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Targeting the Carotid Bodies to Reduce Disease Risk Along the Diabetes Continuum

University of Missouri (MU) logo

University of Missouri (MU)

Status

Completed

Conditions

Type 2 Diabetes

Treatments

Other: Normoxia Exposure
Other: Hyperoxia Exposure

Study type

Interventional

Funder types

Other

Identifiers

NCT05219994
2018486

Details and patient eligibility

About

Our overall goal is to advance our understanding of the contribution of the carotid body chemoreceptors in glucose regulation and the development of type 2 diabetes.

Enrollment

22 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy,
  • type 2 diabetes
  • BMI 18-40 kg/m2,
  • non-pregnant,
  • non-breastfeeding,
  • non-nicotine users.

Exclusion criteria

  • cardiovascular disease including myocardial infarction, heart failure, coronary artery disease, stroke;
  • renal or hepatic diseases;
  • active cancer;
  • autoimmune diseases;
  • immunosuppressant therapy;
  • excessive alcohol consumption (>14 drinks/week);
  • current nicotine use;
  • foot ulcers;
  • diabetic neuropathy;
  • medication directly influencing sympathetic nervous system activity

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

22 participants in 1 patient group

Oral Glucose Tolerance Test
Experimental group
Description:
Subjects will consume a 75 g glucose drink within 1-min and monitored for 2 hours.
Treatment:
Other: Hyperoxia Exposure
Other: Normoxia Exposure

Trial contacts and locations

1

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Central trial contact

Jennifer L Harper, B.S.

Data sourced from clinicaltrials.gov

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