Tunisian Clinical Registry on Hypoparathyroidism and Pseudo-hypoparathyroidism
Launched by DACIMA CONSULTING · May 31, 2024
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The Tunisian Clinical Registry on Hypoparathyroidism and Pseudo-hypoparathyroidism is a study that aims to gather information about patients who have issues with their parathyroid hormone, which helps regulate calcium levels in the body. Specifically, it looks at two conditions: hypoparathyroidism, where the body does not produce enough of this hormone, and pseudo-hypoparathyroidism, where the body is unable to respond properly to it. This study will collect data on the health, laboratory results, and treatments of these patients in Tunisia.
To participate, individuals must have hypoparathyroidism, which is defined by low calcium levels in the blood along with low or normal parathyroid hormone levels. However, those who have had recent neck surgery, temporary forms of low parathyroid hormone activity, or other specific causes of low calcium levels, such as vitamin D deficiency or chronic kidney disease, will not be eligible. Since the study is observational, participants will be asked to provide information about their condition, but there will be no new treatments or interventions given. This study will help improve understanding of these conditions and potentially guide better care in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Hypoparathyroidism defined by low serum calcium \< 2.2 mmol/l (\< 88 mg/l) associated with inadequate PTH (low or normal) and normal creatinine
- Exclusion Criteria:
- • Cervical surgery \< 6 months.
- • Transient (neonatal, etc.) or functional (dysmagnesemia, etc.) hypoparathyroidism.
- • Other causes of hypocalcemia: vitamin D deficiency, chronic renal failure, etc.
- • Familial hypocalcemia hypercalciuria.
- • Pseudo-pseudo-hypoparathyroidism.
About Dacima Consulting
Dacima Consulting is a leading clinical trial sponsor specializing in innovative solutions for the pharmaceutical and biotechnology industries. With a commitment to advancing healthcare, Dacima leverages cutting-edge technology and a team of experienced professionals to design, manage, and execute clinical trials efficiently and effectively. Their comprehensive services encompass protocol development, regulatory support, data management, and statistical analysis, ensuring high-quality results that facilitate the drug development process. Dacima Consulting is dedicated to enhancing patient outcomes through rigorous research, strategic collaboration, and a patient-centered approach.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Sfax, , Tunisia
Patients applied
Trial Officials
Nabila Rekik Mejdoub, MD
Study Chair
Société Tunisienne D'endocrinologie De Diabétologie Et Des Maladies Métaboliques
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported