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NCT04759053 Clinical Trial

Effectiveness of Core-Needle US Guided Biopsy as Primary Tool For Diagnosis of Thyroid Nodules

Thyroid Nodule Clinical Trial

Official title:
Effectiveness of Core-Needle US Guided Biopsy as Primary Tool For Diagnosis of Thyroid Nodules, A Prospective Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04759053
Other study ID # 124569124577
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date February 1, 2018

Study information
Verified date February 2021
Source Kafrelsheikh University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aimed to determine the best intervention between Core biopsy and Fine needle aspiration in diagnosis of thyroid malignancy.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date February 1, 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - patients with nodules larger than 1 cm in diameter and suspicious ultrasound criteria with TIRADS category III or higher. Exclusion Criteria: - Patients with a history of hemodynamic instability or inadequate coagulation profile were excluded

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• FNB
Fine needle aspiration from the nodules
• Core biopsy
Core biopsy from thyroid nodules

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Kafrelsheikh University Alexandria University

Outcome
Type Measure Description Time frame Safety issue
Primary Number of samples in FNB and CNB matching the final pathology Comparing number of samples in FNB and CNB that make same diagnosis as the final postoperative pathology 7 days
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