Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07005479

Long-Term Outcomes in SLE at Peking University People's Hospital

This study aims to prospectively follow patients diagnosed with Systemic Lupus Erythematosus (SLE) at Peking University People's Hospital, assessing long-term outcomes such as disease activity, organ involvement, survival, and quality of life. Findings will support individualized patient management and contribute to understanding disease progression in the Chinese population.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Rheumatology and Immunology, Peking University People's Hospital

Beijing, Beijing Municipality, 100044, China

Location status: Recruiting

Location contact

Haihong Yao, MD

CONTACT

[email protected]

010-88326666

About this study

This single-center, prospective observational cohort study aims to evaluate the long-term clinical outcomes of patients diagnosed with SLE at Peking University People's Hospital. SLE is a chronic, heterogeneous autoimmune disease that can lead to cumulative organ damage, impaired quality of life, and premature mortality. Although disease control has improved with the advent of immunosuppressive therapies, predicting long-term outcomes remains a challenge.

The study will enroll adult SLE patients and follow them for a period of up to 10 years. Data will be collected at regular intervals, including clinical assessments, laboratory findings, treatment history, and patient-reported outcomes. A particular focus will be placed on measuring disease activity using validated indices such as the SLE Disease Activity Index (SLEDAI) and on evaluating the achievement and maintenance of Lupus Low Disease Activity State (LLDAS).

LLDAS is a validated treat-to-target goal associated with reduced damage accrual and improved prognosis. It will be assessed at each follow-up visit based on established criteria, including low disease activity (SLEDAI-2K ≤4 with no major organ activity), no new disease activity, low-dose glucocorticoid use (prednisone ≤7.5 mg/day or equivalent), and stable standard immunosuppressants. The frequency, duration, and determinants of achieving and sustaining LLDAS over time will be analyzed as a key outcome, alongside major organ involvement, flare rates, survival, and quality of life.

This study will provide real-world data on long-term disease trajectories in a Chinese tertiary hospital population and offer insights into predictors of favorable outcomes, guiding personalized disease management strategies and supporting the implementation of treat-to-target approaches in clinical practice.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All patients must meet at least one of the following classification criteria for Systemic Lupus Erythematosus (SLE):

The 1997 American College of Rheumatology (ACR) Revised Classification Criteria; The 2012 Systemic Lupus International Collaborating Clinics (SLICC) Classification Criteria; The 2019 EULAR/ACR Classification Criteria for SLE. 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. Proportion of Patients Achieving and Sustaining Lupus Low Disease Activity State (LLDAS)

    Time frame: Approximately 5-10 years

    LLDAS is defined according to the Asia Pacific Lupus Collaboration (APLC) criteria as meeting all of the following at a study visit:

    SLEDAI-2K ≤4 with no activity in major organ systems (renal, CNS, cardiopulmonary, vasculitis, etc.)

    No new features of lupus disease activity compared to the previous assessment

    Physician Global Assessment (PGA) ≤1 (on a 0-3 scale)

    Prednisone (or equivalent) dose ≤7.5 mg/day

    Use of standard maintenance immunosuppressive drugs only

Secondary outcomes

  1. Organ Damage Accrual Measured by the SLICC/ACR Damage Index (SDI)

    Time frame: Annually over a 10-year follow-up period

    Organ damage will be assessed using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). SDI ranges from 0 to 47, with higher scores indicating more severe, irreversible organ damage accrued since the onset of SLE. A score of 0 indicates no damage, while each additional point reflects cumulative damage in different organ systems.

  2. Lupus-Related Mortality Rate

    Time frame: Approximately 5-10 years

    Number and proportion of deaths directly attributable to SLE or its complications (e.g., infection, renal failure, cardiovascular events).

  3. Glucocorticoid-Sparing Effect

    Time frame: Assessed at each follow-up visit (up to 10 years)

    Proportion of patients achieving and maintaining prednisone (or equivalent) ≤7.5 mg/day without disease flare. Also evaluating cumulative steroid dose over time.

Study contacts

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

Haihong Yao, MD

CONTACT

[email protected]

010-88326666

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Registry information

Official study title

A Prospective Cohort Study on Long-Term Outcomes in Patients With Systemic Lupus Erythematosus at Peking University People's Hospital

Acronym: LOTUS

Important dates

Study start
2020
Primary completion
2030
Study completion
2032
First posted
Jun 5, 2025
Registry last updated
Jun 5, 2025

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.