Discovering Patterns in Experiences of Patients in Esophageal Cancer Clinical Research
Investigating Factors Affecting Clinical Trial Participation Rates in Patients With Esophageal Cancer
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Participation in clinical trials usually favors a particular demographic group. But there is limited research available to explain what study attributes affect the completion of these specific demographic groups. This study will investigate the safety and efficacy of esophageal cancer treatments. The focus will be on tracking the rates of completion and withdrawal among these individuals. It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future esophageal cancer research.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 14, 2023
CompletedFirst Posted
Study publicly available on registry
April 26, 2023
CompletedStudy Start
First participant enrolled
May 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedApril 26, 2023
April 1, 2023
1 year
April 14, 2023
April 14, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Rate of patients who decide to enroll in a clinical research.
3 months
Number of study participants who remain in clinical research until completion.
12 months
Eligibility Criteria
Patients who are actively considering involvement in an observational esophageal cancer clinical trial, but have not yet completed enrollment and registration.
You may qualify if:
- Patient is at least 18 years of age
- Diagnosis of esophageal cancer
- Ability to understand a written informed consent document, and the willingness to sign it.
You may not qualify if:
- Women of childbearing potential without a negative pregnancy test; or women who are lactating.
- Has a serious medical or psychiatric illness likely to interfere with participation in this clinical study.
- Inability to perform regular electronic reporting
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Kim HJ, Bains MS. Randomized clinical trials in esophageal cancer. Surg Oncol Clin N Am. 2002 Jan;11(1):89-109, viii. doi: 10.1016/s1055-3207(03)00076-0.
PMID: 11928803BACKGROUNDHarada K, Rogers JE, Iwatsuki M, Yamashita K, Baba H, Ajani JA. Recent advances in treating oesophageal cancer. F1000Res. 2020 Oct 1;9:F1000 Faculty Rev-1189. doi: 10.12688/f1000research.22926.1. eCollection 2020.
PMID: 33042518BACKGROUNDZhou N, Hofstetter WL. Prognostic and therapeutic molecular markers in the clinical management of esophageal cancer. Expert Rev Mol Diagn. 2020 Apr;20(4):401-411. doi: 10.1080/14737159.2020.1731307. Epub 2020 Feb 24.
PMID: 32067548BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Michael B Gill
Power Life Sciences Inc.
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 14, 2023
First Posted
April 26, 2023
Study Start
May 1, 2024
Primary Completion
May 1, 2025
Study Completion
May 1, 2026
Last Updated
April 26, 2023
Record last verified: 2023-04