Scleroderma Registry & Repository At the Hospital for Special Surgery

Hospital for Special Surgery (HSS)

Status

Enrolling

Conditions

Scleroderma

Study type

Observational

Funder types

Other

Identifiers

NCT01656447

2014-276

Details and patient eligibility

About

The overall objective of the Scleroderma Registry is to support and promote the basic science and clinical research of this complex rheumatic disease at the Hospital for Special Surgery (HSS). The registry facilitates our understanding of the clinical features, pathobiology, genetics of Scleroderma. This will ultimately lead to a potential treatment for this currently untreatable condition.

Full description

What will be asked of you:

Completion of 2 health questionnaires
Donation of research bloods. This is optional, but encouraged (if possible).
We also encourage patients who come for initial visits to return so follow-up data can be collected.

Benefits to Patients:

The HSS Scleroderma Registry gives patients the opportunity to participate in observational research with the goal of improving the lives of patients in the future.
By donating research bloods and providing clinical information, patients will help generate new knowledge about Scleroderma that can guide the treatment and care of patients afflicted with this rare disease.
Patients will also receive a comprehensive, medical evaluation from an HSS physician who specializes in treating Scleroderma. He or she will provide guidance on treatment options and recommendations for current or upcoming clinical trials.
Physicians will also make patients aware of the resources available to them, including support groups and educational programs.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria