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NCT05985135Withdrawn

Impact of Insulin Deprivation and Hyperglycemia on Plasma Protein Synthesis in People With Type 1 Diabetes Mellitus

Impact of Insulin Deprivation and Hyperglycemia on Plasma Protein Synthesis in People With Type 1 Diabetes Mellitus and Diabetes After Total Pancreatectomy

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

This research is being done to better understand how insulin effects muscle, blood, and the body in people with Type 1 Diabetes.

Status (registry)
Withdrawn
Study type
Interventional
Enrollment
0 (actual)
First submitted
2 Aug 2023
Start date
1 Jun 2026
Primary completion date
31 Jul 2026
Lead sponsor
Mayo Clinic
NCT number
NCT05985135

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Celiac disease.
  • Reported history of illicit substance use.
  • History of active cardiovascular, cerebrovascular, or peripheral vascular disease.
  • Dementia or any other neurologic disease.
  • Uncontrolled psychiatric disease.
  • Celiac disease.
  • Reported history of illicit substance use.
  • History of active cardiovascular, cerebrovascular, or peripheral vascular disease.
  • Dementia or any other neurologic disease.
  • Uncontrolled psychiatric disease.

Lab values

  • Active renal disease evidenced by estimated glomerular filtration rate (GFR) < 50 mL/min/1.73 m\^2.
  • Hemoglobin A1c > 9.0%.
  • Type 2 Diabetes Mellitus (T2DM), or impaired fasting glucose.
  • Active renal disease evidenced by estimated GFR < 50 mL/min/1.73 m\^2.
  • T2DM, or impaired fasting glucose.

Other

  • BMI < 20 or > 32 kg/m\^2.
  • Pregnancy.
  • Smoking.
  • Severe peripheral or autonomic neuropathy.
  • Any learning disability.
  • Anemia.
  • Thyroid-stimulating hormone (TSH) ≥ 7 or TSH ≤ 7 and free T4 ≤ 0.9.
  • Detectable C peptide.
  • BMI < 20 or > 32 kg/m\^2.
  • Pregnancy.
  • Smoking.
  • Severe peripheral or autonomic neuropathy.
  • Any learning disability.
  • Anemia.
  • TSH ≥ 7 or TSH ≤ 7 and free T4 ≤ 0.9.

Who the study is looking for

  • Able to provide written consent.
  • Able to provide written consent.
  • T1DM treated with continuous subcutaneous insulin infusion (CSII) or multiple daily injections (MDI) (not Degludec).

Age in the registry: 18 years to 70 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.