No registrations found.
ID
Source
Brief title
Health condition
Parathyroid disease
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary objective of this study are:
- To assess the physical quality of life in patients with hypoparathyroidism as measured by the SF-36 questionnaire.
- To determine the Thyroid-Related quality of life in patients with hypoparathyrodism
- To determine the cognitive and functional outcomes in patients with hypoparathyrodism
- To determine the burden of disease in patients with hypoparathyroidism
Secondary outcome
The secondary objective of this study is to the determine the burden of disease in patients with hypoparathyroidism, attributed to hypoparathyroidism and hypoparathyroidism treatment by measuring medication use, the absence of work/return to work, extra hospital visits, comorbidities, hypoparathyroidism related laboratory parameters.
Background summary
Rationale: Hypoparathyroidism is caused by absent or insufficient amounts of parathyroid hormone. This is a relatively rare disease, but unfortunately a common complication after thyroid surgery due to inadvertent damage to the parathyroid glands. Although the relatively easy treatment with calcium supplementation suggests that the burden of disease is low, Hadker et al. assessed 374 adults with hypoparathyroidism (of which 80% was due to surgical interference) and found that despite medical treatment, patients did not function well in their day-to-day life. Currently, epidemiological studies are sparse and quality of life studies are slowly advancing. The possible future treatment of these patients with synthetic PTH renders is important to assess the burden of disease and quality of life in a matched control study.
Objective: The objective is to assess the impact of hypoparathyroidism on quality of life and the burden of disease.
Study design: A prospective observational case-control study will be performed.
Study population: All adult patients with persisting hypoparathyroidism and a matched cohort without hypoparathyroidism, who underwent a total or completion thyroidectomy are eligible for inclusion.
Intervention: Not applicable
Main study parameters/endpoints: Main study endpoints are quality of life in patients with hypoparathyroidism as measured by the physical component score of the SF-36, thyroid related quality of life (ThyPro), functional and cognitive assessment (CIS and PROMIS) and burden of disease as measured by EQ-5D-5L. Other endpoints are extra hospital visits, employment status, comorbidities and hypoparathyroidism related laboratory parameters.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients will be asked to visit the outpatient department one time at the beginning of inclusion. If possible, this visit will be combined with a regular care visit. During this visit a venipuncture will be performed and in total 5 tubes of blood will be drawn. Risks associated with venipunctures are hematoma and pain. Patients will also be asked to fill in five questionnaires at three time points. Furthermore, patients will receive a phone call every three months to answer questions regarding their employment status, medication, comorbidities and extra hospital visits. There is no direct benefit for the patients.
Study objective
It is expected that patients with hypoparathyroidism have a lower quality of life.
Study design
The duration of patient participation will be up to 1 year. Patients will be asked to visit the Erasmus Medical Center at baseline and to fill in questionnaires at three time points (baseline, 6 months, 12 months).
Inclusion criteria
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Patients who are aged 18 years or older at the time of inclusion
- Patients who gave informed consent
- Both cases and controls underwent (completion) thyroidectomy
- Cases have persisting hypoparathyroidism according to the previously mentioned definition and controls do not
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Patients who are not able to provide written informed consent
- No adequate understanding of the Dutch language
- Parathyroid disease or parathyroid surgery
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL7490 |
Other | METC Erasmus Medical Centre : MEC-2018-1615 |