Cure Cystinosis International Registry

Cystinosis Clinical Trial

— CCIR  

Official title:

Cure Cystinosis International Registry

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01327807
• Other study ID #: CCIR100913
• Status: Recruiting
• Phase: N/A
• First received: March 29, 2011
• Last updated: March 10, 2014
• Start date: August 2010
• Est. completion date: December 2022

Study information

• Verified date: March 2014
• Source: Cystinosis Research Foundation
• Contact: Betty L Cabrera, M.P.H
• Phone: 858-822-3747
• Email: curator[@]cystinosisregistry.org
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Cure Cystinosis International Registry (CCIR) is an online, patient self-identifying registry developed by medical and scientific experts specifically for the cystinosis community.

CCIR's sole purpose is to identify people with cystinosis worldwide in an effort to accelerate novel treatments and a cure for cystinosis.

CCIR provides a safe and secure platform for:

• sharing anonymous medical information about cystinosis with researchers, clinicians and patients

• disseminating information about research opportunities

• connecting researchers/investigators and prospective participants *

Interested cystinosis patients may register themselves with CCIR online at http://www.cystinosisregistry.org.

• No personal information is shared outside of CCIR. Individual identities are known only to appropriate CCIR staff. If a participant is matched to a clinical trial, the participant receives a notice from CCIR, after which they can decide whether they wish to contact the study sponsor.

Description:

Significance and Purpose:

Many different resources and tools are necessary to make significant advances in medical research. Progress in rare diseases such as cystinosis can often be impeded by the lack of information available about the disease and limited access to volunteers eligible for clinical trials. Therefore, patients who are willing to provide information about how the disease has affected them and also make themselves available to participate in trials are among the most valuable resources the investigators have to fight a disease. However, the research community desperately needs the right tool that will permit access to these resources.

A tool widely used to conveniently collect both data about a disease and information about potential clinical trial participants is a patient registry. A patient registry is any system that allows for the organized collection of data about disease outcomes in affected populations for a scientific, clinical, or policy purpose. The Cystinosis Research Foundation (CRF) has aligned itself with cystinosis medical experts and organizations worldwide to create the first ever international, online patient registry for cystinosis, Cure Cystinosis International Registry (CCIR). The express purpose of CCIR is to make anonymous information available to the research community and thus promote accelerated research in advanced treatments and ultimately a cure for cystinosis.

Objectives:

The objectives of CCIR are:

• Evaluate epidemiology and clinical characteristics of cystinosis around the world.

• Evaluate and compare the diagnosis, treatment, and kidney transplant rates among cystinosis communities from different geographical areas.

• Enhance the understanding of how cystinosis affects quality of life.

CCIR Registration:

Interested cystinosis patients may register themselves with CCIR online at http://www.cystinosisregistry.org. Registration is easy and secure. Simply go to the website and create a CCIR account and complete a survey. The CCIR website is currently available in English and Spanish, and will soon be available in French, Portuguese, and possibly other languages.

Benefits to CCIR participants include instant access to the registry's accumulated survey results (reported as anonymous group data), and opportunities to submit questions to cystinosis experts and to learn of clinical trial opportunities. No personal information is shared outside of CCIR. Individual identities are known only to appropriate CCIR staff.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 750
• Est. completion date: December 2022
• Est. primary completion date: December 2020
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Diagnosis of cystinosis

Study Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Cystinosis
• Fanconi Anemia
• Fanconi Syndrome
• Nephropathic Cystinosis
• Renal Fanconi Syndrome

Locations

Country	Name	City	State
United States	University of California, San Diego	San Diego	California

Sponsors (1)

Lead Sponsor	Collaborator
Cystinosis Research Foundation

Country where clinical trial is conducted

United States, 

References & Publications (2)

Cherqui S. Cysteamine therapy: a treatment for cystinosis, not a cure. Kidney Int. 2012 Jan;81(2):127-9. doi: 10.1038/ki.2011.301. — View Citation

Gangoiti JA, Fidler M, Cabrera BL, Schneider JA, Barshop BA, Dohil R. Pharmacokinetics of enteric-coated cysteamine bitartrate in healthy adults: a pilot study. Br J Clin Pharmacol. 2010 Sep;70(3):376-82. doi: 10.1111/j.1365-2125.2010.03721.x. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Age at treatment initiation and the effect on disease outcomes		Lifetime	No

External Links

•   CCIR Patient Portal
•   Cystinosis Research Foundation