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NCT06337825 · ClinicalTrials.gov registry record

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

A clinical trial of Primary Hyperparathyroidism and Multinodular Goiter, sponsored by The Cleveland Clinic.

Completed
Registry status
45
Enrollment target
1
Study location

NCT06337825 is a study of Primary Hyperparathyroidism and Multinodular Goiter that has completed, run by The Cleveland Clinic. The registered enrollment target is 45 participants, below the 745-participant average among 7 other Primary Hyperparathyroidism trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06337825, a study of Primary Hyperparathyroidism and Multinodular Goiter, has completed, sponsored by The Cleveland Clinic.

COMPLETED
Registry status
45 participants
Enrollment target
1
Study location

Study 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.

Interventions

  • BEHAVIORAL Activity Tracker (Fitbit)
  • DIAGNOSTIC_TEST HbA1C
  • BEHAVIORAL The PROMPT Questionnaire

Study Locations (1)

Ohio

  • The Cleveland Clinic Foundation - Cleveland

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2022-07-19
Est. Completion 2024-06-29

Sponsor

The Cleveland Clinic

688 total trials

What the Registry Record Tells You About NCT06337825

The ClinicalTrials.gov registry entry for NCT06337825 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 745-participant average among 7 other Primary Hyperparathyroidism trials with a reported enrollment target (94% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Primary Hyperparathyroidism appearing as the primary indexed condition, and to 3 interventions - of which Activity Tracker (Fitbit) is the first listed.

NCT06337825 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT06337825 about?

NCT06337825 is a clinical study titled "Object Assessment of Improvement in Non-Specific Symptoms After Parathyroidectomy for Primary Hyperparathyroidism". 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...

What is the current status of trial NCT06337825?

This trial is currently completed. The enrollment target is 45 participants. The study started on 2022-07-19. Estimated completion is 2024-06-29.

What conditions does trial NCT06337825 study?

This clinical trial studies the following conditions: Primary Hyperparathyroidism, Multinodular Goiter.

What interventions are being tested in trial NCT06337825?

The interventions under investigation include: Activity Tracker (Fitbit) (BEHAVIORAL), HbA1C (DIAGNOSTIC_TEST), The PROMPT Questionnaire (BEHAVIORAL).

Who is sponsoring clinical trial NCT06337825?

This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06337825 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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