Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New Radiation-Free imaging could shed light on brown Fat's role in metabolic health

NCT ID NCT07327684

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study is testing a new, safe imaging technique called photoacoustic imaging to look at brown adipose tissue (BAT), a type of body fat that burns energy. Researchers will compare BAT in healthy adults and people with metabolic syndrome to see if the imaging can spot differences. The goal is to create a simple tool to help diagnose and track metabolic conditions without radiation.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 100 people

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

Started

May 2025

Expected to finish

Dec 2027

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.

Ages

18 to 80 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.

Criteria for Healthy Subjects: (INCLUSION CRITERIA) 1. Healthy individuals over 18 years of age. 2. Body Mass Index (BMI) \< 30. 3. No history of metabolic diseases, rheumatic immune diseases, or cardiovascular and cerebrovascular diseases. 4. Not currently using any sympathomimetic or sympatholytic drugs. 5. Non-smoker and does not consume excessive alcohol. (EXCLUSION CRITERIA) 1. Weight change \> 5% within 3 months prior to enrollment. 2. BMI ≥ 30. 3. Diagnosis of metabolic disease, rheumatic immune disease, cardiovascular and cerebrovascular disease, or malignant tumor. 4. Use of sympathomimetic or sympatholytic drugs within 3 months prior to enrollment. 5. Smoker or consumes excessive alcohol. 6. Diagnosis of Raynaud's disease, or intolerance/allergy to cold stimulation. 7. Currently pregnant, lactating, or menstruating. 8. Contraindications to the injection of the radionuclide tracer Fluorodeoxyglucose (18F-FDG) or other conditions unsuitable for PET-CT examination. Criteria for Patients with Metabolic Syndrome and Insulin Resistance-Related Diseases: (INCLUSION CRITERIA) 1. Age between 18 and 60 years. 2. Must meet 3 or more of the following criteria: 1. Waist circumference ≥ 90 cm for males, ≥ 85 cm for females. 2. Fasting blood glucose ≥ 6.10 mmol/L (110 mg/dl) OR 2-hour postprandial blood glucose ≥ 7.80 mmol/L (140 mg/dl) OR previously diagnosed diabetes. 3. Blood pressure ≥ 130/85 mmHg OR previously diagnosed hypertension and under treatment. 4. Fasting triglycerides (TG) ≥ 1.7 mmol/L (150 mg/dl). 5. Fasting high-density lipoprotein cholesterol (HDL-C) \< 1.0 mmol/L (40 mg/dl). 3. Patients diagnosed with Polycystic Ovary Syndrome (PCOS), defined as meeting two or more of the following criteria and excluding other endocrine diseases that could cause similar symptoms: hyperandrogenism, ovulatory dysfunction, polycystic ovary morphology. (EXCLUSION CRITERIA) 1. Diagnosis of Type 1 diabetes or other specific types of diabetes. 2. Presence of acute diabetic complications or severe chronic diabetic complications. 3. History of acute or chronic pancreatitis, or pancreatic tumors. 4. Heart failure, unstable angina, myocardial infarction within the past 12 months, cerebral infarction, severe arrhythmia, or severe hypertension (blood pressure \> 180/110 mmHg despite antihypertensive medication). 5. Severe hepatic or renal dysfunction. 6. Comorbid malignant tumors or other severe chronic diseases. 7. Received glucose-lowering therapy within 3 months prior to enrollment OR a total of more than 3 months of glucose-lowering therapy in the past 2 years. 8. Diagnosis of rheumatic immune diseases. 9. Diagnosis of Raynaud's disease, or intolerance/allergy to cold stimulation. 10. Currently pregnant, lactating, or menstruating. 11. Contraindications to the injection of the radionuclide tracer Fluorodeoxyglucose (18F-FDG) or other conditions unsuitable for PET-CT examination.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Insulin resistance are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

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

  • Peking Union Medical College Hospital

    RECRUITING

    Beijing, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.