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Object Assessment of Improvement in Non-Specific Symptoms After Parathyroidectomy for Primary Hyperparathyroidism

Object Assessment of Improvement in Non-Specific Symptoms After Parathyroidectomy for Primary Hyperparathyroidism

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06337825
Enrollment
45
Registered
2024-03-29
Start date
2022-07-19
Completion date
2024-06-29
Last updated
2024-08-06

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

Conditions

Multinodular Goiter, Primary Hyperparathyroidism

Brief summary

Wearable electronic devices are becoming more prevalent in daily life, as they offer real time information on physiological parameters such as heart rate, activity level, oxygenation, and sleep patterns for their users. These wearable electronic devices are easy to install and offer no major risk or discomfort to the user. Implementation of these technologies into medicine has exponentially grown in the past decade with supporting evidence for their use in cardiovascular disease and sleep medicine. The investigators believe that these devices will be able to capture the changes associated with improvement in non-specific symptoms that have not been previously demonstrated.

Detailed description

Primary hyperparathyroidism (PHPT) may be more common than previously assumed.1 Historically, osteoporosis and nephrolithiasis were the only two indications for parathyroidectomy (PTX) based on symptomology.2 All other patients, even in the presence of non-specific symptoms related to PHPT, were not routinely recommended for surgery. Nowadays, however, there is increased understanding that a patient's quality of life (QOL) may be adversely affected by these non-specific symptoms.3 The American Association of Endocrine Surgeons (AAES) strongly recommends PTX in patients with these non-specific symptoms if they can be attributed to PHPT.4 Despite this, these neuropsychiatric, musculoskeletal, and gastrointestinal symptoms are overall difficult to quantify and the improvements in symptoms are mostly measured with QOL surveys. Even QOL surveys are subjective, and therefore, this may be a major barrier in broadening the indications for parathyroidectomy in patients with PHPT. To this day, there is no proposed objective metrics to quantify these improvements after parathyroidectomy. Furthermore, the effect of PHPT on cardiovascular risk has been studied, but so far the results are conflicting. The mechanisms for this increased cardiovascular risk are not fully understood. Nonetheless, this population demonstrates higher rates of hypertension, dyslipidemia, obesity, diabetes, and atherosclerosis compared to the general population. On the other hand, depression and sleep disturbances are also known factors for these comorbidities. It is possible that the neuropsychiatric symptoms of PHPT may contribute to a sedentary lifestyle and thus increase the cardiovascular risk. The association between these two have not been studied.

Interventions

BEHAVIORALActivity Tracker (Fitbit)

Wearable, activity tracker

DIAGNOSTIC_TESTHbA1C

Average blood glucose (sugar) levels reported as a percentage

BEHAVIORALThe PROMPT Questionnaire

The PROMPT Questionnaire which is a 30-question previously validated assessment for non-specific symptoms in PHPT, will be administered to patients preoperatively and at 2-weeks and 6-months postoperatively

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Study group: Consecutive patients older than 18 years old who will undergo PTX for PHPT. The indications and need for surgery will be independent from the research team. * Control group: Consecutive patients older than 18 years old who will undergo thyroidectomy for multinodular goiter (MNG). The indications and need for surgery will be independent from the research team.

Exclusion criteria

* Patients with recurrent or persistent PHPT will not be included. * Patients who are included but have evidence of recurrent or persistent PHPT based on six-month laboratory workup will be excluded from the final analysis (\<5% expected)4. * Established diagnosis of thyroid cancer or Graves' disease. * Musculoskeletal or neurologic disorders that affect the patient's activity level. * Cardiac arrhythmias that would interfere with the wearable electronic device measurement. * Sleep apnea and other sleep disturbances undergoing concurrent treatment.

Design outcomes

Primary

MeasureTime frameDescription
Change in resting heart rate over time among study participants as monitored by fitness tracker7 monthsTo assess the change in resting heart rate before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in number of awakenings during sleep over time among study participants as monitored by fitness tracker7 monthsTo assess the change in number of awakenings during sleep before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in % Deep Sleep over Total Sleep Minutes over time among study participants as monitored by fitness tracker7 monthsTo assess the change in % Deep Sleep over Total Sleep Minutes before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in steps over time among study participants as monitored by fitness tracker7 monthsTo assess the change in steps before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in total active minutes over time among study participants as monitored by fitness tracker7 monthsTo assess the change in total active minutes before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in% Active Calorie over Total Calories over time among study participants as monitored by fitness tracker7 monthsTo assess the change in % Active Calorie over Total Calories before and after parathyroidectomy in patients with Primary hyperparathyroidism
Change in glucose levels (HbA1C)7 monthsTo assess the change glucose control before and after parathyroidectomy in patients with Primary hyperparathyroidism.
Correlation of Quality of Life surveys with the PROMPT survey7 monthsTo correlate the measurements of patient health parameters with quality of life surveys before and after parathyroidectomy. This survey is comprised of 30 questions each with a 1 - 5 rating scale where lower scores indicate less pain, fatigue, soreness and higher scores indicate more fatigue, pain, soreness etc.

Countries

United States

Outcome results

None listed

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