CClinicalTrials.gg
CompletedNCT00877045Updated Aug 4, 2010

Treatment Patterns in Gastrointestinal Stromal Tumors in the Community Oncology Setting

An observational study in Gastrointestinal Stromal Tumors, sponsored by SCRI Development Innovations, LLC. Completed at 5 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-08-04.

Sponsored by SCRI Development Innovations, LLC · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
200
Ages
18 Years and older
Sex
All
01

Study summary

This is a retrospective medical record abstraction to evaluate the patterns of care for Gastrointestinal stromal tumors (GIST) in the community setting. Patient demographics and characteristics along with the treatments received will be described. Investigators will establish the percentage of patients who undergo surgery, the percentage of patients who are treated with kinase inhibitors as well as in what setting (adjuvant or metastatic) as well as the duration of therapy. Physician information will also be collected to assess for differences in treatment based on physician or geographical differences.

02

Conditions studied

  • Gastrointestinal Stromal Tumors

Keywords

  • Gastrointestinal Stromal Tumors
  • GIST
  • tyrosine kinase inhibitors
  • Imatinib
  • Gleevec
  • Suntinib
  • Sutent
03

In context

Gastrointestinal Stromal Tumors

333 studies on the registry are indexed under Gastrointestinal Stromal Tumors; 61 are open to participants now.

This study's enrollment of 200 is above the median of 116 across 68 observational studies indexed under Gastrointestinal Stromal Tumors.

Browse Gastrointestinal Stromal Tumors studies →

Lead sponsor

SCRI Development Innovations, LLC is the lead sponsor of 174 studies on the registry; 5 are open to participants now.

Of its 15 completed or terminated interventional studies of FDA-regulated products, 15 (100%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients diagnosed with GIST based on ICD-9 code from January 2005 to present will be eligible. This will include current active patients as well as patients who have expired and have medical chart available. Estimate reviewing approximately 300 charts total.

Eligibility criteria

Inclusion Criteria:

  • Patients diagnosed with GIST based on ICD-9 code from January 2005 to present will be eligible. This will include current active patients as well as patients who have expired and have medical chart available.
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
200 participants (actual)
06

Study locations

5 sites
  • Florida Cancer Specialists
    Fort Myers, Florida 33901, United States
  • Georgia Cancer Specialists
    Atlanta, Georgia 30341, United States
  • Chattanooga Oncology Hematology Associates
    Chattanooga, Tennessee 37404, United States
  • Tennessee Oncology, PLLC
    Nashville, Tennessee 37023, United States
  • Virginia Cancer Institute
    Richmond, Virginia 23235, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00877045
Lead sponsor
SCRI Development Innovations, LLC
Collaborators
Pfizer
First posted
Apr 7, 2009
Start date
Jan 2008
Primary completion
Jan 2009
Completion
Feb 2009
Last update
Aug 4, 2010

Study contacts

Jeffrey F Patton, M.D.
study chair · SCRI Development Innovations, LLC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2010. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion