CClinicalTrials.gg
Active, not recruitingNCT06206785REPATUpdated Jun 29, 2026

Resting Energy Expenditure in Palliative Cancer Patients

An observational study in Cancer and Cachexia, sponsored by Norwegian University of Science and Technology. Active, not recruiting at 1 site in Norway. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-29.

Sponsored by Norwegian University of Science and Technology · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
160
Ages
18 Years and older
Sex
All
01

Study summary

The study purpose is to measure REE by indirect calorimetry and to determine limits of agreement with confidence intervals between measured REE and predictive equations for determination of energy requirements in patients with incurable cancer. Clinical factors associated with hyper- and hypometabolism will be elucidated. Data will be obtained from patient journals in combination with measurements of REE and registration of survival. Data will be collected at one timepoint and survival will be monitored prospectively.

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Conditions studied

  • Cancer
  • Cachexia
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In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's enrollment of 160 is below the median of 204 across 1,683 observational studies indexed under Neoplasms.

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Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 487 studies on the registry; 52 are open to participants now.

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

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Who can participate

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

Study population

The population is patients diagnosed with an incurable malignant disease and hospitalized at the cancer clinic, St. Olavs Hospital in the period from september 2023 to june 2026. They have to be 18 years or older and able to provide written informed consent and comply with all study procedures.

Inclusion criteria

  • A verified diagnosis of an incurable malignant disease
  • Hospitalized at the Cancer clinic, St. Olavs Hospital
  • ≥ 18 years of age
  • Able to provide written informed consent
  • Able to comply with all study procedures

Exclusion criteria

Exclusion Criteria:

  • Cognitive impairment
  • In need of supplementary oxygen
  • Receiving invasive or noninvasive ventilation
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Study design

Observational model
Other
Time perspective
Other
Enrollment
160 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Measurement of resting energy expenditure (REE) in patients with incurable cancer measured with the COSMED Q-NRG+ Indirect Calorimeter with a Canopy Hood.

    Investigate the agreement between the most used energy expenditure prediction equation (Harris-Benedict calculation for resting energy expenditure based on weight, height and gender) and measured REE (kilocalories/day) by indirect calorimetry in patients with incurable cancer.

    Time frame: Throughout study completion, approximately 3 years.

Secondary outcomes

  1. Clinical factors associated with hyper- and hypometabolism

    Explore the association between patients identified as hyper-or hypometabolic (REE \> 10% or \< 10% of the predicted BMR (in kilocalories per day)) and a set of explanatory variables such as cancer diagnosis (type), weight loss last six months ((current/past weight)\*100), symptom score (Edmonton Symptom Assessment System (ESAS)), degree of inflammation (CRP in mg/L), and survival (days after REE measurement).

    Time frame: Throughout study completion, approximately 3 years.

07

Study locations

1 site
  • Cancer Clinic, St. Olavs Hospital, Trondheim University Hospital
    Trondheim, 7021, Norway
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06206785
Lead sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, UiT The Arctic University of Norway
Responsible party
Sponsor
First posted
Jan 16, 2024
Start date
Sep 5, 2023
Primary completion
Sep 23, 2025
Completion
Sep 30, 2026 (estimated)
Last update
Jun 29, 2026

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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