Actively Recruiting
Parathyroid Assessment of Symptoms French Version
Led by Nantes University Hospital · Updated on 2026-05-04
548
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Primary hyperparathyroidism has been associated with an impaired quality of life. Surgery has been suggested to improve this outcome in patients with baseline quality of life impairment; however, few studies have used specific tool for quality of life assessment this pathology, none being validated in French version. The aim of this study is to validate the parathyroid assessment of symptoms (PAS) questionnaire in French language to evaluate quality of life impairment and the impact of surgery in patients with primary hyperparathyroidism.
CONDITIONS
Official Title
Parathyroid Assessment of Symptoms French Version
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients with primary hyperparathyroidism (PHPT) defined by calcium > 2.60 mmol/L with elevated PTH or normal calcium with elevated PTH before surgery
- Patients consulting for PHPT surgery or at 6, 12, or 36 months after surgery
- Adult control patients consulting for thyroid surgery for benign nodules with normal thyroid function and no hypercalcemia, or post-operative consultation after cholecystectomy or appendectomy without complications
- Patients not opposed to participating in the study (returning questionnaires implies consent)
You will not qualify if you...
- Pregnant women at the time of completing questionnaires
- Minors or patients under guardianship or curatorship
- Patients with secondary or tertiary hyperparathyroidism defined by low calcium with elevated PTH or hypercalcemia with elevated PTH and history of kidney transplant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Nantes University Hospital
Nantes, Loire-Atlantique, France, 44093
Actively Recruiting
Research Team
E
Eric MIRALLIE
CONTACT
S
Samuel FREY
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
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