Observation of Histological Changes in Parathyroid Adenomas Following High Intensity Focused Ultrasound (HIFU) Treatment Procedure
Primary Purpose
Primary Parathyroid Adenomas
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Ultrasonic ablation device
Sponsored by
About this trial
This is an interventional basic science trial for Primary Parathyroid Adenomas focused on measuring Primary hyperparathyroidism, High Intensity Focused Ultrasound, Parathyroid tumor, Parathyroid hormone, Calcium
Eligibility Criteria
Inclusion Criteria:
- Male or female patient 18 years or older.
- Patients with diagnosed primary hyperparathyroidism (clinical symptoms and/or biochemical disturbances) scheduled for parathyroidectomy.
- One diseased parathyroid gland, visualized by ultrasonography.
- The diseased targeted parathyroid gland accessible for HIFU treatment (anonymised ultrasonographic images to be sent to the sponsor's technical team for validation).
- Normal pretreatment nasofibroscopy.
- Voluntary signed informed consent.
Exclusion Criteria:
Inaccessibility or high risk of targeting neighbouring structures, as evidenced by:
- Targeted area located less than 2 mm laterally from the oesophagus or the carotid artery
- Targeted area located less than 3 mm laterally from the trachea,
- Significant hyperechoic area with a posterior shadow located less than 10 mm behind the targeted area (behind to be understood as posterior to the targeted area in the direction of the HIFU beam)
- Investigator appreciation of any abnormal blood test that could contraindicate treatment with HIFU (bleeding abnormalities)
- Known spondylitis of the neck vertebrae
- Head and/or neck disease that prevents hyperextension of neck.
- Known history of parathyroid or other neoplasias in the neck region.
- History of neck irradiation
- Patients whose concurrent illnesses, disability, or geographical residence would hamper attendance at required study visit
- Pregnant or lactating woman.
- Female patient of childbearing age if not having a suitable contraception method.
- Patients who have received any investigational drug or device within the last 15 days and/or patients who are currently participating in another clinical trial.
Sites / Locations
- Hôpital Privé des Peupliers
- Cochin Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
HIFU treatment
Arm Description
Outcomes
Primary Outcome Measures
Histology of excised gland.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01060982
Brief Title
Observation of Histological Changes in Parathyroid Adenomas Following High Intensity Focused Ultrasound (HIFU) Treatment Procedure
Official Title
Observation of Histological Changes in Parathyroid Adenomas Following High Intensity Focused Ultrasound (HIFU)Treatment Procedure: A Monocentre, Open, Uncontrolled Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
January 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Theraclion
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is a multicentre, open, uncontrolled trial for the observation of histological changes in parathyroid adenomas following high intensity focused ultrasound (HIFU).
This study will be conducted in France in 10 patients with primary hyperparathyroidism scheduled for a parathyroidectomy. The patient will receive an HIFU treatment in the center of the adenoma before the surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Parathyroid Adenomas
Keywords
Primary hyperparathyroidism, High Intensity Focused Ultrasound, Parathyroid tumor, Parathyroid hormone, Calcium
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
HIFU treatment
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Ultrasonic ablation device
Other Intervention Name(s)
TH-One
Intervention Description
One High Intensity focused ultrasound session before surgery. Use of appropriate energy for each patient
Primary Outcome Measure Information:
Title
Histology of excised gland.
Time Frame
After surgery performed the same day as High intensity focused ultrasound treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female patient 18 years or older.
Patients with diagnosed primary hyperparathyroidism (clinical symptoms and/or biochemical disturbances) scheduled for parathyroidectomy.
One diseased parathyroid gland, visualized by ultrasonography.
The diseased targeted parathyroid gland accessible for HIFU treatment (anonymised ultrasonographic images to be sent to the sponsor's technical team for validation).
Normal pretreatment nasofibroscopy.
Voluntary signed informed consent.
Exclusion Criteria:
Inaccessibility or high risk of targeting neighbouring structures, as evidenced by:
Targeted area located less than 2 mm laterally from the oesophagus or the carotid artery
Targeted area located less than 3 mm laterally from the trachea,
Significant hyperechoic area with a posterior shadow located less than 10 mm behind the targeted area (behind to be understood as posterior to the targeted area in the direction of the HIFU beam)
Investigator appreciation of any abnormal blood test that could contraindicate treatment with HIFU (bleeding abnormalities)
Known spondylitis of the neck vertebrae
Head and/or neck disease that prevents hyperextension of neck.
Known history of parathyroid or other neoplasias in the neck region.
History of neck irradiation
Patients whose concurrent illnesses, disability, or geographical residence would hamper attendance at required study visit
Pregnant or lactating woman.
Female patient of childbearing age if not having a suitable contraception method.
Patients who have received any investigational drug or device within the last 15 days and/or patients who are currently participating in another clinical trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe BONNICHON, MD
Organizational Affiliation
Cochin Hospital, Paris, Fance
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Privé des Peupliers
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Cochin Hospital
City
Paris
ZIP/Postal Code
75014
Country
France
12. IPD Sharing Statement
Learn more about this trial
Observation of Histological Changes in Parathyroid Adenomas Following High Intensity Focused Ultrasound (HIFU) Treatment Procedure
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