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Scientists hunt for hidden signals in muscle cells that could explain insulin resistance

NCT ID NCT07516509

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times

Summary

This study aims to find new signs in muscle cells that help explain why the body stops responding well to insulin, a condition called insulin resistance. Researchers will study 36 adults aged 30 to 65, including lean individuals and those with obesity, using advanced cell analysis and fitness tests. The goal is to better understand the biology behind insulin resistance, not to test a new drug or treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could reveal new biological markers for insulin resistance, potentially guiding future treatments.
What could go wrong
This is an early observational study with only 36 participants, so findings may not apply broadly. It does not test a treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 36 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The investigators are studying sedentary men and women between the ages of 30 and 65 years with; either a body mass index (BMI) between 18-25 kg/m2 or 30-40 kg/m2.

Ages

30 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * All Groups 1. 30 to 65 years of age 2. Stable weight (No Gain/Loss of \>10 lbs in 6 months) 3. Sedentary (≤ 1 continuous exercise/week) 4. Non-smoker 5. Resting Blood Pressure ≤ 150mmHg systolic and ≤ 95 mmHg diastolic Group A - Lean individuals with insulin sensitivity (IS-Lean) 1. BMI 18-25 kg/m2 2. Hemoglobin A1c ≤ 5.6% at screening 3. Blood glucose level ≤ 140 mg/dL 2hr after a 75g oral glucose tolerance test Group B - Individuals with obesity and insulin sensitivity (IS-Obesity) 1. BMI 30-40 kg/m2 2. Hemoglobin A1c ≤ 5.6% at screening 3. Blood glucose level ≤ 140 mg/dL 2hr after a 75g oral glucose tolerance test Group C - Individuals with obesity and insulin resistance (IR-Obesity) 1. BMI 30-40 kg/m2 2. Hemoglobin A1c ≤ 6.4 % at screening 3. Blood glucose level 140-199 mg/dL 2hr after a 75g oral glucose tolerance test Exclusion Criteria: 1. Clinically significant CVD including h/o MI, within the past year 2. Peripheral Vascular Disease 3. Diagnosed with Type I or Type II diabetes 4. Hepatic, renal, muscular/neuromuscular, or active hematologic/oncologic disease 5. Previous history of pulmonary emboli 6. Peripheral Neuropathy 7. Anemia (Hematocrit \<34%, Hemoglobin \< 14 gm/dL for men and \<12.3 gm/dL for women) at screening 8. Currently pregnant (pregnancy test performed on day of DEXA scan in women of child-bearing potential); post-partum during the last 12 months; lactating during the last 12 months; planning to become pregnant during the participation period 9. Polycystic Ovarian Syndrome (PCOS) (self-report) 10. Hospitalization for COVID-19 infection in the past 12 months; individuals who tested positive for COVID-19 but were not hospitalized must be symptom-free at least 14 days 11. Partial and/or full hysterectomy (self-report) 12. Not willing to archive biospecimens for future use 13. Any contraindications to exercise testing according to ACSM guidelines 14. Inability and/ or unwillingness to comply with the protocol as written 15. Active alcohol or substance abuse (Past 5 Years) 16. Positive toxicology result from screening visit or chronic use of Amphetamine, Barbiturate, Benzodiazepine, Cocaine, Methadone, Opiate, THC, Cannabis, Tricyclics, or Oxycodone. 17. Dyslipidemia (fasting triglycerides \>500 mg/dL; low-density lipoprotein cholesterol (LDL-C) \>190 mg/dL; total cholesterol \>300 mg/dL); 18. ALT \>80, AST\>80, Alk Phos \>240 if a participant presents with liver functions out of these ranges at screening the MI or PI can give discretion to participate 19. Proteinuria (defined as \> 1+) at screening 20. Kidney disease (creatinine \>1.6 mg/dl or estimated glomerular filtration rate \<60 mL/min/1.73m2); 21. Self-reported chronic, active, or latent infection requiring chronic antibiotic or anti-viral treatment; Human Immunodeficiency Virus (HIV); active hepatitis B or C undergoing antiviral therapy. 