Taking peoplePhase 3
QUIDOSE. Randomized controlled trial testing the efficacy of hydroxychloroquine combined with low dose corticosteroid therapy in pulmonary sarcoidosis
Key facts
- Who runs it
- Assistance Publique Hopitaux De Paris
- Where
- France32 sites in 1 countryChoose a country to see its sites
- Status
- Recruiting
- Phase
- Phase 3
- People taking part
- 170 people, planned
- Started
- 28 Oct 2024
- Expected to end
- 30 Jun 2029
- Type of study
- Interventional
- Record updated
- 7 August 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 25 criteriaShow less
Who can take part
- Aged ≥18 and ≤80 years
- Pulmonary sarcoidosis meeting ATS 2020 AJRCCM diagnostic criteria ( (i) compatible presentation, (ii) non-necrotizing granuloma in one or more tissues, exclusion of alternative granulomatous diseases)
- Patient presenting : - Lung activity on imaging (e.g., micronodules, nodules, ground glass, consolidations, septal lines) - And FVC ≤ 80% pred and/or ≥10% absolute decline in FVC from the best FVC or FVC ≤ 90% pred with significant physical performance deterioration in the last year - And one or more respiratory symptom(s) among the following: cough, dyspnea, chest pain
- Effective contraception for women of childbearing potential until 8 months post-treatment
- Informed and signed consent
- Social security coverage
Who cannot take part
- Systemic corticosteroid or immunosuppressant use for at least 7 days in the previous 3 months inclusion/randomization
- Participation in another interventional therapeutic trial within 6 months before inclusion
- Severe sarcoidosis requiring immediate and urgent results and/or high-dose corticosteroids (severe/active neurological (except facial nerve involvement), cardiac, ophthalmic (except local treatment-responsive form), laryngeal, renal involvement, severe hypercalcemia, severe hepatic)
- HIV positivity, active Hepatitis B or C
- History of hydroxychloroquine treatment for sarcoidosis
- Cardiomyopathy with heart failure
- Other conditions affecting respiratory function: moderate to very severe COPD, uncontrolled asthma, obesity (BMI >30), fibrotic pulmonary disease, pulmonary neoplasia
- History of retinopathy or maculopathy
- Corticosteroid contraindications (hypersensitivity, infections, evolving virosis, glaucoma, uncontrolled psychosis, live vaccines, uncontrolled diabetes, uncontrolled hypertension)
- Glucose-6-Phosphate Dehydrogenase deficiency (acute hemodialysis risk)
- Hydroxychloroquine contraindications (hypersensitivity, severe retinal or cataract, unilateral blindness, myasthenia gravis, QTc prolongation, concurrent QT-prolonging drugs)
- Renal insufficiency with clearance <60ml/min
- Current pregnancy
- Breastfeeding
- Inability to respond to questionnaires despite aid
- Patient under guardianship or curatorship
- Patient under judicial protection
- Tamoxifen use
- Acute porphyria risk
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
About the trial
What the trial wants to find out
To demonstrate the non-inferiority of hydroxychloroquine combined with low-dose corticosteroids versus medium-dose corticosteroid therapy in improving respiratory function at 6 months
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
- Official title
- QUIDOSE. Randomized controlled trial testing the efficacy of hydroxychloroquine combined with low dose corticosteroid therapy in pulmonary sarcoidosis.
- Record updated
- 7 August 2026