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Clinical Trials/NCT04059380
NCT04059380
Completed
Not Applicable

Evaluation of iMmune Function in Post-surgical and AuToimmune HYpoparathyroidism: The EMPATHY Study

University of Roma La Sapienza1 site in 1 country40 target enrollmentMay 13, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypoparathyroidism
Sponsor
University of Roma La Sapienza
Enrollment
40
Locations
1
Primary Endpoint
Peripheral Blood Mononuclear Cells
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is an observational pilot study for the evaluation of immune function, infectious diseases, psychometric status and quality of life in patients with hypoparathyroidism compared to healthy controls.

Detailed Description

This is an observational pilot study for the evaluation of immune function, infectious diseases, psychometric status and quality of life in patients with hypoparathyroidism compared to healthy controls. All patients with Hypoparathyroidism will be on established conventional therapy with calcium supplements and calcitriol. According to guidelines, possible confounding factors (i.e. Vitamin D, serum magnesium levels) will be evaluated at screening visit. Age-, sex- and BMI- matched healthy controls will be enrolled. Patients and controls will undergo a screening visit (V0) and a baseline visit (V1) in the following month. The primary outcome will be the immune profiling of patients with hypoparathyroidism compared to healthy controls by the quantification of peripheral blood mononuclear cells (PBMC) subpopulations assessed by flow cytometry. Secondary Outcome Measures will be: Functional evaluation of PBMC cytokine secretion assessed by flow cytometry Evaluation of calcium signaling components expression compared to healthy controls Evaluation of PTHR1 expression in immune cells compared to healthy controls Evaluation of inflammatory cytokines production compared to healthy controls. Evaluation of quality of life compared to healthy controls. Quality of life will be measured by Short Form (SF)-36-Item Health Survey total score, SF-36-Item Health Survey physical component summary score and SF-36-Item Health Survey mental component summary score. Evaluation of infectious diseases frequencies and severity compared to healthy controls. Infectious diseases will be evaluated by an adaptation of Infectious Diseases Questionnaire (GNC). Psychometric evaluation by self-administered questionnaires: Beck depression Index, Middlesex Hospital Questionnaire. Sleep disturbances evaluation by The Pittsburgh Sleep Quality Index (PSQI) self reported questionnaire.

Registry
clinicaltrials.gov
Start Date
May 13, 2019
End Date
October 31, 2020
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Roma La Sapienza
Responsible Party
Principal Investigator
Principal Investigator

Andrea M. Isidori

Full Professor

University of Roma La Sapienza

Eligibility Criteria

Inclusion Criteria

  • Previously diagnosed (at least 6 months before enrolment) hypoparathyroidism which required daily calcium (≥1000mg/die) and calcitriol therapy;
  • Signed informed consent to participate in the study.

Exclusion Criteria

  • Transient hypoparathyroidism;
  • History of neoplasms, radiotherapy or chemotherapy in the last 5 years;
  • Clinical or laboratory signs of significant respiratory, hepatobiliary, or pancreatic disease;
  • Severe infections, surgery, trauma requiring hospitalization within 3 months before enrolment;
  • Severe chronic kidney disease (stage 4-5);
  • Any active blood or rheumatic disorders in the last 5 years

Outcomes

Primary Outcomes

Peripheral Blood Mononuclear Cells

Time Frame: baseline

Number of cells (number per mm3) of peripheral blood mononuclear cell subpopulations

Secondary Outcomes

  • Sleep disturbances(baseline)
  • Cell-specific Inflammatory Cytokine expression(baseline)
  • PTHR1 expression(baseline)
  • Infectious diseases frequency and severity(baseline)
  • Calcium Signaling evaluation(baseline)
  • Inflammatory cytokines levels(baseline)
  • Quality of life: SF-36-Item Health Survey questionnaire(baseline)
  • Psychometric evaluation(baseline)

Study Sites (1)

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