Can a smartphone app cut complications after esophageal cancer surgery?
NCT ID NCT07211009
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a patient-reported symptom app can improve recovery after esophageal cancer surgery. 240 patients will either use the app to report symptoms or receive standard care. The goal is to see if the app reduces complications and improves 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
- Patient-Reported Outcome (PRO)-Based Symptom Management via WeChat mini-program
- What this could lead to
- If successful, this could show that using a simple app to track symptoms helps patients recover better after esophageal cancer surgery, reducing complications and improving quality of life.
- What could go wrong
- This is a single-center trial in China, so results may not apply to other settings. The intervention is a monitoring tool, not a drug, so it may not directly change disease outcomes.
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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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 240 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
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 75 years
- 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: 1. Age 18-75 years. 2. Pathologically confirmed esophageal cancer. 3. Planned to undergo curative (radical) surgical resection. 4. R0 resection. 5. Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 1. 6. Adequate function of major organs. 7. Willing to complete questionnaire surveys. 8. Voluntarily agrees to participate and signs the informed consent form. 9. Good compliance and able to complete follow-up as scheduled. Exclusion Criteria: 1. Human immunodeficiency virus (HIV) infection. 2. Psychiatric disorder. 3. Any other malignancy within the past 5 years (except completely cured carcinoma in situ of the cervix or basal cell/squamous cell carcinoma of the skin). 4. Patient ultimately did not undergo curative (radical) surgical resection. 5. Any unstable systemic disease (including active, uncontrolled gastrointestinal ulcer; active infection; grade 4 hypertension; unstable angina; congestive heart failure; unstable cerebrovascular disease; thrombotic disease; hepatic, renal, or metabolic disease; or unhealed fracture/wound as determined by the surgeon). 6. Difficulty in communication or inability to comply with long-term follow-up. 7. Any other condition deemed unsuitable by the investigator.
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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