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Cohort Primary Hyperparathyroidism

Prospective Cohort Primary Hyperparathyroidism

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05469087
Acronym
CoHPT
Enrollment
403
Registered
2022-07-21
Start date
2016-03-31
Completion date
2027-02-24
Last updated
2025-09-08

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

Conditions

Primary Hyperparathyroidism

Keywords

Primary hyperparathyroidism, Parathyroidectomy

Brief summary

CoHPT is a prospective, monocentric, observational cohort including all patients diagnosed with primary hyperparathyroidism in Nantes University Hospital, aiming to study the outcomes associated with parathyroidectomy. Clinical and biochemical evaluation is performed at the inclusion, and 6, 12, 36 and 60 months. A biocollection is collected. The main hypotheses are that parathyroidectomy could improve cardiovascular, renal, bone, and cardiovascular outcomes along with quality of life.

Detailed description

Primaty hyperparathyroidism is the third most frequent endocrine disorder, which only curative treatment is the parathyroidectomy (approximately 8000/year). However, evidences suggest that the mildest forms of PHPT could be safely monitored with simple surveillance. However, to define surgical indications is challenging because data regarding the impach of surgery on several outcomes (namely cardiovascular, bone, renal or quality of life) are controversial. CoHPT is a prospective, monocentric, observational cohort including all consecutive patients diagnosed with sporadic primary hyperparathyroidism in Nantes University Hospital aiming to study the outcomes associated with parathyroidectomy. Patients are followed even if surgery is not performed. A systematic clinical and biochemical evaluation is performed at the inclusion, and 6, 12, 36 and 60 months. These informations include demographic and general medical data, pre-operative imaging exams, post-operative outcomes, histopathological analysis, evaluation of the impact of primary hyperparathyroidism and its surgery on target organs (bone, kidney, cardiovascular) and quality of life. Fasting blood samples are also collected to constitute a biocollection, in order to measure biomarkers related to the bone remodeling and the cardiovascular risk. The objectives are: * To know the long-term consequences of the primary hyperparathyroidism treatment or observation. * To better define the surgical indications * To better understand the mechanisms of the cardiovascular impairment by using the biocollection * To study the medico-economics consequences of the surgical management versus simple surveillance

Interventions

None listed

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

• Age \> 18

Exclusion criteria

* Age \< 18 * Pregnancy / lactation * Adults underguardianship * Secondary/tertiary hyperparathyroidism * Multiple endocrine neoplasia

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of cardiovascular events, after parathyroidectomy for primary hyperparathyroidismBetween inclusion and 12 months after surgeryCardiovascular events include myocardial infarction, cerebrovascular and peripheral arterial events
Change in LDL-cholesterol concentration after surgeryBetween inclusion and 12 months after surgeryPlasma LDL-cholesterol (mg/dL) will be directly measured using enzymatic method
Change in HDL-cholesterol concentration after surgeryBetween inclusion and 12 months after surgeryPlasma HDL-cholesterol (mg/dL) will be measured using enzymatic method
Change in plasma triglycerides concentration after surgeryBetween inclusion and 12 months after surgeryPlasma triglycerides (mg/dL) will be measured using enzymatic method
Change in homeostasis model assessment HOMA-IR index after surgeryBetween inclusion and 12 months after surgeryHOMA-IR is calculated using fasting plasma glucose and insulin level, with the following formula: (fasting plasma insulin (mIU/L) × fasting plasma glucose (mmol/L))/22.5
Change in homeostasis model assessment HOMA-B index after surgeryBetween inclusion and 12 months after surgeryHOMA-B is calculated using fasting plasma glucose and insulin level, with the following formula: 20 × fasting plasma insulin (mIU/L)/\[fasting plasma glucose (mmol/L) - 3.5\]
Change in arterial stiffness after surgeryBetween inclusion and 12 months after surgeryArterial stiffness is reflected by the measurement of the pulse wave velocity using the PoPmeter® instrument

Secondary

MeasureTime frameDescription
Change in bone mineral density after parathyroidectomyBetween inclusion and 12 months after surgeryBone mineral density is measured using Dual X-ray absorptiometry on lumbar spine, left hip, left femoral neck and left distal radius
Change in bone-specific alkaline phosphatasesBetween inclusion and 12 months after surgeryAlkaline phosphatases (IU/L) are measured using ELISA enzymatic method
Change in P1NPBetween inclusion and 12 months after surgeryP1NP (µg/L) are measured using ELISA enzymatic method
Change in plasma CTXBetween inclusion and 12 months after surgeryCTX (µg/L) are measured using ELISA enzymatic method
Occurrence of cardiovascular events, after parathyroidectomy for primary hyperparathyroidismBetween inclusion and 60 months after surgeryCardiovascular events include myocardial infarction, cerebrovascular and peripheral arterial events
Change in the mental component score of the SF-36 questionnaire after surgeryBetween inclusion and 36 months after surgeryThe mental component score is calculated from 4 items of the SF-36 questionnaire related to mental health. Results are expressed as a ratio between the included patients with values expected in an age- and sex-matched French reference population.
Change in renal outcomes (estimated glomerular filtration rate) after parathyroidectomyBetween inclusion and 60 months after surgeryEstimated glomerular filtration rate will be calculated using the CKD-EPI equation from the measured serum creatinine
Medico-economic impact of parathyroidectomy for primary hyperparathyroidism in comparison with simple surveillance60 months after surgeryTakes into account the incidence of the worsening of cardiac and bone comorbidities and surgical complications. Data will be cross-referenced by probabilistic matching with the data of the Système National d'Information Interrégimes d'Assurance Maladie (SNIIR-AM)
Change in the physical component score of the SF-36 questionnaire after surgeryBetween inclusion and 36 months after surgeryThe physical component score is calculated from 4 items of the SF-36 questionnaire related to physical health. Results are expressed as a ratio between the included patients with values expected in an age- and sex-matched French reference population (available in Perneger T, Leplège A, Ecosse E. Le questionnaire MOS SF-36: manuel de l'utilisateur et guide d'interprétation des scores; Paris: Editions Estem. 2001:1-156.)
Change in LDL-cholesterol concentration after surgeryBetween inclusion and 60 months after surgeryPlasma LDL-cholesterol (mg/dL) will be directly measured using enzymatic method
Change in HDL-cholesterol concentration after surgeryBetween inclusion and 60 months after surgeryPlasma HDL-cholesterol (mg/dL) will be measured using enzymatic method
Change in plasma triglycerides concentration after surgeryBetween inclusion and 60 months after surgeryPlasma triglycerides (mg/dL) will be measured using enzymatic method
Change in homeostasis model assessment HOMA-IR index after surgeryBetween inclusion and 60 months after surgeryHOMA-IR is calculated using fasting plasma glucose and insulin level, with the following formula: (fasting plasma insulin (mIU/L) × fasting plasma glucose (mmol/L))/22.5
Change in homeostasis model assessment HOMA-B index after surgeryBetween inclusion and 60 months after surgeryHOMA-B is calculated using fasting plasma glucose and insulin level, with the following formula: 20 × fasting plasma insulin (mIU/L)/\[fasting plasma glucose (mmol/L) - 3.5\]
Change in arterial stiffness after surgeryBetween inclusion and 60 months after surgeryArterial stiffness is reflected by the measurement of the pulse wave velocity using the PoPmeter® instrument

Countries

France

Contacts

Primary ContactEric MIRALLIE, PHD
eric.mirallie@chu-nantes.fr33 2 40 08 31 66

Outcome results

None listed

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