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The Altitude Inflammatory Bowel Disease Study

A Study on the Influence of Hypoxia on Healthy Volunteers and Patients With Inflammatory Bowel Disease (IBD): The Altitude IBD Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02849821
Enrollment
30
Registered
2016-07-29
Start date
2014-05-31
Completion date
2016-12-31
Last updated
2016-07-29

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

Conditions

Inflammatory Bowel Disease

Brief summary

This is a prospective, controlled and observational study. Participants underwent a 3-hour exposure to hypoxic conditions simulating an altitude of 4,000 meters above sea level (m.a.s.l.) in a hypobaric pressure chamber. Clinical parameters, as well as blood and stool samples and biopsies from the sigmoid colon (by sigmoidoscopy) are collected at subsequent time points. The investigators goal is to evaluate if a 3-hour stay at high altitude (4, 000 m) can alter disease activity and can modulate a pro inflammatory reaction.

Detailed description

To evaluate the potential influence of hypoxia on the course of IBD on a biomolecular level, and to test the effects of hypoxia under standardized conditions, the investigators initiated a prospective and controlled investigation in healthy controls and IBD patients in stable remission. the investigators primary aim is to show that a 3-hour stay at high altitude can alter disease activity of IBD. Ten healthy volunteers, 11 Crohn's disease (CD) patients and 9 ulcerative colitis (UC) patients underwent a 3-hour exposure to hypoxic conditions simulating an altitude of 4,000 m.a.s.l. in a hypobaric low-pressure chamber situated at the Swiss Aeromedical Center, Dubendorf, Switzerland. Stool samples for the analysis of calprotectin and microbiotal composition, biopsy samples from the rectosigmoid region, and blood samples were repetitively collected and analysed in conjunction with detailed records of clinical symptoms over a subsequent interval of 4 weeks.

Interventions

OTHERhypobaric pressure chamber

hypobaric chamber: ascent within 10 minutes, 3 hour exposure to hypoxic conditions simulating an altitude of 4,000 m.a.s.l., afterwards controlled descent under continuous pulsoximetric control

To retrieve biopsies from the colon during the course of the study 3 sigmoidoscopies were performed. The first sigmoidoscopy was performed 1 day before the stay in the hypobaric chamber. The second sigmoidoscopy was performed directly after the hypobaric chamber and the third sigmoidoscopy was performed 1 week after the hypobaric chamber. During each sigmoidoscopy 6 biopsies were taken with standard size forceps (2.4 mm). One biopsy was analysed by real-time quantitative polymerase chain reaction (PCR), one biopsy was analysed by Western blotting and another biopsy was analysed for gene gene-expression by in situ hybridisation. Two biopsies were analysed by immunohistochemistry (IHC) and one biopsy was stained with hematoxylin and eosin (H&E).

Sponsors

Triemli Hospital
CollaboratorOTHER
Zurich Center for Integrative Human Physiology
CollaboratorOTHER
Institute of Biostatistics
CollaboratorUNKNOWN
Insel Gruppe AG, University Hospital Bern
CollaboratorOTHER
Institute of Physiology Irchel
CollaboratorUNKNOWN
Institute of Veterinary Physiology
CollaboratorUNKNOWN
Swiss Aeromedical Center Switzerland
CollaboratorUNKNOWN
Institute of Experimental Immunology
CollaboratorUNKNOWN
University Hospital, Zürich
CollaboratorOTHER
University of Zurich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* had a diagnosis of Crohn's disease or ulcerative colitis at least 6 months prior to inclusion * gave written consent * were in clinical remission (measured by Harvey Bradshaw Activity Index (HBI) in CD and the partial Mayo Score for UC)

Exclusion criteria

* had contraindications for a sigmoidoscopy * had intercurrent bacterial or viral intestinal disease (by culture or serology) * were pregnant or breast feeding * had a severe concomitant disease which excluded from participating in the study by means of the study physician * were likely to or showed no cooperation for the study procedures * had active infection or systemic antibiotic, antiviral or antifungal treatment 3 weeks before baseline * were suffering from short-bowel syndrome * were receiving parenteral nutrition * had a clinical condition which did not allow a stay at heights of 4,000 m.a.s.l. * were claustrophobic

Design outcomes

Primary

MeasureTime frameDescription
Change of Harvey Bradshaw Activity Index (HBI)4 weeksHarvey Bradshaw Activity Index (HBI) in Crohn's disease (CD): To calculate the clinical activity of patients with CD the Harvey Bradshaw Activity Index (HBI) was used. This index includes general wellbeing, abdominal pain, the number of bowel movements, abdominal resistance and CD associated extraintestinal diseases. Each category has a point value assigned and from the sum of all categories a point value is calculated.
Change of partial Mayo Score4 weekspartial Mayo Score for Ulcerative Colitis (UC): To calculate the clinical activity of patients with UC the partial Mayo Score was used. This clinical index includes the stool frequency, the amount of blood in the stool and the physician rating of disease activity. Each category has a point value assigned from 0 to 3 and from the sum of all categories a point value was calculated. Remission is defined as 0-1 points, mild disease 2-4 points, moderate disease 5-6 points and severe disease as 7-9 points.

Secondary

MeasureTime frameDescription
Change in levels of angiotensin and vasopressin in urine4 weeks
Change in levels of catecholamines (adrenaline and noradrenaline) in blood4 weeks
change in levels of hypoxia-inducible factor (HIF)-14 weeks
Inflammation in sigmoid colon4 weeksAssessed by sigmoidoscopy: signs of inflammation: * decreased vascular pattern * ulcers * bleeding
Change in pro- and anti-inflammatory cytokins4 weekstumor necrosis factor alpha (TNF-α), tumor necrosis factor (TNF), interleukin-1β (IL-1β), interferon-gamma (IFNg), interleukin-10 (IL-10)
Change in bladder volume4 weeksmeasured by sonography (ml)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026