Viewing Study NCT00858104



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Study NCT ID: NCT00858104
Status: COMPLETED
Last Update Posted: 2014-05-26
First Post: 2009-03-06

Brief Title: Percutaneous Laser Ablation in Benign Thyroid NodulesLong Term Results
Sponsor: Elesta SRL
Organization: Elesta SRL

Study Overview

Official Title: Multicentric Randomized Controlled Study of Percutaneous Laser Ablation Versus Follow Up in Benign Thyroid Nodules Long Term Results
Status: COMPLETED
Status Verified Date: 2014-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Thyroid nodule pathologies occur frequently and represent a clinical issue for the endocrinologists surgeons nuclear physicians as well as the general practitioners The incidence of this pathology has been further highlighted by the introduction of the ultrasound examination into the clinical practice as 20 with impalpable thyroid nodules is now detected through ultrasound The majority of nodules are benign and characterized by slow growth and therefore treated with suppressive doses of levothyroxine Long-term levothyroxine treatment has however several well-known side effects and limitations

During the last years number of controlled studies have demonstrated that ultrasound guided percutaneous laser treatment PLA is able to reach the target lesion within the thyroid with a high level of precision and to destroy the thyroid tissue in a predictable and repeatable fashion without side effects

Aim of the study

1 to assess 1-year and 3-year effect of laser ablation therapy on the volume of benign thyroid nodules and on nodule-related symptoms and to compare these effects with findings in control group without active therapy
2 to assess the eventual re-occurence of thyroid lesions observed after other types of ablation treatment like percutaneous ethanol injection during a 3-year follow-up
3 to demonstrate reproducibility of results within different environments and under different operators
4 to validate eventual presence of major or minor side effects

To this aim we shall randomized 200 patients either for PLA 100 pts or standard follow-up Patients will be recruited treated and followed in 4 italian centers Ospedale Regina Apostolorum - Roma Arcispedale S Maria Nuova - Reggio Emilia Ospedale S Maria della Misericordia - Perugia Ospedale di Cisanello - Pisa by physicians with experience in PLAThe scientific coordinator of this multicentre study is dr Claudio Maurizio Pacella
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None