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NCT05501041 Clinical Trial

Measuring Symptom Relief After Radiofrequency Ablation of the Thyroid

Thyroid Clinical Trial

Official title:
Quantification of Symptom Relief Following Percutaneous Ablation of the Thyroid

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT05501041
Other study ID # 22-007581
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date August 22, 2022
Est. completion date August 2025

Study information
Verified date September 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to measure the impact of thyroid radiofrequency ablation procedure on patients with thyroid-related symptoms using a modified pre-existing scoring system.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 300
Est. completion date August 2025
Est. primary completion date August 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Undergoing Radiofrequency Ablation (RFA) for symptomatic thyroid nodule(s). Exclusion Criteria: - Decline to participate in research.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Mayo Clinic Rochester Rochester Minnesota

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in symptoms before and after ablation Measured using a modified 6-item SYS questionnaire that objectively measures patient symptoms on a scale of 0=none, 1=moderate, 2=severe Baseline and 1-, 3-, 6-, 12-, 18-, and 24-months following treatment
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