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Spots Global Cancer Trial Database for trūFreeze® Spray Cryotherapy Patient Registry

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Trial Identification

Brief Title: trūFreeze® Spray Cryotherapy Patient Registry

Official Title: trūFreeze® Spray Cryotherapy Patient Registry

Study ID: NCT01802203

Study Description

Brief Summary: To collect efficacy and outcomes data related to the use of trūFreeze® spray cryotherapy for the treatment of unwanted tissue in the pulmonary and gastrointestinal settings.

Detailed Description: This is a prospective, multi-center registry of patients who are currently undergoing spray cryotherapy using the trūFreeze® device. The registry population consists of patients who are being treated using the spray cryotherapy trūFreeze® device for the removal of unwanted tissue, such as malignant or pre-malignant conditions in the pulmonary or gastrointestinal settings. Patients eligible to participate in the registry will have disease and treatment specific data collected throughout therapy and long-term follow-up. Subjects will be considered to have completed the registry when data from the 5 year follow-up visit has been collected. The beginning of the follow-up period commences with the first endoscopic treatment session. Subjects may be withdrawn prior to this for any of the following reasons: 1. Death, or 2. Lost to Follow-Up, or 3. Withdrawal of consent, or 4. Discontinuation by the investigator. Three attempts at contact using two different methods are required prior to determination that the subject is lost to follow-up. Attempts at contact must be with certified letters OR documented telephone contact. The registry will utilize electronic case report forms using a web-based platform housed at the University of North Carolina at Chapel Hill. Access to the database will be limited to individuals involved in the research registry and will require a unique user ID and password. All access to the database and web-based application will be encrypted (HTTPS) and electronic systems compliant with applicable privacy and security regulations. To maintain patient confidentiality, all subjects will be assigned a registry identification number, and this will be the only link between subject identity and treatment information. Read-only access will be provided to any personnel who is not an administrator or responsible for data entry. All data requested on the case report form must be recorded. All missing data must be explained. The system allows sites to directly enter data electronically, however sites are still responsible for ensuring they have source documents that support all data entered electronically that are separate and verifiable. The registry system will maintain an audit trail that captures when electronic entries are changed, what the change was, and who made the change. The investigators will ensure the capability for inspections of applicable registry-related facilities (e.g. pharmacy, diagnostic laboratory, etc.). The registry will be monitored by the sponsor, and allow auditing by the Institutional Review Board, government regulatory bodies, and University compliance and quality assurance groups of all registry related documents (e.g. source documents, regulatory documents, data collection instruments, registry data, etc.).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Scripps Green Hosptial, La Jolla, California, United States

University of Colorado Denver, Denver, Colorado, United States

Borland-Groover Clinic, Jacksonville, Florida, United States

Ochsner Medical Center, Kenner, Louisiana, United States

University of Maryland, Baltimore, Maryland, United States

Walter Reed National Military Medical Center, Bethesda, Maryland, United States

Massachusetts General Hosptial, Boston, Massachusetts, United States

Boston University Medical Center, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

ProHEALTH Care Associates, Lake Success, New York, United States

NYU, New York, New York, United States

University of Rochester/Strong Memorial Medical Center, Rochester, New York, United States

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

Ahuja Medical Center-CWR University Hosptials, Beachwood, Ohio, United States

Rhode Island Hospital, Providence, Rhode Island, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Contact Details

Name: Nicholas Shaheen, MD

Affiliation: University of North Carolina, Chapel Hill

Role: PRINCIPAL_INVESTIGATOR

Name: Robert F Browning, MD

Affiliation: Walter Reed National Military Medical Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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