Mayo Clinic Conduit Report Card Questionnaires (CONDUIT) (CONDUIT)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02530983|
Recruitment Status : Recruiting
First Posted : August 21, 2015
Last Update Posted : October 3, 2019
|Condition or disease||Intervention/treatment|
|Esophageal Neoplasms Cancer of Esophagus Cancer of the Esophagus Esophageal Cancer Esophagus Cancer Neoplasm, Esophageal Esophagectomy||Other: Mayo Clinic Conduit Report Card Questionnaires|
|Study Type :||Observational|
|Estimated Enrollment :||1000 participants|
|Official Title:||Mayo Clinic Conduit Report Card Questionnaires|
|Study Start Date :||August 2015|
|Estimated Primary Completion Date :||December 2020|
|Estimated Study Completion Date :||December 2020|
Patients who have undergone esophagectomy or esophageal reconstruction
Other: Mayo Clinic Conduit Report Card Questionnaires
Patients will be asked to complete the Mayo Clinic Conduit Report Card Questionnaires at their one month surgical follow up visit and then every three months for 1 year after surgery, then with each surveillance clinic visit or a minimum of once per year for their lifetime. The questionnaire can be completed at their clinic visit, over the telephone, or by mail. The patient's medical record will also be reviewed to gather any other contributing information.
- Completion of the Mayo Clinic Conduit Report Card Questionnaires by patients at varying time points following surgery [ Time Frame: 1 year ]Completed Mayo Clinic Conduit Report Card Questionnaires will be analyzed and used to establish validation.
- Establishment of "normal" or expected scores from the Mayo Clinic Conduit Report Card Questionnaires [ Time Frame: 3 years ]Completed Mayo Clinic Conduit Report Card Questionnaires will be used in the establishment of "normal" or expected scores for patients undergoing each type of esophagectomy procedure at different time points following surgery.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02530983
|Contact: Karlyn Pierson, MAN, RNemail@example.com|
|Contact: Bettie Lechtenberg, MBAfirstname.lastname@example.org|
|United States, Minnesota|
|Rochester, Minnesota, United States, 55901|
|Contact: Karlyn Pierson, MAN, RN 507-538-1960 email@example.com|
|Contact: Bettie Lechtenberg, MBA 507-266-4819 firstname.lastname@example.org|
|Principal Investigator: Shanda Blackmon, MD, MPH, FACS|
|Principal Investigator:||Shanda Blackmon, MD, MPH, FACS||Mayo Clinic|