Fasting may soothe aromatase inhibitor side effects
NCT ID NCT06172088
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a 7-day supervised fast (max 350 calories per day) could reduce muscle and joint pain in 54 breast cancer patients taking aromatase inhibitors. The goal was to see if fasting is feasible and improves physical well-being and quality of life. Researchers also tested a new app to track symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- therapeutic fasting (7-day prolonged fast, max 350 kcal/day)
- What this could lead to
- If it works, this could offer a drug-free way to reduce muscle and joint pain for breast cancer patients on hormone therapy.
- What could go wrong
- This is a small, early exploratory study with only 54 participants, so results may not apply widely. Fasting can be hard to stick with and may not be safe for everyone.
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
-
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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54 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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Sep 2025
- 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 70 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 curatively treated hormone receptor positive breast cancer who have been on aromatase inhibitors (AI) therapy for at least 3 months and have significant Pain (NRS\>4). * Informed consent. Exclusion Criteria: * Eating disorders. * Permanent medication other than endocrine therapy, which would constitute an absolute or relative contraindication to outpatient fasting, such as Marcumar, lithium, Antiepileptic drugs, etc. * Patients with diabetes mellitus type 1 or 2 * Uncontrolled cerebral seizure disorder. * Participation in another diet/fasting study. * Lack of willingness to store and share personal medical data within the framework of the protocol. * Insufficient knowledge of the German language.
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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
-
Robert-Bosch-Krankenhaus
Stuttgart, Baden Würtenberg, 70341, Germany
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Würzburg University
Würzburg, Bavaria, 97080, Germany
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