- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04637256
Evaluation of Outcomes From Treatment of Benign or Malignant Gastroesophageal Diseases
Study Overview
Status
Conditions
Detailed Description
INTRODUCTION 1.1. Background It is reported in the literature that the treatment of any gastroesophageal disease process, whether benign or malignant, continues to be a huge challenge. For example, patients with esophageal cancer continue to be diagnosed at an advanced stage with medical and surgical options that are improving in terms of outcome measurements but with much more room for improvement. The Primary investigtor goal is to continue to review patient treatment outcomes to further improve overall survival, overall symptom control, mortality and morbidity.
1.2. Aim(s)/Objective(s) The main aim of this study is to evaluate and compare the outcomes from the investigator's treatment of benign or gastroesophageal diseases.
1.3. Rationale for the study There is a need to understand and improve the current diagnosis and treatment algorithm for gastroesophageal pathologies. Continued evaluation and study is imperative to ensure that national guidelines are improving to enhance patient cure and/or recovery.
OBJECTIVES AND STUDY OUTCOME MEASURES 2.1. Study Objectives 2.1.1. Primary Objective(s)
- To evaluate and compare the outcomes from the investigator's treatment of benign or malignant gastroesophageal disease 2.2. Study Outcome Measures 2.2.1. Primary Outcome(s)
To exam all treatments of benign or malignant gastroesophageal disease by measuring the following outcomes
- Overall survival
- Overall symptom control
- Mortality
- Morbidity
4. STUDY ENROLLMENT AND WITHDRAWAL 4.1. Study Inclusion Criteria:
- All patients diagnosed and treated for gastroesophageal diseases, benign or malignant from 2005 to present.
- Age ≥18 years 4.2. Study Exclusion Criteria:
- Patients that are not diagnosed with or treated for gastroesophageal diseases
- Age < 18 years 5. STATISTICAL CONSIDERATIONS 5.1. Sample Size Considerations All past patients who were treated for a particular benign or malignant gastroesophageal disease process under evaluation from 2005 to present will be included in this study.
5.2. Statistical Analysis Plan Statistics will be provided for all data obtained. Normally distributed continuous outcomes will be analyzed with Student's t test and non-normally distributed continuous outcomes will be analyzed with nonparametric Wilcoxon-Mann-Whitney test. Categorical outcomes will be analyzed using chi-square test or Fisher's exact test for smaller samples.
6
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Texas
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Richardson, Texas, United States, 75082
- Trinity Surgical Consultants, Methodist Richardson Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients diagnosed and treated for gastroesophageal diseases, benign or malignant from 2005 to present.
- Age ≥18 years
Exclusion Criteria:
- Patients that are not diagnosed with or treated for gastroesophageal diseases
- Age < 18 years
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Overall Survival
Time Frame: 2005 to 2019
|
We will be examining all treatments of benign or malignant pancreatic cancer by measuring the following outcome: overall survival
|
2005 to 2019
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Dhiresh Jeyarajah, M.D., Methodist Health System
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 037.HPB.2018.R
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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