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Insufficient accrual. Recruitment was stopped because enrollment targets were unlikely to be achieved. A total of 505 of 600 planned participants were enrolled. Data will be included in planned pooled analyses.
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Biopsies are performed in several autoimmune diseases to diagnose or classify them Tolerance and information of the patients have been poorly evlauated our objective is to evaluate tolerance and information of the patients after the biopsies for salivary gland, temporal arteries and neuromuscular.
patinets that benefited of arterial temporal biospy or salivary gland biospy or muscuar biopsy or neuro muscular biospy for his auto -mmune disease will be included and fill standardized questionnaires concerning tolerance, information and side effect at inclusion , day 7 and day 30 after the biopsy data will be analysed to evaluate information, tolerance and risk factor af side effect
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Salivary gland biospy, | 100 Salivary gland biospy use for the diagnosis of sjogern disease or other auto-immune disease. | ||
| muscular biopsy, | muscular biospy use for the diagnosis of muscular auto-immune disease. | ||
| neuro muscular biospy | neuro muscular biospy use for the diagnosis of vasculitis,muscular auto-immune disease or neuro-muscumar auto-immune disease | ||
| temporal arteries biospy | temporal arteries biospy uses for the diagnosis of giant cell arteritis |
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| Measure | Description | Time Frame |
|---|---|---|
| tolerance of each type of biopsy | tolerance based on a standardized patient 's questionnaire | tolerance at day 7 after the biospy was performed |
| Measure | Description | Time Frame |
|---|---|---|
| tolerance of each type of biopsy 30 days after | tolerance based on a standardized patient 's questionnaire | tolerance at day 30 and at inclusion after the biospy was performed |
| evaluation of the qualitiy of patient's information at inclusion |
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Inclusion Criteria:
Exclusion Criteria:
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all patients that underwent a biospy for his auto-immune rare disease
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU d'ANGERS | Angers | France | ||||
| CHU de Bordeaux |
All collected data that underlie results in a publication
Data will be available beginning one year and ending five years following the publication
Data access requests will be reviewed by the internal committee of Brest UH. Requestors will be required to sign and complete a data access agreement.
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standardized questionnaire at inclusion
| questionnaire at inclusion |
| risk factor of sied effect of each biospy | standardized questionnaire | standardized questionnaire at inclusion, day 7 and 30 |
| Bordeaux |
| 33000 |
| France |
| CHRU de Brest | Brest | 29609 | France |
| CHU de LILLE | Lille | 59037 | France |
| CHU de Marseille | Marseille | France |
| Hôpital de la Salpétrière | Paris | 75013 | France |
| CH de Quimper | Quimper | 20007 | France |
| CHU de Tours | Tours | France |