CorEvitas, LLC
Waltham, Massachusetts, 02451, United States
Location status: Recruiting
NCT Number: NCT06100991
Prospective, observational registry for subjects with GPP under the care of a dermatology investigator.Approximately 200 subjects and 75 clinical sites in North America will be recruited to participate with no defined upper limit for either target
Interested in participating?
Request Info18 year and older
All sexes
Observational
Waltham, Massachusetts, 02451, United States
Location status: Recruiting
The objective of the registry is to obtain information on the treatment patterns, disease activity progression, and the development of comorbidities and adverse events in a cohort of patients with GPP. Data collected will be used to better characterize the natural history and longitudinal trajectory of the disease. This will be done through the standardized data collection including validated patient-reported outcomes (PRO) and clinician-reported outcomes (ClinRO), the active evaluation of prevalent and incident comorbidities and adverse events, and the recording of medication utilization patterns. Personal information is also collected from each consenting registry subject allowing for linkages to other public or private clinical and administrative databases, as well as to databases maintained by organizations focused on the care and treatment of GPP for the purposes of clinical, market, or outcomes research.
This provides an opportunity to evaluate other aspects of the disease and its treatment, including but not limited to clinical and drug cost-effectiveness, health care resource utilization, and subject adherence.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Through study completion, an average of 10 years
The major clinical outcomes include an assessment of the epidemiology of GPP; to better understand the presentation and natural history.
Time frame: Through study completion, an average of 10 years
The major clinical outcome include an assessment of the epidemiology of GPP; to better understand the management and outcomes.
Contact information is provided by the study sponsor or research team.
CorEvitas
Network
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06477536
Generalized Pustular Psoriasis, Psoriasis
Beijing, China
View Trial DetailsNCT06295692
Erythrodermic Psoriasis, Generalized Pustular Psoriasis
Hokkaido, Japan
View Trial DetailsNCT06323356
Erythrodermic Psoriasis, Generalized Pustular Psoriasis
Nagoya, Aichi-ken, Japan
View Trial DetailsNCT06013969
Generalized Pustular Psoriasis, Psoriasis
Irvine, California, United States
View Trial Details