CClinicalTrials.gg
TerminatedNCT00962234Updated Feb 26, 2016

Metabolism of Lipids in Advanced Cancer

An observational study in Lung Neoplasms and Cachexia, sponsored by AHS Cancer Control Alberta. Terminated at 1 site in Canada. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2016-02-26.

Sponsored by AHS Cancer Control Alberta · Observational

Why this study was terminated
ethics approval not renewed by Study Group
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
12
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The causes of failing nutrition status in advanced cancer are not well known. The way fat is moved, stored, burned or changed into other compounds may be affected and will be followed in patients using a tracer and other blood tests. The investigators hypothesize that fat loss and wasting results from low essential fatty acid availability in the body. Changes may occur in the liver that limits distribution and availability of fat to the body as an energy source or for other essential functions.

Read the detailed description

Weight loss in cancer is the result of breakdown of fat (lipid) and muscle protein reserves. This research will explore how people with cancer use fat in their body through the use of tracers and measures in the blood. A stable isotope of hydrogen called 'deuterium' is used to trace the production of different fats by the liver. Other methods will determine how much and what types of fat are transported around the body. Body composition will be determined by CT scan and related to fat measures.

02

Conditions studied

  • Lung Neoplasms
  • Cachexia

Keywords

  • Lipogenesis
  • Lipolysis
  • Phospholipids
  • Body Composition
  • Nutritional Status
  • Lipid Metabolism
03

In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's enrollment of 12 is below the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

AHS Cancer Control Alberta is the lead sponsor of 182 studies on the registry; 31 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Lung cancer patients

Inclusion criteria

  • Low plasma phospholipids OR low plasma ratio of triglycerides to free fatty acids
  • Recent weight loss
  • Advanced stage lung cancer (Stage 3 or 4)

Exclusion criteria

Exclusion Criteria:

  • Having symptoms that may affect measures of fat metabolism (nausea, vomiting, problems swallowing, etc.)
  • Taking n-3 fatty acid supplements such as fish oil
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
12 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • Metabolism

    Lung cancer patients who exhibit abnormalities in lipid measures.

    Other: Blood draws · Biological: Oral administration of stable isotope (deuterium) · Procedure: Metabolic rate testing

Interventions

  • OtherBlood draws

    Up to 4 blood draws will be required, in the amount of about 10 mL each

  • BiologicalOral administration of stable isotope (deuterium)

    1 mg deuterium-labeled water/kg body water (loading dose), and 0.5 mg/kg body water diluted in 1 L of normal water (maintenance dose) to be consumed over the following 16 hours

    Also known as: C/D/N Isotopes, Deuterium Oxide, CAS No: 7789-20-0

  • ProcedureMetabolic rate testing

    Metabolic rate testing is a painless, non-invasive test that takes about 1h. A metabolic cart is used, which detects the amount of oxygen and carbon dioxide the body uses. Patients will lie down on a bed for 30 minutes with lights dimmed and soft music to help them relax. After 30 minutes, a canopy will be placed over the patient's head and shoulders for 30 minutes for the analysis of breath samples. This test will be performed only once for this study.

06

What researchers measure

Primary outcomes

  1. Rate of hepatic de novo lipogenesis

    Time frame: 9 months

Secondary outcomes

  1. Measures of fat transport and availability

    Time frame: 9 months

  2. Resting metabolic rate & fat oxidation

    Time frame: 9 months

07

Study locations

1 site
  • Cross Cancer Institute
    Edmonton, Alberta T6G 1Z2, Canada
08

References and documents

Related links

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 26, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00962234
Lead sponsor
AHS Cancer Control Alberta
Collaborators
Cross Cancer Institute
Responsible party
Sponsor
First posted
Aug 19, 2009
Start date
Oct 2009
Primary completion
Oct 2011
Completion
Oct 2011
Last update
Feb 26, 2016

Study contacts

Vera Mazurak, PhD
principal investigator · AHS Cancer Control Alberta

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion