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NCT Number: NCT03138941

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Rheumatology, Flinders Medical Centre, Adelaide, South Australia, Australia

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. SLICC-ACR Damage Index

    Time frame: Approximately 5-10 years

    Organ damage accrual

Secondary outcomes

  1. SFv2-36

    Time frame: Approximately 5-10 years

    Quality of Life

  2. Mortality

    Time frame: Approximately 5-10 years

    Mortality

Study contacts

Contact information is provided by the study sponsor or research team.

Eric F Morand

CONTACT

[email protected]

+ 61 3 8572 2650

Rangi K KANDANE-RATHNAYAKE

CONTACT

[email protected]

+ 61 3 8572 2561

Sponsors and collaborators

Lead sponsor

Monash University

Other

Collaborators

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

Registry information

Acronym: APLCLLDAS

Important dates

Study start
2013
Primary completion
2027
Study completion
2032
First posted
May 3, 2017
Registry last updated
Dec 12, 2024

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.

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