Percutaneous Ethanol Injection for Primary Papillary Thyroid Microcarcinoma

Papillary Thyroid Cancer Clinical Trial

Official title:

Percutaneous Ethanol Injection for Primary Papillary Thyroid Microcarcinoma

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01974284
• Other study ID #: HIC1312013168
• Status: Terminated
• Phase: N/A
• Start date: March 2014
• Est. completion date: June 29, 2017

Study information

• Verified date: November 2019
• Source: Yale University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

We assess the effectiveness of percutaneous ethanol ablation for the treatment of thyroid cancer.

Description:

We hypothesize that percutaneous ethanol ablation (PEA) for primary papillary thyroid microcarcinoma (PTMC) has equivalent oncologic outcomes to current treatment options including observation, thyroid lobectomy and total thyroidectomy. In addition, we hypothesize that it will yield superior long-term quality of life, including measures of pain, voice, and cosmesis than standard surgical therapy (total thyroidectomy). If our hypotheses are correct, the findings of this study have the potential to fundamentally change clinical management of this group of patients.

This study was changed from its initial design: a 2 arm study comparing PEA to surgery (Amended April 30, 2015). The change in design was made based on several discussions within Yale Endocrine Surgery, with patients diagnosed with PTMC, and knowledge of other institutions performing PEA for PTMC as standard of care.

The study team had been contacted by numerous potential subjects interested in PEA who were unwilling to be randomized to surgery. Because patients interested in PEA appeared to be firmly against the idea of thyroidectomy, we believed that we would be unable to enroll sufficient patients to this study as the protocol originally stood.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 7
• Est. completion date: June 29, 2017
• Est. primary completion date: March 2, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age 18 years and older

• Diagnosis: single, cytology-proven papillary thyroid carcinoma measuring 1 cm or less in diameter (microcarcinoma, T1a), without visible extrathyroidal extension, and with negative central and lateral neck lymph nodes by ultrasound

Exclusion Criteria:

• Patient refusal to participate

• History of prior thyroid or parathyroid surgery

• Previous recurrent laryngeal nerve injury

• Inability to make decisions or comply with follow up

• Co-existing indication for thyroidectomy

• Aggressive cytological or molecular features

• Multifocal papillary thyroid carcinoma

• Pregnant or breast-feeding

• Anatomically unfavorable location of the tumor (proximity to recurrent laryngeal nerve or trachea)

• Documented or suspected distant metastasis

• History of radiation to neck or face

• Family history of thyroid cancer

Related Conditions & MeSH terms

• Papillary Thyroid Cancer
• Thyroid Cancer, Papillary
• Thyroid Diseases
• Thyroid Neoplasms

Intervention

Drug:
• percutaneous ethanol ablation
The volume of 99% ethanol to be injected is calculated using a standardized formula. Ethanol is instilled with a needle under ultrasound guidance after administration of local anesthesia.

Locations

Country	Name	City	State
United States	Endocrine Surgery Smilow Cancer Hospital at Yale-New Haven	New Haven	Connecticut

Sponsors (1)

Lead Sponsor	Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Disease-free	Primary endpoint of the study consists of the oncological outcome, which includes the disease-free status of the patients.	5 years
Primary	Overall Survival	Primary endpoint of the study consists of the oncological outcome, which includes the overall survival of the patients.	5 years
Secondary	Quality of Life	The Short-Form-36 (SF-36) health survey is a patient-reported survery that evaluates the patient's health status. It consists of 8 scaled scores which are the weighted sums of the questions in each section. The 8 sections that are tested are vitality, physical functioning, bodily pain, general role functioning, emotional role functioning, social role functioning, and mental health. Each scale is directly transformed into a 0-100 scale; the higher the score, the less disability (i.e. the score of 0 is equivalent to maximal disability, and the score of 100 is equivalent of no disability). The SF-36 is a set of easily-administered quality-of-life measures and is a validated tool to evaluate patient quality of life.	5 years
Secondary	Patient Satisfaction	Patient satisfaction will be assessed by evaluating the following: pain with the "Brief Pain Inventory" (BPI), voice with the "Voice Handicap Index" (VHI) and cosmesis with the "Patient and Observer Scar Assessment Scale" (POSAS). The BPI is a simple, well-accepted instrument for the objective assessment of pain. The VHI is an established tool used to assess voice after an intervention. POSAS is a validated tool for the evaluation of surgical scars.	5 years