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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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data 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