A Prospective Analysis of Active Observation in Patients With Desmoid-Type Fibromatosis

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The purpose of this study is to closely observe people with desmoid-type fibromatosis over 1 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Clinical diagnosis of desmoid fibromatosis, either new or newly recurrent. Both patients with sporadic and FAP-associated disease will be eligible for inclusion. Patients with clinical diagnosis of desmoid (as assessed by MSK physician) but without pathologic diagnosis may be enrolled on the study to facilitate acquisition of appropriately protocoled baseline scans and allow for biospecimen collection; these patients will be replaced for purposes of analysis if pathology does not confirm clinical diagnosis.

• At least 18 years of age.

• Able to undergo cross-sectional imaging by either MRI or CT with intravenous contrast

• Disease detectable on cross-sectional imaging with target lesion measuring \>/= 1 cm

• Eligible for management by active observation as assessed by primary MSK care provider

• Willing and able to sign an informed consent document

Locations
United States
New York
Memorial Sloan Kettering Cancer Center
RECRUITING
New York
Contact Information
Primary
Aimee M Crago, MD, PhD
cragoa@mskcc.org
212-639-4807
Backup
Meera Hameed, MBBS
hameedm@mskcc.org
212-639-7959
Time Frame
Start Date: 2020-02-19
Estimated Completion Date: 2026-02-19
Participants
Target number of participants: 100
Treatments
Desmoid Fibromatosis
Participants will have a clinical diagnosis of desmoid fibromatosis, either new or newly recurrent
Related Therapeutic Areas
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov

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