Portable DNA reader could slash breast cancer diagnosis time in tanzania
NCT ID NCT06633276
First seen Sep 23, 2026 · Last updated Oct 16, 2026 · Updated 2 times
Summary
Researchers in Tanzania are testing whether a portable DNA-reading technology called nanopore sequencing can diagnose invasive breast cancer as accurately as standard lab tests, but faster and at lower cost. The study enrolls 100 patients with suspected breast cancer who are undergoing a biopsy or surgery. Scientists will compare nanopore results with standard hormone and HER2 testing, measure how long each method takes, and track patients' quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nanopore sequencing, a portable DNA-reading technology used to analyze tumor samples
- What this could lead to
- If nanopore sequencing matches standard lab tests, it could give patients in Tanzania faster, cheaper breast cancer diagnoses and speed up treatment planning.
- What could go wrong
- This is a small pilot study of 100 patients in one country, so the results may not hold up in larger or different settings. The technology may fail to produce usable results from some biopsy samples.
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.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 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.
Who is studied
All patients with suspected invasive breast cancer undergoing diagnostic workup will be offered to participate.
- Ages
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18 years and older
- Sex
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Anyone
- 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: * Patient with suspected diagnosis of breast cancer undergoing biopsy or surgical resection after specialist consultation as per institutional guidelines * Excess fresh tumor sample * Written informed consent Exclusion Criteria: * Unable to provide informed consent * Patients who have already commenced therapy for BC (except for treatment other than biomedicine, e.g. herbal medicines)
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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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Kilimanjaro Christian Medical Centre
RECRUITINGMoshi, P.O. Box 3010, Tanzania
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