The Treat-to-target Study of RA Based on Smart System of Disease Management(SSDM)

NCT03715595 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2200

Last updated 2020-06-05

No results posted yet for this study

Summary

This study evaluate the Smart System of Disease Management(SSDM)to improve the treat-to-target(T2T) and the safety of drug in the treatment of rheumatoid(RA). All participants will be randomized in the SSDM group and the control group. The patients in the SSDM group will use the SSDM every month and the control group will receive the conventional therapy.

Conditions

Interventions

OTHER

SSDM group

The patients can perform self-evaluation, including DAS28, morning stiffness duration (MSD) and HAQ, and input medical records (including medication and laboratory test results) every month.

Sponsors & Collaborators

  • Anhui Provincial Hospital

    collaborator OTHER_GOV
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Peking University International Hospital

    collaborator OTHER
  • Xuanwu Hospital, Beijing

    collaborator OTHER
  • Dongguan donghua hospital

    collaborator UNKNOWN
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • Hebei General Hospital

    collaborator OTHER
  • Bethune International Peace Hospital

    collaborator OTHER
  • Central South University

    collaborator OTHER
  • The First Affiliated Hospital with Nanjing Medical University

    collaborator OTHER
  • Subei People's Hospital of Jiangsu Province

    collaborator OTHER
  • The First Affiliated Hospital of BaoTou Medical College

    collaborator OTHER
  • Linyi People's Hospital

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Mianyang Central Hospital

    collaborator OTHER
  • Tianjin Medical University General Hospital

    collaborator OTHER
  • The First People's Hospital of Yunnan

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    collaborator OTHER
  • Zhejiang Provincial People's Hospital

    collaborator OTHER
  • First Hospital of China Medical University

    collaborator OTHER
  • Xijing Hospital

    collaborator OTHER
  • Tianjin First Central Hospital

    collaborator OTHER
  • Peking University People's Hospital

    lead OTHER

Principal Investigators

  • Chun Li, doctor · Peking University People's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-01
Primary Completion
2020-05-29
Completion
2020-06-29

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03715595 on ClinicalTrials.gov