Starving the gut: anorexia may damage intestinal barrier
NCT ID NCT02170467
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study checked whether the gut lining becomes leaky in women with anorexia nervosa due to severe starvation. Researchers measured sugar levels in urine after drinking special sugars to test intestinal permeability in 23 patients and compared them to 46 healthy controls. They also looked at certain antibodies and gut bacteria changes before and after refeeding. The goal is to understand how malnutrition affects the gut barrier in anorexia.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help explain how starvation affects the gut barrier in anorexia nervosa, potentially guiding future treatments.
- What could go wrong
- This is a small, observational study with only 23 patients, so results may not apply to everyone. It does not test any treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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51 people
The number who actually took part.
- Start date
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Jan 2015
- Finished
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May 2018
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 50 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients with anorexia nervosa : * female, * living in Upper Normandy since 1 year at least, * between 18 and 50 years of age * with a BMI between 14 and 16 kg/m², * diagnosed as anorexia nervosa according to the DSM IV criteria * hospitalised for the first time in the Nutrition Unit * not being pregnant (effective contraception and negative pregnancy test) * not breast-feeding, * HIV-1 negative , * HIV-2 negative, * HBV negative (hépatitis B virus), * HCV negative (hépatitis C virus), * Affiliated to the National Health Service, * Giving a filled informed consent, * Not included in other studies Controls : * female, * living in Upper Normandy since 1 year at least, * between 18 and 50 years of age, * with a BMI between 20 and 24,9 kg/m², * without antecedent or current diagnosis of eating disorders (DSM IV criteria), * without dyspepsia or irritable bowel syndrom for 6 month, * not being pregnant (effective contraception and negative pregnancy test) * not breast-feeding, * HIV-1 negative , * HIV-2 negative, * HBV negative (hépatitis B virus), * HCV negative (hépatitis C virus), * Affiliated to the National Health Service, * Giving a filled informed consent, * Not included in other studies Exclusion Criteria: Patients with anorexia nervosa : * Adult under guardianship, * Patient with inflammatory bowel disease and/or psychotic disorders, * Antecedent of digestive surgery, * Drug addiction for the last 6 month, * Alcohol and/or other substance use disorder, * Current immunological treatment, and/or non steroidal anti inflamatory and/or corticosteroids and/or anticoagulants and/or platelet antiaggregants * galactosemia * Lactulose intolerance, * Laxatives intake in the last 3 days * Antecedent of digestive surgery, Controls : * Adult under guardianship, * Patient with inflammatory bowel disease and/or psychotic disorders, * Antecedent of digestive surgery, * Drug addiction for the last 6 month, * Alcohol and/or other substance use disorder, * Current immunological treatment, and/or non steroidal anti inflamatory and/or corticosteroids and/or anticoagulants and/or platelet antiaggregants * galactosemia * Lactulose intolerance, * Laxatives intake in the last 3 days * Antecedent of digestive surgery,
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU- Hôpitaux de Rouen
Rouen, 76031, France
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Hôpital de la Croix Rouge
Bois-Guillaume, 76233, France
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Other studies related to the condition(s) this trial covers.
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