Breast cancer trial halted after just 2 patients enrolled
NCT ID NCT02688803
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to test a simpler consent process to compare three standard chemotherapy regimens for triple-negative breast cancer. Only 2 participants enrolled before the trial was terminated early, so it could not determine which treatment works best. The main goal was to see if this new consent model was feasible, not to find a cure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- chemotherapy (doxorubicin, cyclophosphamide, paclitaxel, 5-FU, epirubicin, docetaxel)
- What this could lead to
- If successful, this approach could make it easier to compare standard treatments in real-world settings, helping doctors choose the best chemotherapy for triple-negative breast cancer.
- What could go wrong
- The trial was terminated early with only 2 participants, so it did not gather enough data to draw meaningful conclusions. The results may not apply to broader populations.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
2 people
The number who actually took part.
- Started
-
Aug 2016
- Finished
-
Oct 2017
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
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: * Histologically confirmed primary TNBC breast cancer * Planned for chemotherapy * ≥18 years of age * Able to provide verbal consent * Willing to complete a survey Exclusion Criteria: * Metastatic disease * Contraindication to one or more of the chemotherapy agents being evaluated in the study
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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
-
The Ottawa Hospital Cancer Centre
Ottawa, Ontario, K2H 8L6, Canada
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