Actively Recruiting
Mayo Clinic Upper Digestive Disease Survey for Patients Undergoing Esophageal Surgery or Treatment
Led by Mayo Clinic · Updated on 2026-03-30
1000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating standardized questionnaires called the Mayo Clinic Conduit Report Card Questionnaires to consistently assess patients who have undergone esophageal reconstruction or treatment, or who have upper digestive diseases. The goal is to validate these questionnaires and establish normal or expected scores for different types of esophagectomy procedures and upper digestive conditions. This data will help develop treatment guidelines for symptom management, post-operative complications, and support pre-operative patient education. The study involves patients completing the Mayo Clinic Upper Digestive Disease Survey, which combines several validated patient and provider-reported questionnaires. Patients complete the survey at their one-month surgical follow-up, then every three months for one year after surgery, followed by annual or surveillance visits for life. The survey can be done during clinic visits, by phone, mail, or electronically through an app available for both Mayo Clinic and non-Mayo Clinic patients. Participants provide information on demographics, surgeries, nutrition, lab tests, and clinical outcomes. Researchers collect data through questionnaires and medical record reviews at scheduled intervals. The main outcome measure is the completion of the survey at different times post-surgery over one year, with secondary outcomes including defining normal scores over three years. Participation may continue yearly for life, allowing ongoing monitoring of upper digestive symptoms and outcomes.
CONDITIONS
Brief Title
Mayo Clinic Upper Digestive Disease Survey
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing or having already undergone an esophagectomy or esophageal reconstruction.
You will not qualify if you...
- None specified in the eligibility criteria provided; no explicit exclusion criteria listed.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to lifetime
Participants complete the Mayo Clinic Upper Digestive Disease Survey at specific follow-up times after surgery or diagnosis, and then with each surveillance clinic visit or at least once per year for their lifetime. The survey can be completed in clinic, by telephone, mail, or electronically via an app.
At 1 month post-surgical or diagnosis follow-up, then every 3 months for 1 year, followed by annual visits or surveillance clinic visits
Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55901
Actively Recruiting
Research Team
M
Mohamad Khair Abou Chaar, MD
K
Karlyn Pierson, MAN, RN
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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