Rheumatoid Arthritis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- (Nomogram group) You do not have any dry mouth or dry eye symptoms.
- (Sicca group) You are already receiving a salivary gland scan (a test called sialoscintigraphy) as part of your care.
Who may not be able to join:
- You are currently pregnant.
- You are currently breastfeeding.
- You have HIV.
- You have cancer and are currently receiving treatment for it.
- (Nomogram group) You have a long-term illness that requires regular medical check-ups.
- (Nomogram group) You are taking antihistamines, water pills (diuretics), antidepressants, psychiatric medications, anti-anxiety medications, or anti-inflammatory painkillers (such as ibuprofen) that may affect saliva production.
- (Nomogram group) You have smoked within the last year.
- (Nomogram group) You have tested positive for certain antibodies related to autoimmune conditions (anti-SSA or anti-ENA) (confirm with trial site).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: National Taiwan University Hospital, National Taiwan University Hospital
Phone: 0972652625
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Quantitative profiles of sialoscintigraphy, including accumulation velocity and secretion velocity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.