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Status unknownNCT02275676CEDERN-1Updated Oct 27, 2014

Resting Energy Expenditure and Nutritional Status in IBD

An observational study in Inflammatory Bowel Disease and Malnutrition, sponsored by University Hospital Muenster. Status unknown at 1 site in Germany. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2014-10-27.

Sponsored by University Hospital Muenster · Observational

The sponsor has not verified this record recently (last verified Oct 2014), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Nutrient deficiencies occur frequently in IBD patients. The absorption rate of nutrients in IBD is often limited by chronic inflammation, but is also commonly reduced by missing intestinal segments due to previous operations. Patients are predominantly affected by malnutrition, which is often resembled by weight loss, specific micronutrient deficits such as iron deficiency, vitamin B12 deficiency, folic acid deficiency, vitamin D deficiency and zinc depletion. The etiology of nutritional problems is multifactorial and not exclusively limited to active phases of the disease. Causes of malnutrition can be inadequate food intake, maldigestion, malabsorption or increased nutritional requirement. Malnutrition itself is associated with a delayed recovery of impaired wound healing, reduced quality of life and longer hospital stays. Therefore, observation and modification of the nutritional status should be an integral part of therapy in IBD patients.

The primary objective of our study is to investigate the influence of the disease on the resting energy expenditure and nutritional status during acute inflammation and clinical remission of the disease. Secondary objectives are to assess possible nutritional deficiencies. On the other hand it is well known that patients with IBD are at increased risk for coronary heart disease. Therefore, another secondary focus of our observational study is whether the composition of the HDL proteins is changed towards pro-atherogenic HDL-proteins and whether possible changes occur in patients in clinical remission or with active disease.

Read the detailed description

Primary objective of the study is to investigate the influence of the disease activity on the resting energy expenditure and the nutritional status in patients with chronic inflammatory bowel disease (IBD). The impact of IBD on the nutritional status and the resting energy expenditure is currently not fully understood. IBD includes two different disease entities, Crohn's disease and ulcerative colitis. Both are characterized by diarrhea, loss of weight, rectal bleeding and abdominal discomfort (abdominal pain, flatulence). In patients with IBD malabsorption, one-sided nutritional behavior, food abandonment, malnutrition, nutrient deficiency and weight loss are common issues. Malnutrition is associated with delayed recovery, impaired wound healing, reduced quality of life and prolonged hospital stay. The malnutrition is not limited to active disease state. Rates for malnutrition in patients with Crohn's disease range from 20 - 85%. Hence, the assessment of the nutritional status is important in the treatment of patients with IBD. Different methods are used to assess the impact of the disease activity on the nutritional status. To investigate the resting energy expenditure the well evaluated indirect calorimetry is used. The principle of the measurement is based on determination of the oxygen absorption during inspiration and the simultaneous determination of the release of carbon dioxide during expiration. The use of bioelectrical impedance analysis (BIA) is a widespread measurement to assess the composition of the body. BIA allows the determination of the fat-free mass, total body water, body cell mass, fat mass and extracellular mass.

Both measurements are non-invasive and reproducible. Additionally different blood parameters are determined such as HDL-subgroups, vitamin b12, folic acid, vitamin K, vitamin D, 25-hydroxy-vitamin D3, zinc, ferritin, albumin, citrulline and routine laboratory (blood count, serum chemistry, coagulation) . Moreover the quality of life is measured through a suitable questionnaire (Gastrointestinal Life Quality Index) as well as the subjective global assessment to estimate the nutritional status.

Furthermore, a secondary aim of the study is to investigate the correlation of HDL-subgroups and the severity of the IBD activity. High-Density-Lipoproteins are a heterogeneous group of lipoproteins with both anti-atherogenic and multiple anti-inflammatory properties. Recent research showed that the quality of HDL-particle is even more important than the quantity. It could be shown that changes in the composition of the HDL could cause an inflammatory status and thus affect the activity of chronic inflammatory disease. Therefore, it is the aim of the study to investigate if changes in the composition of HDL-proteins towards pro-atherogenic HDL-proteins exist.

