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Enrolling by invitation NCT05115877

Evaluation of Outcomes From Treatment of Benign or Malignant Gastrointestinal Diseases

Observational Gastrointestinal Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Gastrointestinal Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study will be a retrospective, registry study collecting data of patients who were diagnosed with benign or malignant gastrointestinal diseases. Data will be collected from patient's chart retrospectively once the patients have completed proper treatment follow up with physicians' practice.

Detailed description

It is reported in the literature that the treatment of any gastrointestinal disease process, whether benign or malignant, continues to be a huge challenge. For example, patients with gastrointestinal 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 goal is to continue to review our treatment outcomes to further improve overall survival, overall symptom control, mortality and morbidity.

The main aim of this study is to evaluate and compare the outcomes from our treatment of benign or malignant gastrointestinal diseases through medical chart review.

There is a need to understand and improve the current diagnosis and treatment algorithm for gastrointestinal pathologies. Continued evaluation and study is imperative to ensure that national guidelines are improving to enhance patient cure and/or recovery.

Primary outcome measures

  • Overall survival [Time frame: Jan 2005 - Jan 2030]
  • Overall symptom [Time frame: Jan 2005 - Jan 2030]
  • Mortality [Time frame: Jan 2005 - Jan 2030]
  • Morbidity [Time frame: Jan 2005 - Jan 2030]

Eligibility criteria

Inclusion criteria

  • All patients diagnosed and treated for gastrointestinal diseases, benign or malignant from 2005 to 2030.
  • Age ≥18 years

Exclusion criteria

  • Patients that are not diagnosed with or treated for gastrointestinal diseases
  • Age <18 years

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

United States · 1 center
  • Methodist Richardson Medical Center — Richardson

Identifiers

NCT: NCT05115877 · 031.HPB.2020.R

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