Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Interstitial Lung Disease
  • Primary Sjögren's Syndrome
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 75 years
Gender
Both males and females

Description

This study will be a randomized, double-blind, positive control clinical trial with a course of 24 weeks. Random scheme:the DAS for Interactive Web Response System(IWRS) will be used to calculate and distribute random numbers and dispensing drugs. Blind method ?The test process will be in a double-b...

This study will be a randomized, double-blind, positive control clinical trial with a course of 24 weeks. Random scheme:the DAS for Interactive Web Response System(IWRS) will be used to calculate and distribute random numbers and dispensing drugs. Blind method ?The test process will be in a double-blind state. Control drug: The lung rehabilitation training will be used as control in this trial.

Tracking Information

NCT #
NCT04544722
Collaborators
Not Provided
Investigators
Principal Investigator: Zhujing Zhu, Ph.D Longhua Hospital Study Chair: Jianchun Mao, Master Longhua Hospital Study Chair: Huanru Qu, Ph.D Longhua Hospital