Systemic Lupus, Skin Lupus Clinical Trial
— LUPOBSOfficial title:
Lupus and Observance
| NCT number | NCT03019926 |
| Other study ID # | 16/B/09 |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | January 19, 2017 |
| Est. completion date | July 19, 2018 |
| Verified date | June 2018 |
| Source | University Hospital Center of Martinique |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
A poor therapeutic observance is described between 3 and 76% cases in systemic lupus. It is
associated with an increased risk of relapses, hospitalizations, morbidity and poor renal
prognosis.
New treatment protocols exist and are indicated in second intention in case of good
compliance. An assessment of therapeutic adherence is therefore essential.
Patients with systemic lupus diagnosed for at least 6 months, or skin lupus, who have been
prescribed with Plaquenil (hydroxychloroquine), will be included in the study.
The study primary objective is to determine risk factors for non-observance
The secondary objectives are to:
- Measure the observance rate of patients with systemic lupus in Martinique.
- Describe the parameters that influence observance: evaluation of the disease and
associated comorbidities, psychosocial assessment, assessment of the doctor-patient
relationship, evaluation of the disease representations.
| Status | Completed |
| Enrollment | 200 |
| Est. completion date | July 19, 2018 |
| Est. primary completion date | July 19, 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: 1. Age = 18 years 2. Systemic lupus defined according to the diagnostic criteria of the American College of Rheumatology " 1997, diagnosed for at least 6 months; Or Skin Lupus 3. Consultation or hospitalization at the University Hospital of Martinique, in either services of Internal Medicine, Rheumatology or Dermatology. 4. Prescription of hydroxychloroquine (Plaquenil®) for at least 6 months 5. Affiliate or beneficiary of a social security scheme. 6. Patient not opposed to participate in the study Exclusion Criteria: 1. Age <18 years or patient under guardianship 2. Patient not speaking and / or not understanding French 3. No prescription and/or contraindication to hydroxychloroquine 4. Systemic lupus outbreak with neurological impairment defined by SLEDAI score by a psychosis (disruption of normal activity in relation to a severe alteration of the perception of reality. Includes: hallucinations, incoherence, impoverishment of the content of thought, illogical reasoning, bizarre behavior, disorganized or catatonic) or brain damage (with impairment of mental functions with impaired orientation, memory or other brutal appearance and fluctuating evolution). 5. History of psychiatric disorders: personality disorders, psychoses, severe depression 6. Hospitalization with a life-threatening clinical condition that does not allow to answer questions 7. Non affiliated patient or beneficiary of a social security scheme. 8. Patient refusing to participate in the study |
| Country | Name | City | State |
|---|---|---|---|
| France | CHU de Martinique | Fort-de-France | Martinique |
| Lead Sponsor | Collaborator |
|---|---|
| University Hospital Center of Martinique |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The primary outcome measure is based on a blood dosage of hydroxychloroquine (HCQ) | The HCQ dosage is assayed on whole blood (6ml) by high-pressure liquid chromatography performance, reproducible and inexpensive method. Only one laboratory centralizes the sampling. A dosage below 200 ng/ml or 0.2 mg/l defines a non-observing patient within the 40 days above. |
Reflects the Plaquenil intake during the 40 previous days | |
| Secondary | Patients considered as observing and non-observing will be compared according to the activity of the disease | Activity of the disease : Systemic lupus considered as active for a SELENA-SLEDAI score = 6 | 40 days | |
| Secondary | Patients considered as observing and non-observing will be compared according to number of prescribed medication | 40 days | ||
| Secondary | Patients considered as observing and non-observing will be compared according to the presence of anxiety and/or depressive disorders | Presence of anxiety and/or depressive disorders, according to the Hospital Anxiety And Depression Scale (HAD), a score > to 10 | 40 days |