The study will take place at the University Hospital of Muenster, Germany. Patients who are suitable for participating in the study will be measured and counseled during their regular out-clinic visits. Each patient has to undergo the procedure while they are in an active state of the disease and during remission. It is expected to include 200 patients over 2 years.

02

Conditions studied

  • Inflammatory Bowel Disease
  • Malnutrition

Keywords

  • Inflammatory bowel disease
  • Nutritional Status
  • Malnutrition
  • Resting Energy Expenditure
03

In context

Intestinal Diseases

963 studies on the registry are indexed under Intestinal Diseases; 174 are open to participants now.

This study's planned enrollment of 200 is above the median of 140 across 377 observational studies indexed under Intestinal Diseases.

Browse Intestinal Diseases studies →

Lead sponsor

University Hospital Muenster is the lead sponsor of 189 studies on the registry; 18 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with active or inactive inflammatory bowel disease at our medical tertiary referral center, Muenster Germany

Inclusion criteria

  • inflammatory bowel disease
  • male and female between 18-80 years
  • patient fully able to understand the study concept and to give his or her written consent

Exclusion criteria

Exclusion Criteria:

  • underlying malignant disease
  • Diabetes mellitus, Type I or II
  • Pregnancy
  • Lactating
  • chronic alcohol or drug abuse
  • known anorexia nervosa or binge eating disorder
  • known metabolic disorders, such as e.g. Cushing disease, hypothyroidism
  • Participation in other interventional studies within the last 6 months prior to study enrollment
  • patient not fully able to understand the study concept and to give his or her written consent
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No

Groups and cohorts

  • Inflammatory bowel disease

    Patients with active and inactive inflammatory bowel disease

    Other: bioelectrical impedance analysis · Other: indirect calorimetry

Interventions

  • Otherbioelectrical impedance analysis
  • Otherindirect calorimetry
06

What researchers measure

Primary outcomes

  1. change in bioelectrical impedance analysis (BIA)

    e.g. fat free mass, total body water, body cell mass

    Time frame: change from baseline in BIA at 6 month and at 12 month

  2. Change in resting energy expenditure (REE)

    Resting energy expenditure measured by indirect calorimetry (kcal per day)

    Time frame: change from baseline in REE at 6 month and at 12 month

Secondary outcomes

  1. change in HDL subgroup analysis

    Time frame: day 1, every 6 month up to 12 month

  2. change in plasma citrulline level

    Time frame: day 1, every 6 month up to 12 month

  3. change in plasma vitamine levels and plasma zinc level

    Vitamin B12, Vitamin K, Vitamin D

    Time frame: day 1, every 6 month up to 12 month

Other outcomes

  1. change in fecal Calprotectin level

    Time frame: day 1, every 6 month up to 12 month

  2. change in live quality questionnaire

    Gastrointestinal Quality of Life Index by Eypasch

    Time frame: day 1, every 6 month up to 12 month

07

Study locations

1 of 1 sites recruiting
  • University Hospital Muenster
    Muenster, 48149, Germany
    • Frank Lenze, Dr. · Principal investigator
    • Hauke Heinzow, Dr. · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 27, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02275676
Lead sponsor
University Hospital Muenster
Responsible party
Dr. med. Hauke Heinzow (Doktor, University Hospital Muenster) — Principal investigator
First posted
Oct 27, 2014
Start date
Sep 2014
Primary completion
Sep 2016 (estimated)
Completion
Sep 2016 (estimated)
Last update
Oct 27, 2014

Study contacts

Frank Lenze, Dr.
Contact
frank.lenze@ukmuenster.de
+49-251-8358103
Hauke Heinzow, Dr.
Contact
hauke.heinzow@ukmuenster.de
+49-251-8347661
Frank Lenze, Dr.
principal investigator · University Hospital Muenster, Germany
Hauke Heinzow, Dr.
principal investigator · University Hospital Muenster, Germany

Oversight

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

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