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NIRF for Parathyroid Visualization: a Pilot Study

Primary Purpose

Thyroid Disease

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
NIRF imaging in thyroid surgery
Sponsored by
Maastricht University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Thyroid Disease focused on measuring Near infrared fluorescence, ICG, Parathyroid gland

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female patients, aged 18 years and above
  • Scheduled for elective total or hemi thyroidectomy
  • Normal liver and renal function
  • No known hypersensitivity for iodine or ICG
  • Able to understand the nature of the study procedures
  • Willing to participate and give written informed consent

Exclusion Criteria:

  • Age < 18 years
  • Liver or renal insufficiency
  • Known ICG, iodine, penicillin or sulfa hypersensitivity
  • Pregnancy or breastfeeding
  • Not able to understand the nature of the study procedure
  • i.v. heparin injection in the last 24h (LMWH not contraindicated)
  • Not willing to participate

Sites / Locations

  • Maastricht University Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

NIRF imaging in thyroid surgery

Arm Description

7.5 mg ICG is administered i.v. and the system will be switched to fluorescence mode. If needed, a second dose of 7.5 mg ICG can be administered. After identification of the parathyroid glands, surgery will continue until there is a desire to visualize the parathyroid glands again, another dose of ICG can be given. After complete removal of thyroid, another 7.5 mg of ICG will be given to assess the perfusion of the parathyroid gland. Directly after the procedure the researcher will ask the surgeon whether he/she thinks the technique is feasible. After surgery, the serum calcium levels will be determined in patients after total thyroidectomy on day 1, 2 and after two weeks. TSH will be determined after 2 weeks. The thyroid specimen will be send to pathology. In the specimen, the pathologist will search for parathyroid glands. Video recordings will be analyzed, quantifying the fluorescence signal compared to the background: measuring the TBR.

Outcomes

Primary Outcome Measures

Time to identification of parathyroid glans
Can the parathyroid glands be identified earlier with NIRF light? Time until identification in NIRF and white light will be compared.

Secondary Outcome Measures

Total surgical time
Histology: are parathyroid glands in the specimen? (as in standard care)
immediately after surgery, the thyroid specimen will be send to the pathology department for histological examination as in standard care, with extra attention on wether there are parathyroid glands in the specimen.
Subjective opinion surgeon about the usefulness of the technique
Intra-operative complications due to the use of the technique

Full Information

First Posted
January 3, 2017
Last Updated
March 13, 2018
Sponsor
Maastricht University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03012438
Brief Title
NIRF for Parathyroid Visualization: a Pilot Study
Official Title
The Use of Near-Infrared Fluorescence Imaging in Parathyroid Visualization During Thyroid Surgery: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
March 23, 2017 (Actual)
Primary Completion Date
February 1, 2018 (Actual)
Study Completion Date
March 12, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
During surgery in which the thyroid is removed (thyroidectomy), the identification of parathyroid glands, that should be saved, can be challenging. Therefore, there is need for accurate intraoperative guidance. Earlier animal studies show that the parathyroid glands can be identified by the use of the Near Infrared Fluorescent dye Indocyanine green (ICG). Our hypothesis is therefore, that the use of ICG-based fluorescence imaging during thyroid surgery will provide real-time intraoperative visualization of the parathyroid glands. This prospective observational feasibility study aims to evaluate the feasibility of the use of ICG in identifying the parathyroid glands during thyroid surgery. 30 patients (age >18 years) who are already regularly scheduled for thyroid surgery; i.e. patients undergoing total thyroidectomy are suitable for inclusion. In all patients, undergoing total thyroidectomy infrared fluorescence imaging, using a per-operative intravenous injection of 7.5 mg ICG, will be tested on feasibility and imaging characteristics.
Detailed Description
In this study, the feasibility of the use of NIR fluorescence imaging for the identification of the parathyroid glands during thyroid surgery will be explored. Per-operatively: The surgery will start as usual. When the surgeon would normally search for the parathyroid glands, 7.5 mg of ICG will be administered intravenously through the infusion in the patients arm. An intravenous administration is chosen because of the minimal invasive nature and results of the described earlier case series in which ICG was also administered via peripheral infusion. Directly after that, the fluorescence system can be switched to fluorescence mode. The surgeon will determine whether the parathyroid glands are visible now. If needed, due to washout, a second dose of 7.5 mg of ICG can be administered. After identification of the parathyroid glands, surgery will continue as in the standard situation, until there is a desire to visualize the parathyroid glands again, then another dose of ICG can be given. Time until first identification of the parathyroid glands and total surgical time will be measured. After complete removal of the thyroid, another 7.5 mg of ICG will be administered intravenously to visualize the vascularization of the parathyroid gland. The intensity will be subjectively scored: 1 parathyroid black after injection of ICG, 2 partially vascularized, or 3 parathyroid is green; well vascularized. The fluorescence system will be used to record the whole procedure. Directly after the procedure the researcher will ask the surgeon whether he or she thinks the technique is feasible. Postoperatively: As in standard care, after thyroid surgery, the serum calcium levels will be determined. Low calcium levels can indicate misidentification of parathyroid glands. These calcium levels are determined only in patients after total thyroidectomy on day 1, 2 and after two weeks. Also TSH will be determined after two weeks as in standard care. The thyroid specimen will be send to pathology. In the specimen, the pathologist will search for parathyroid glands, as is standard care. Furthermore, video recordings will be analyzed, quantifying the fluorescence signal compared to the background: measuring the Target to Background Ratio. Also, in these video recordings the time until visualization of the parathyroid glands will be reassessed by an independent expert.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid Disease
Keywords
Near infrared fluorescence, ICG, Parathyroid gland

