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Clinical Trials in China / NCT06730334
Recruiting Observational

Prospective Study of Classification and Activity Assessment of Psoriatic Arthritis Based on Power Doppler (PD) Ultrasonography (PDUS)

NCT06730334 · tracked via the Priya Life Science China tracker
Sponsor
Nanjing Medical University
Phase
Observational
Started
2023-09-01
Last updated
2024-12-20

Condition(s) studied

Psoriatic ArthritisSecukinumabUltrasonography

Study summary

Psoriatic arthritis (PsA) is a complex inflammatory disease with heterogeneous clinical features, which complicates psoriasis in 30% of patients. PsA involves multiple tissues and clinical domains including skins and nails as well as arthritis, spondylitis, enthesitis, and dactylitis. Power Doppler (PD) ultrasonography (PDUS) is a sensitive non-invasive imaging technology used to assess disease activity and treatment response in PsA. This is a prospective, observational, open-label study to investigate disease activity, therapeutic response and bone destruction based on ultrasonography findings in patients with PsA.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * PsA patients as defined by CASPAR criteria * Patients must be able to comply with the visit schedule, treatment plan, laboratory tests and other study procedures * Patients must be given informed consent Exclusion Criteria: * History of other arthritis within the last 12 months * Concomitant disease with acute or chronic infectious diseases * Pregnancy or laction * Poorly tolerated with venipuncture required for blood sampling during the study

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Department of Rheumatology and Immunology, Jiangsu Province Hospital Nanjing Jiangsu Recruiting
Jiangsu Province Hospital Nanjing Jiangsu Recruiting

More Nanjing Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06730334 on ClinicalTrials.gov ↗ ← All trials in China