22. Receiving active treatment (including monoclonal antibodies) for autoimmune disorders within the last 6 months; 23. Hypothyroidism (sTSH\>8) at screening or on thyroid replacement therapy 24. Abnormal bleeding or coagulopathy (self-report) or history of a bleeding disorder or clotting abnormality 25. History of cancer (other than non-melanoma skin cancer) within the last 5 years (not in remission); anti-hormonal therapy (e.g., for breast or prostate cancer) within the last 6 months; 26. Previous bariatric or other surgery for obesity 27. Females currently on hormone replacement therapy (HRT) less than 6 months 28. Females with an irregular menstrual cycle 29. Previous difficulty with lidocaine or other local anesthetic 30. ACS symptoms: * Positive ECG (\> 2mm ST segment depression) without PCP cardiologist permission to participate * Signs or symptoms of cardiovascular decomposition (eg. hypotensive response to exercise) * Onset of angina or angina like symptoms, shortness of breath, change in heart rhythm, signs of poor perfusion (light-headedness), tightness. 31. The following medication use is exclusionary; * Dose change for any chronic-use drug in the last 3 months; * Any medications that can alter glucose homeostasis (eg. steroids, glucocorticoids, nicotinic acid). Acute therapy (5-7 days) is not exclusionary however; participant must be agreeable to a washout period of 5-7 days prior to day of biopsy. * Blood thinners such as Coumadin, Lovenox etc. Aspirin is not exclusionary however; participant must be agreeable to a washout period of \> 10 days prior to day of biopsy * All Weight loss medications including but not limited toGLP-1 agonists- Wegovy, liraglutide, semaglutide, Trulicity (dulaglutide), Phentermine and Contrave * Cardiovascular: beta blockers and centrally acting anti-hypertensive drugs, anticoagulants, antiarrhythmics, and antiplatelet drugs (other than aspirin ≤100 mg/day); * Psychiatric: chronic use of medium- or long-acting sedatives and hypnotics, including all benzodiazepines (short-acting non-benzodiazepine sedative-hypnotics are allowed), mood stabilizers, antiepileptic drugs, stimulants, Attention-Deficit/Hyperactivity Disorder (ADHD) drugs, anti-psychotic drugs, anti-depressant medication (e.g. Bupropion, selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine re-uptake inhibitors (SNRIs)). * Pulmonary/Inflammation: chronic oral steroids (occasional use of inhaled steroids are allowed), burst/taper oral steroids more than once in the last 12 months, B2-agonists (allowed if on stable dose at least 3 months). * Genitourinary: 5-alpha reductase inhibitors, daily use of phosphodiesterase type 5 inhibitor. * Hormonal: androgenic anabolic steroids, anti-estrogens, anti-androgens, estrogens and/or progestins used for reasons other than birth control, growth hormone, insulin like growth factor-I, growth hormone releasing hormone, * any drugs used to treat diabetes mellitus or lower blood glucose including metformin, thiazolidinediones, SGLT-2 inhibits or insulin * any drugs used specifically to induce muscle growth/hypertrophy or augment exercise-induced muscle hypertrophy * Pain/Inflammation: narcotics and narcotic receptor agonists, regular use of non-steroidal anti-inflammatory drugs (NSAIDs) or acetaminophen, muscle relaxants ≥2 days per week * Other: chronic systemic antimicrobials (antibiotic, antiviral, antifungal, antiparasite, etc.) for any reason, high-potency topical steroids if ≥10% surface area using rule of 9s, continuous/chronic use of antibiotics or other anti-infectives for treatment or prevention, monoclonal antibodies, anti-rejection medications/immune suppressants. Participants can be re-screened after a 3 month washout period if antimicrobial use is only used acutely \< 2 weeks. 32. Presence of any condition that, in the opinion of the Investigator, compromises participant safety or data integrity or the participant's ability to complete the study.

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Conditions

The condition(s) this trial relates to.

Insulin Resistance

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • AdventHealth Translational Research Institute

    RECRUITING

    Orlando, Florida, 32804, United States

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