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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03106337
Other study ID # 2007P001161
Secondary ID
Status Completed
Phase N/A
First received April 25, 2014
Last updated April 3, 2017
Start date January 2010
Est. completion date March 2016

Study information

Verified date April 2017
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

As many as 70-85% subjects diagnosed with a follicular lesion on biopsy and undergoing surgery will have benign lesions verified by histopathology after surgery.

Currently there is no method of pre-operatively diagnosing benign follicular lesions, as a result these subjects will have had surgery for diagnosis of a benign lesion.

The aim of this study is to see whether shear-wave elastography, a new ultrasound technology can help pre-operatively diagnose benign follicular lesions. If successful, a lot of patients will not need surgery for the diagnosis of a benign lesion.

The main goal of this study will be to evaluate the diagnostic accuracy of a new ultrasound technology (shear-wave elastography - SWE) for the diagnosis of malignancy in follicular lesions. Participants who have been diagnosed with a follicular lesion on thyroid biopsy and are scheduled for thyroid surgery will be eligible to participate. All participants will undergo a detailed ultrasound examination prior to their surgery. The results of the ultrasound will be compared with histopathology after surgery to test the diagnostic accuracy of SWE.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date March 2016
Est. primary completion date May 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients diagnosed with a Follicular Neoplasm on fine needle aspiration biopsy

- Patients >18 years of age

Exclusion Criteria

Study Design


Intervention

Device:
Shear Wave Sonoelastography
Shear Wave Sonoelastography is performed on patients scheduled for partial/total thyroidectomy. Results are compared with pathology from surgical excision.

Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shear Wave Elastography Values in kiloPascals (kPa) Elastography provides a quantitative score of thyroid nodule stiffness that is expected to correlate with the biological nature of the nodule.
We will compare mean elastography values of all benign lesions with mean values of all malignant lesions on histopathology obtained post surgery.
Baseline (Day 0).
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