A steroid-sparing strategy: could olanzapine curb chemo nausea without the metabolic toll?
NCT ID NCT07743827
First seen Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time
Summary
This trial tests whether olanzapine can replace dexamethasone in preventing delayed nausea and vomiting after chemotherapy in breast cancer patients who have metabolic risk factors like diabetes or obesity. Participants receive either an olanzapine-based regimen or the standard dexamethasone-containing regimen, and researchers compare how well each controls symptoms and affects blood sugar and insulin resistance. The goal is to find an equally effective anti-nausea approach with fewer metabolic side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- olanzapine
- What this could lead to
- If successful, this could offer a safer anti-nausea approach for breast cancer patients with metabolic issues, reducing steroid-related blood sugar and insulin problems.
- What could go wrong
- The trial is small and early, and olanzapine may not control nausea as well as dexamethasone. It also has its own side effects like sedation, and results may not apply to all patients.
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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About 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female patients ≥18 years. * Stage I-III breast cancer. * Scheduled to receive AC chemotherapy. * Presence of metabolic risk factors (diabetes, prediabetes, obesity, metabolic syndrome). * ECOG performance status ≤2. Exclusion Criteria: * Recent systemic corticosteroid use. * Active nausea or vomiting before chemotherapy. * Severe renal or hepatic impairment. * Uncontrolled diabetes or hypertension. * Psychiatric illness affecting adherence. * Pregnancy or lactation. * Active infections or inflammatory diseases. * Participation in another clinical trial
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Alexandria Main University Hospital
RECRUITINGAlexandria, Alexandria Governorate, 21526, Egypt
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Other studies related to the condition(s) this trial covers.
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- Can an oral drug replace injections for advanced breast cancer?
- Can a common steroid shield breast cancer patients from a dangerous drug side effect?