Recruiting

Radiation

Sponsor:

University of Texas Southwestern Medical Center

Code:

NCT03617237

Conditions

Cancer

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Retrospective Populations

Study Details

Brief summary:

Registry database repository for determining clinical outcomes primarily of patients who have received or have been evaluated for radiation treatment in either the definitive or palliative setting for both malignant and benign etiologies.

To compare the outcomes with National Cancer Data Base (NCDB) of the American College of Surgeon(ACS).

Conditions

Cancer

Study ID

NCT03617237

Start date

Jul 3, 2012

Status verified date

Apr, 2026

Completion date

Apr 18, 2032

Anticipated

Primary completion date

Jul 10, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

Any patient who received or was potentially evaluated for radiotherapy since 2000 for benign or malignant etiologies in the definitive or palliative setting.

Patients with comparatively similar diagnosis and disease status at UTSW, but electing not to undergo radiation therapy, treated with surgical or systemic therapy, or best supportive care, being followed by an oncology specialist at UT Southwestern Medical Center will also be eligible for evaluation. -

Exclusion Criteria:

None

Study Design

Enrollment

10000 participants

Anticipated

Interventions and Outcome Measures

Interventions

Retrospective Populations

All patients who are currently treated by any physician at the University of Texas Southwestern campus Aston Clinic, Seay Clinic, PHHS Clinic, Moncrief Radiation Oncology, St. Paul West Campus Radiation Oncology, East Radiation Oncology Clinic will be included in the registry. The data from the charts will be entered into a password protected excel spreadsheet. The charts will be identified by name, medical record number, date of birth, and social security number.

1. The research involves no more than minimal risk to the subjects.
2. The waiver will not adversely affect the rights and welfare of the subjects.
3. The research could not practicably be carried out without the waiver.
4. Whenever appropriate, the subjects will be provided with additional pertinent information after participation.

Primary outcome measure

  • Quality of Life Analysis [ Time Frame: 10 years ]

Central Contacts and Locations

Central contacts

Sarah Neufeld, MS

2146458525sarah.hardee@utsouthwestern.edu

David J Sher, MD, MPH

214-645-8525David.Sher@UTSouthwestern.edu

Locations

UT Southwestern Medical Centre

Recruiting

Dallas, Texas, United States, 75390

Contacts

Sarah Neufeld, MS

214-648-1836Sarah.Hardee@UTSouthwestern.edu

More Information

Sponsor

University of Texas Southwestern Medical Center

Last update posted

Apr 17, 2026

Last verified

Apr, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Texas Southwestern Medical Center on 2026-04-17.