Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
150 participants
OBSERVATIONAL
2018-11-01
2020-11-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Post-thyroidectomy Dysphagia: An International Multicentric CONSORT - Compatible RCT
NCT04410601
Comparison of Quality of Life Between Patients Underwent Transoral Endoscopic Thyroid Surgery and Conventional Surgery
NCT03048539
Comparison of QoL for Sutureless Thyroidectomy
NCT02683551
Comparative Study Between Transcutaneous Ultrasonography and Direct Laryngoscopy for Assessment of Vocal Cord Mobility at the End of Thyroidectomy Operation
NCT06951295
Quality of Life in Patients Undergoing Parathyroidectomy
NCT00905866
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CROSSOVER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
parathyroidectomy cases
patients who will be operated for primary hyperparathyroidism
parathyroidectomy
routine parathyroidectomy will be done for the treatment of adenoma
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
parathyroidectomy
routine parathyroidectomy will be done for the treatment of adenoma
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* must be able to swallow tablets Planned operation for primary hyperparathyroidism
Exclusion Criteria
* insulin dependent diabetes
* thyroid disease
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Uşak University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Barış Sevinç
Assistant professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Barış Sevinç
Role: PRINCIPAL_INVESTIGATOR
Uşak University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Uşak University
Uşak, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
pthswalqol
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.