CClinicalTrials.gg
WithdrawnNCT05985135Updated Aug 5, 2026

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

An interventional study of Muscle Biopsy and Jell-O with Amino acids in Type 1 Diabetes, sponsored by Mayo Clinic. Withdrawn at 1 site in United States. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-05.

Sponsored by Mayo Clinic · Not applicable, Interventional, and Health services research

Why this study was withdrawn
Changed IRB number
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

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

Read the detailed description

Insulin's contribution in controlling glucose homeostasis has been well appreciated but, its role in maintaining proteome homeostasis is less understood. Some animal and human studies have demonstrated that insulin signaling regulates protein synthesis and degradation as well as posttranslational modifications at the tissue level. Insulin's effect on the muscle's mitochondrial proteo-stasis has also been elucidated. Insulin deprivation increases global synthesis of splanchnic proteins based on isotope dilution studies across splanchnic bed. Most plasma proteins are derived from liver and preliminary studies suggest that synthesis rates of some plasma proteins increase while others decrease. Fractional rates of synthesis of various plasma proteins from the liver have been demonstrated in insulin deprivation state. These proteins might be implicated in the development of some of the complications from diabetes mellitus type 1. (T1DM) especially of macrovascular. Researchers have recently developed an isotope-based methodology to simultaneously measure in vivo synthesis rates of multiple plasma proteins in human.

In order to further investigate the effects of insulin deprivation researchers will apply the novel non-radioactive stable isotope-based approach on the rate of different plasma protein synthesis in T1DM and Diabetes after total pancreatectomy (DATP) in comparison with non-diabetic controls. Researchers will study pancreatectomized people because like T1DM they also are insulin deficient but unlike pancreatectomized people also are deficient in glucagon. Some tantalizing data from many studies indicate that glucagon also have catabolic effect not only on liver derived proteins but also on skeletal muscle-based proteins. Since skeletal muscle has no glucagon receptors, researchers hypothesize that unknown factors are released to the circulation that act on skeletal muscle to release amino acids for consumption in liver. Researchers will measure amino metabolites, acyl carnitines, organic acids, and ceramides in plasma and determine the blood exosome cargo by mass spectrometry-proteins and lipids and miRNA by PCR.

Researchers have previously shown reduced muscle mitochondrial ATP production during insulin deprivation in both T1D humans and diabetic mice and here researchers will measure mitochondrial energy dynamics in all study participants by the established techniques available in our lab.

02

Conditions studied

  • Type 1 Diabetes

Keywords

  • Continuous subcutaneous insulin infusion
  • Multiple daily injections of insulin
03

In context

Diabetes Mellitus, Type 1

3,522 studies on the registry are indexed under Diabetes Mellitus, Type 1; 577 are open to participants now.

Browse Diabetes Mellitus, Type 1 studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 669 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria - Type 1 Diabetes Group:

- Able to provide written consent.

Exclusion Criteria - Type 1 Diabetes Group::

  • BMI \< 20 or > 32 kg/m\^2.
  • Celiac disease.
  • Pregnancy.
  • Smoking.
  • Reported history of illicit substance use.
  • History of active cardiovascular, cerebrovascular, or peripheral vascular disease.
  • Active renal disease evidenced by estimated glomerular filtration rate (GFR) \< 50 mL/min/1.73 m\^2.
  • Severe peripheral or autonomic neuropathy.
  • Dementia or any other neurologic disease.
  • Uncontrolled psychiatric disease.
  • Any learning disability.
  • Anemia.
  • Thyroid-stimulating hormone (TSH) ≥ 7 or TSH ≤ 7 and free T4 ≤ 0.9.
  • Hemoglobin A1c > 9.0%.
  • Type 2 Diabetes Mellitus (T2DM), or impaired fasting glucose.
  • Detectable C peptide.

Inclusion Criteria - Control Group:

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

Exclusion Criteria - Control Group:

  • BMI \< 20 or > 32 kg/m\^2.
  • Celiac disease.
  • Pregnancy.
  • Smoking.
  • Reported history of illicit substance use.
  • History of active cardiovascular, cerebrovascular, or peripheral vascular disease.
  • Active renal disease evidenced by estimated GFR \< 50 mL/min/1.73 m\^2.
  • Severe peripheral or autonomic neuropathy.
  • Dementia or any other neurologic disease.
  • Uncontrolled psychiatric disease.
  • Any learning disability.
  • Anemia.
  • TSH ≥ 7 or TSH ≤ 7 and free T4 ≤ 0.9.
  • T2DM, or impaired fasting glucose.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Type 1 Diabetes Mellitus (T1DM) Insulin Deprived

    Subjects will have their insulin infusions replaced with saline and have blood draws to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids

  • Experimental
    Type 1 Diabetes Mellitus (T1DM) Insulin Treated

    Subjects will continue their baseline insulin infusion while maintaining a target blood glucose range. Blood draws will be obtained to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids

  • Experimental
    Type 1 Diabetes Mellitus (T1DM) Insulin-Treated with Hyperglycemia

    Subjects will be continue their baseline insulin infusion for 2 hours and then receive an intravenous dextrose infusion to maintain elevated blood sugar levels. Blood draws will be obtained to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids · Dietary Supplement: Dextrose

  • Other
    Non-Diabetic Controls

    Subjects will have blood draws to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids

  • Experimental
    Diabetes after Total Pancreatectomized (DATP) Insulin Treated

    Subjects will continue their baseline insulin infusion while maintaining a target blood glucose range. Blood draws will be obtained to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids

  • Experimental
    Diabetes after Total Pancreatectomized (DATP) Insulin Deprived

    Subjects will have their insulin infusions replaced with saline and have blood draws to monitor glucose levels along with a muscle biopsy following consumption of a Jell-O with Amino acids.

    Procedure: Muscle Biopsy · Other: Jell-O with Amino acids

Interventions

  • ProcedureMuscle Biopsy

    Needle muscle biopsy of the outer thigh muscle

  • OtherJell-O with Amino acids

    An amino acid mixture containing 13C6 Lysine isotope label

  • Dietary supplementDextrose

    Intravenous form of sugar

06

What researchers measure

Primary outcomes

  1. Protein synthesis

    Measurement of isotope abundance in peptides derived from the digested proteins

    Time frame: Approximately 7 hours

07

Study locations

1 site
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05985135
Lead sponsor
Mayo Clinic
Responsible party
K. Sreekumaran Nair (Principal Investigator, Mayo Clinic) — Principal investigator
First posted
Aug 14, 2023
Start date
Jun 1, 2026 (estimated)
Primary completion
Jul 31, 2026
Completion
Jul 31, 2026
Last update
Aug 5, 2026

Study contacts

K. Sreekumaran Nair, MD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is withdrawn, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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