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Monocentric Study on the Use of Teriparatide in Children With hypoparathyroïdism

Bi-daily Injection of Subcutaneous Teriparatide in Children With Hypoparathyroidism: Single-center Experience

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04126941
Acronym
FOR-HYPO
Enrollment
9
Registered
2019-10-15
Start date
2019-06-01
Completion date
2020-12-31
Last updated
2019-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoparathyroidism

Keywords

Hypoparathyroidism, Teriparatide

Brief summary

Pediatric hypoparathyroidism is an orphan disease. Conventional management combines native and active vitamin D, calcium supplementation and sometimes phosphate binders, with the risk of long term hypercalciuria, nephrocalcinosis and further renal impairment. The use of teriparatide has been reported in adults (daily or bi-daily subcutaneous infusions) and in children (rather continuous subcutaneous infusion) as second-line therapy. The objective of this study is to obtain efficacy and safety data on the use of teriparatide in children with hypoparathyroidism to improve our knowledge of their management.

Interventions

OTHERSerum calcium concentrations results

To compare serum calcium concentrations results in patients with hypoparathyroidism before and three months after initiation of teriparatide therapy

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Patients with hypoparathyroidism * Patients treated with teriparatide * Patients followed in the reference center for calcium and phosphate metabolism diseases of Lyon. * For children under 18: patient and parent (s) / parent having been informed of the study and having expressed their non-opposition

Exclusion criteria

* No social security support

Design outcomes

Primary

MeasureTime frame
Serum calcium concentration3 months after treatment initiation

Secondary

MeasureTime frame
Serum calcium concentration1 month after treatment initiation

Countries

France

Contacts

Primary ContactJustine BACCHETTA, MD
justine.bacchetta@chu-lyon.fr4 27 85 61 30
Backup ContactSacha FLAMMIER, PHD
sacha.flammier@chu-lyon.fr4 27 85 66 69

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026