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Validation of the Lupus Low Disease Activity State (LLDAS) in the Asia Pacific Region

Validation of the Lupus Low Disease Activity State (LLDAS) in the Asia Pacific Region

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03138941
Acronym
APLCLLDAS
Enrollment
5000
Registered
2017-05-03
Start date
2013-09-01
Completion date
2032-12-31
Last updated
2024-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic Lupus Erythematosus

Brief summary

Lupus Low Disease Activity State (LLDAS) study is an international, multi-centre prospective study, developed by the Asia Pacific Lupus Collaboration (APLC) to investigate whether the attainment of LLDAS is associated with improved outcomes in patients with Systemic Lupus Erythematosus (SLE). SLE, or lupus, is the archetypal multisystem autoimmune disease, with an estimated incidence of 5-50 cases per 100,000 people. Patients with SLE, usually young women, suffer a marked loss of life expectancy, and severe morbidity, due to a heterogeneous range of clinical manifestations caused by autoimmune-mediated inflammation of multiple organs. The most severe manifestations of SLE are the accrual of irreversible organ damage, especially renal and central nervous system (CNS) involvement. As there is no effective targeted monotherapy for SLE, patients also suffer severe toxicity from the use of glucocorticoids and broad-spectrum immunosuppressive therapies. Despite combination therapy with current drugs, many studies show that the majority of patients suffer inadequate disease control and inexorably accrue permanent organ damage over time. The diversity of clinical features of active SLE has made quantification of disease activity problematic. Although there are a number of published systems in use to measure SLE disease activity, there are widely acknowledged problems with these instruments. Published definitions of remission are so stringent that they are met by less than 5% of patients. This lead to the realisation that rather than lupus remission, a lupus low disease activity state target may be more feasible, and that patients with low disease activity are more homogeneous than patients with active disease. Thus, the development of a definition of lupus low disease activity, which is feasible and has face validity, escapes the complexity of attempts to quantify heterogeneous states of active disease. In this study, the investigators will prospectively collect longitudinal data on consecutive SLE patients at each centre to evaluate the LLDAS definition. Protection from organ damage accrual as the primary endpoint.

Detailed description

In this study, patients with SLE will be followed for \ 5 years. Regular recordings of the data needed to score LLDAS (disease activity and treatment domains, see Franklyn L et al, Ann Rheum Dis 2016) will be collected, as well as annual recording of lupus-related damage using the SLICC\_ACR Damage Index (SDI) and quality of life using the Short Form 36 version 2 (SF36v2). At conclusion of primary data collection, the associate of LLDAS attainment, or sustained attainment, with protection from organ damage accrual will be ascertained.

Interventions

None listed

Sponsors

Flinders Medical Centre, Adelaide, AUSTRALIA
CollaboratorUNKNOWN
St. Vincent's Hospital, Melbourne, AUSTRALIA
CollaboratorUNKNOWN
Royal Adelaide Hospital, Adelaide, AUSTRALIA
CollaboratorUNKNOWN
University of New South Wales, Sydney, AUSTRALIA
CollaboratorUNKNOWN
People's Hospital, Peking University Health Science Center, Beijing, CHINA
CollaboratorUNKNOWN
Peking University First Hospital, Beijing, CHINA
CollaboratorUNKNOWN
The University of Hong Kong
CollaboratorOTHER
University of Padjadjaran, Bandung, INDONESIA
CollaboratorUNKNOWN
Tokyo Women's Medical University, JAPAN
CollaboratorUNKNOWN
University of Occupational and Environmental Health, JAPAN
CollaboratorUNKNOWN
Keio University, JAPAN
CollaboratorUNKNOWN
Hanyang University Hospital for Rheumatic Diseases, REPUBLIC OF KOREA
CollaboratorUNKNOWN
University of Santo Tomas Hospital, Philippines
CollaboratorOTHER
National University Hospital, Singapore
CollaboratorOTHER
Tan Tock Seng Hospital
CollaboratorOTHER
Chang Gung Memorial Hospital
CollaboratorOTHER
Taichung Veterans General Hospital
CollaboratorOTHER
Chiang Mai University Hospital, THAILAND
CollaboratorUNKNOWN
Middlemore Hospital, New Zealand
CollaboratorOTHER
North Shore Hospital, Auckland, NEW ZEALAND
CollaboratorUNKNOWN
Auckland District Health Board, Auckland, NEW ZEALAND
CollaboratorUNKNOWN
Teaching Hospital Kandy, SRI LANKA
CollaboratorUNKNOWN
University of the Philippines, Philippines
CollaboratorUNKNOWN
Monash University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients have to meet either the 1997 American College of Rheumatology (ACR) Modified Classification Criteria for SLE, with at least four of the 11 items; or alternatively, fulfil the Systemic Lupus International Collaborating Clinics (SLICC) 2012 Classification Criteria, with at least four of the 17 items (at least one clinical and one immunological criterion) or with lupus nephritis in the presence of at least one immunological criteria. Patients can be either newly diagnosed or longstanding lupus patients. All patients must be over the age of 18 and competent to provide written consent.

Exclusion criteria

* Patients less than 18 years of age and patients who are unable to consent are excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
SLICC-ACR Damage IndexApproximately 5-10 yearsOrgan damage accrual

Secondary

MeasureTime frameDescription
SFv2-36Approximately 5-10 yearsQuality of Life
MortalityApproximately 5-10 yearsMortality

Countries

Australia, China, Hong Kong, Indonesia, Japan, Philippines, Singapore, South Korea, Sri Lanka, Taiwan, Thailand

Contacts

Primary ContactEric F Morand
eric.morand@monash.edu+ 61 3 8572 2650
Backup ContactRangi K KANDANE-RATHNAYAKE
Rangi.Kandane-Rathnayake@monash.edu+ 61 3 8572 2561

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026