Treatment group will receive 1500 mg/day (three 500 mg tablets/day) of ß-D mannuronic acid orally for 12 weeks.
Sponsors
Vice-Chancellor for Research, Tehran University of Medical Sciences
Conditions
Ankylosing spondylitis.
Ankylosing spondylitisRheumatoid Arthritis.
Seropositive Rheumatoid Arthritis
Phase 2
The therapeutic effects of ß-D-Mannuronic acid in patients with ankylosing spondylitis
Active, not recruitingIRCT2013062213739N1
Start: 2014-04-20Target: 35Updated: 2018-02-22
The therapeutic effects of ß-D-Mannuronic acid in patients with Rheumatoid Arthritis
Active, not recruitingIRCT2014011213739N2
Start: 2014-07-20Target: 35Updated: 2018-02-22