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Brown adipose tissue activity in lung cancer

Brown adipose tissue activity in lung cancer - Brown adipose tissue activity in lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37755
Enrollment
13
Registered
2012-07-25
Start date
2012-06-01
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wasting Weight loss

Interventions

None listed

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Resectable non-small cell lung cancer (NSCLC) Age 40-70 years Gender: male and female Caucasians Non-obese persons, i.e. Body Mass Index (BMI)

Exclusion criteria

Exclusion criteria: Primary • Body Mass Index > 30 kg/m2 • Medically treated Diabetes mellitus (oral anti-diabetics, insulin) • Severe COPD and/or heart failure • Patients with severe clotting disorder • Patients with a second malignancy, either active or in previous medical history • Thyroid disorders • Psychological unstable persons presumed unfit to perform the measurements, including claustrophobia • Patients with shortness of breath in rest • Persons unable to lie or sit still for1-2 hours • Pregnant subjects • Subjects that received high doses of radiotherapeutic radiation of the neck and/or upper chest in their medical history • Persons that received cervical of thoracic sympathectomy or have a nerve dysfunction which is likely to influence sympathetic nerves • The use of the medication that influences the sympathetic nerve system: ß-blockers, a-blockers, central anti-hypertensives, certain anti-depression drugs (MAO inhibitors, tricyclic anti-depressives) reserpine, cocaïne, calciumblockers, labetalol, certain tranquillizers (fenothiazines) • Exclusion criteria for core temperature measurement: -In any patient whose body weight is less than 40 kg -In the presence of any known or suspected obstructive disease of the gastrointestinal tract -In any patient exhibiting or having a history of disorders or impairment of the gag reflex -In any patient with previous gastrointestinal surgery -In any patient having structural and/or functional disorders of the esophagus -In any patient who might undergo Nuclear Magnetic Resonance (NMR) or MRI scanning during the period that the CorTemp* Disposable Temperature Sensor is within the body. -In any patient with hypo motility disorders of the gastrointestinal tract -In any patient having a cardiac pacemaker or other implanted electro medical device.;Secondary • Unsuccesful complete macro- and microscopic resection of the lung tumor • Presence of tumor recurrence on the second PET-CT scan

Design outcomes

Primary

MeasureTime frame
BAT volume and intensity in kBq/SUV in the presence (before operation) compared to absense (after operation) of lung cancer, as determined by 18 F-FDG PET-CT scanning.

Secondary

MeasureTime frame
Second primary endpoint are the effects on energy expenditure, body core temperature, skin surface temperature, body composition and serum leverls of CRP and selected hormones that influence BAT activity

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)