NCT Number: NCT00004288
Phase II Pilot Study of Olsalazine for Ankylosing Spondylitis
OBJECTIVES:
I. Assess the safety and efficacy of olsalazine, a dimer of 5-aminosalicylic acid, in men with ankylosing spondylitis unresponsive to nonsteroidal anti-inflammatory drugs and physiotherapy.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 2
About this study
PROTOCOL OUTLINE: Patients are treated with daily olsalazine. The dose is increased each week until the protocol dose is reached.
Supplemental acetaminophen is allowed; nonsteroidal anti-inflammatory drugs continue unchanged. Concurrent sulfasalazine is prohibited.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
- Meets modified New York diagnostic criteria
- Active disease, i.e., morning stiffness for more than 30 minutes
- Failed or experienced nonlife-threatening reaction to prior sulfasalazine
- No significant hematologic, hepatic, or renal disease
Treatment and study plan
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Lead sponsor
National Center for Research Resources (NCRR)
Nih
Collaborators
- University of Rochester
Registry information
Important dates
- Study start
- 1996
- Study completion
- 1999
- First posted
- Oct 19, 1999
- Registry last updated
- Jun 24, 2005
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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