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NIRF imaging in thyroid surgery
Arm Type
Experimental
Arm Description
7.5 mg ICG is administered i.v. and the system will be switched to fluorescence mode. If needed, a second dose of 7.5 mg ICG can be administered. After identification of the parathyroid glands, surgery will continue until there is a desire to visualize the parathyroid glands again, another dose of ICG can be given. After complete removal of thyroid, another 7.5 mg of ICG will be given to assess the perfusion of the parathyroid gland. Directly after the procedure the researcher will ask the surgeon whether he/she thinks the technique is feasible. After surgery, the serum calcium levels will be determined in patients after total thyroidectomy on day 1, 2 and after two weeks. TSH will be determined after 2 weeks. The thyroid specimen will be send to pathology. In the specimen, the pathologist will search for parathyroid glands. Video recordings will be analyzed, quantifying the fluorescence signal compared to the background: measuring the TBR.
Intervention Type
Device
Intervention Name(s)
NIRF imaging in thyroid surgery
Other Intervention Name(s)
Near Infrared Fluorescence Imaging, Indocyanine green
Intervention Description
a fluorescence imaging system and 7.5 mg of ICG will be used to visualize the parathyroids glands.
Primary Outcome Measure Information:
Title
Time to identification of parathyroid glans
Description
Can the parathyroid glands be identified earlier with NIRF light? Time until identification in NIRF and white light will be compared.
Time Frame
during surgery
Secondary Outcome Measure Information:
Title
Total surgical time
Time Frame
From incision until closure
Title
Histology: are parathyroid glands in the specimen? (as in standard care)
Description
immediately after surgery, the thyroid specimen will be send to the pathology department for histological examination as in standard care, with extra attention on wether there are parathyroid glands in the specimen.
Time Frame
assessment within 1 week after surgery
Title
Subjective opinion surgeon about the usefulness of the technique
Time Frame
Immediately after surgery
Title
Intra-operative complications due to the use of the technique
Time Frame
during surgery
Other Pre-specified Outcome Measures:
Title
Quantitative measurement of fluorescence signal related to parathyroid function
Description
Quantitative measurement of fluorescence signal using Target to Background Ratio (TBR) is used, combined with parameters of parathyroid function, namely Calcium levels postoperatively day 1 and day 2, and week 2 in patients after total thyroidectomy (as in standard care), and TSH in patients after total thyroidectomy 2 weeks postoperatively (as in standard care).
Time Frame
up to 2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female patients, aged 18 years and above Scheduled for elective total or hemi thyroidectomy Normal liver and renal function No known hypersensitivity for iodine or ICG Able to understand the nature of the study procedures Willing to participate and give written informed consent Exclusion Criteria: Age < 18 years Liver or renal insufficiency Known ICG, iodine, penicillin or sulfa hypersensitivity Pregnancy or breastfeeding Not able to understand the nature of the study procedure i.v. heparin injection in the last 24h (LMWH not contraindicated) Not willing to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole Bouvy, M.D. Ph.D.
Organizational Affiliation
Maastricht University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maastricht University Medical Center
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6202
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No

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NIRF for Parathyroid Visualization: a Pilot Study

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