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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03968510
Other study ID # pthswalqol
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2018
Est. completion date November 1, 2020

Study information

Verified date June 2021
Source Usak University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Swallow related quality of life before and after parathyroidectomy will be evaluated in patients with primary hyperparathyridism.


Description:

Patients who will undergone parathyroidectomy for primary hyperparathyroidism will be included in the study. Swal-Qol and Sf-36 forms will be used for evaluation of quality of life before and 1 month after the surgery. The change in the quality of life and swallowing related quality of life will be evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date November 1, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - no diagnosis of Alzheimers disease - must be able to swallow tablets Planned operation for primary hyperparathyroidism Exclusion Criteria: - secondary or tertiary hyperparathyroidism - insulin dependent diabetes - thyroid disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
parathyroidectomy
routine parathyroidectomy will be done for the treatment of adenoma

Locations

Country Name City State
Turkey Usak University Usak

Sponsors (1)

Lead Sponsor Collaborator
Usak University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in quality of life Quality of life will be evaluated using short form 36 6 months
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