long-Term Sequelae of SARS-COV-2 Infection: Diabetes Mellitus

Recruiting
Conditions
COVID-19
Diabete Mellitus
Registration Number
NCT05867017
Lead Sponsor
The University of Texas Health Science Center at San Antonio
Brief Summary

Hospitalized patients with severe COVID-19 have an increased incidence of insulin resistance, impaired beta cell function, glucose intolerance (prediabetes), and overt type 2 diabetes (T2D) compared to non-hospitalized patients with COVID-19 and COVID-19 negative individuals on long-term follow up.

Detailed Description

The purpose of this research study is to understand the long-term effects of COVID-19 infection on individuals without any prior history of diabetes. This study will look at several measures of diabetes, such as glycemic control (blood glucose/sugar levels), function of beta cells (cells that make insulin to control sugar), insulin secretion and insulin sensitivity (fasting insulin levels).

The following participants will be enrolled: 1) have had COVID-19 infection and were hospitalized and recovered, or 2) have had mild COVID-19 infection and were seen at outpatient clinics or ER and were not required to be hospitalized, or 3) have not had COVID-19 infection but were seen in outpatient clinics or ER during the same time period.

The researchers hope to learn the long-term effects of COVID-19 infection in hospitalized patients. Specifically, they will be focusing on the subsequent development of diabetes and associated metabolic disturbances, such as impaired insulin secretion and insulin resistance. A relationship between COVID-19 and diabetes needs to be investigated.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
213
Inclusion Criteria
  • Body Mass index (BMI) < 40 kg/m2
Exclusion Criteria
  • History of diabetes prior to SARS-CoV-2 infection
  • Took medications used to treat diabetes prior to SARS-CoV-2 infection
  • History of myocardial infarction or stroke within 6 months
  • History of major organ system disease prior to COVID-19 infection

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measure of glycosylated glucose percentage (HbA1c)Baseline to 24 months

Change in HbA1c, and indication of glucose levels over a 3 month period

Measure of free plasma glucose (FPG)Baseline to 24 months

Change in FPG

Secondary Outcome Measures
NameTimeMethod
Body WeightBaseline to 25 months

Change in body weight over the study period

Trial Locations

Locations (1)

Texas Diabetes Institute - University Health System

🇺🇸

San Antonio, Texas, United States

Texas Diabetes Institute - University Health System
🇺🇸San Antonio, Texas, United States
Andrea Hansis-Diarte, MPh
Contact
210-567-6691
hansisdiarte@uthscsa.edu
Marzieh Salehi, MD
Contact
salehi@uthscsa.edu

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