Can Real-World data improve esophageal cancer care in africa?
NCT ID NCT05177393
First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time
Summary
This observational study follows over 2,400 people with esophageal cancer across multiple African hospitals to see which treatments they receive and how they fare. Researchers will track symptoms, quality of life, and survival over time. The goal is to understand what works best in real-world, resource-limited settings.
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 reveal which treatment strategies work best for esophageal cancer in resource-limited settings, guiding future care.
- What could go wrong
- This is an observational study, not a controlled trial, so it cannot prove one treatment is better than another. Results may be affected by differences in patient health and access to care.
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 2,476 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2019
- Expected to finish
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Jun 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
Participants with esophageal cancer based on histological confirmation or presumptive clinical diagnosis who reside in Kenya, Tanzania, and Malawi.
- 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: * Participants with histopathologically confirmed or presumptive clinical diagnosis of EC. For patients who do not have histopathologically confirmed disease, presumptive clinical diagnosis may be based upon barium swallow or endoscopy without biopsy. * Age 18 years of age or older; Exclusion Criteria: * Unable to provide informed consent
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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
6 sites in 3 countries. 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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Kamuzu Central Hospital
RECRUITINGLilongwe, Malawi
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Kilimanjaro Christian Medical Centre
RECRUITINGMoshi, Tanzania
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Moi Teaching and Referral Hospital
RECRUITINGEldoret, Kenya
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Muhimbili National Hospital
RECRUITINGDar es Salaam, Tanzania
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Ocean Road Cancer Institute
RECRUITINGDar es Salaam, Tanzania
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Tenwek Hospital
RECRUITINGBomet, Kenya
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Other studies related to the condition(s) this trial covers.
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- A single blood draw to detect five cancers before symptoms appear?
- Can custom vitamin pills fix nutrient gaps after stomach or esophageal cancer surgery?
- Can repeated MRI scans reveal how tumors respond to radiation?