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Diagnostic Accuracy Study of Indocyanine Green for Parathyroid Perfusion Assessment

Diagnostic Accuracy Study of Indocyanine Green for Parathyroid Perfusion Assessment

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03969108
Enrollment
10
Registered
2019-05-31
Start date
2019-08-06
Completion date
2019-11-13
Last updated
2020-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Graves Disease, Thyroid Cancer, Thyroid Goiter

Keywords

Thyroid surgery, Indocyanine green (ICG), Hypoparathyroidism

Brief summary

This study aims to develop a standardized universal imaging protocol for ICG-guided fluorescent total thyroidectomy, including quantitative evaluations of the fluorescent signal. Therefore, patients will undergo thyroid surgery (total thyroidectomy) with the use of ICG fluorescence.

Detailed description

Background Thyroid surgery volume continues to increase worldwide over the past few decades. During a total thyroidectomy (TTx), the ultimate goal is to remove all thyroid tissue, whereas damage to adjacent tissue is prevented. However, iatrogenic hypoparathyroidism, as a result of surgical removal or damage to the parathyroid glands, occurs in approximately 30% of the cases. In 2016 near-infrared fluorescence guided surgery with indocyanine green (ICG) was proposed for visualizing viability and blood supply of parathyroid glands during TTx. ICG can visualize tissue perfusion, since it becomes completely and permanently fixed to plasma proteins once in the bloodstream, and circulates in the intravascular compartment only. However, one of the limitations of ICG imaging is the subjectivity of the interpretation of fluorescence, which makes the assessment of images inconsistent among studies. There is a clear need for standardization of the evaluation of the perfusion with ICG, since visual evaluation of the fluorescent signal of ICG is not sufficient to reliably predict the perfusion of parathyroid glands. Main research question To develop a standardized universal imaging protocol for ICG-guided fluorescent total thyroidectomy including quantitative evaluations of the fluorescent signal. Design This will be a proof-of-concept , prospective cohort study of patients undergoing a total thyroidectomy with ICG-guided fluorescent surgery to evaluate tissue perfusion The main study endpoint is quantification of the fluorescent signal of ICG. Secondary outcomes are data from surgery, postoperative lab values (including calcium, PTH, albumin) and postoperative medication use.

Interventions

DRUGIndocyanine Green

ICG is a fluorescent dye which binds tightly to plasma proteins and becomes confined to the vascular system.

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients ≥ 18 years 2. Patients undergoing total thyroidectomy as surgical procedure for thyroid cancer, Graves' disease or goiter 3. Patients are eligible for surgery 4. Patients are mentally competent and are able and willing to comply with study procedures 5. Written informed consent

Exclusion criteria

1. Patients with a known allergy to ICG or iodinated contrast 2. Pregnant or lactating women 3. Patients with previous neck surgery

Design outcomes

Primary

MeasureTime frameDescription
Quantification of the fluorescent signal of ICGAt time of surgeryQuantification of the fluorescent signal of ICG

Secondary

MeasureTime frameDescription
Duration of surgeryFrom start to end of surgeryDuration of surgery in minutes
Postoperative calcium concentrationPostoperative day 1 and at the first out-patient clinic visit (between 2 to 30 days postoperative)Postoperative albumin-corrected calcium concentration in blood
Appearance of parathyroid glandAt time of surgeryVascularization appearance of parathyroid gland intraoperatively (1= surgeon thinks parathyroid gland is well vascularized, 2 = surgeons thinks parathyroid gland is devascularized)
Rate of prescribed postoperative calcium medicationPostoperative day 1 and at the first out-patient clinic visit (between 2 to 30 days postoperative)Rate of prescribed postoperative calcium medication
Rate of prescribed postoperative vitamin D medicationPostoperative day 1 and at the first out-patient clinic visit (between 2 to 30 days postoperative)Rate of prescribed postoperative vitamin D medication
Postoperative PTH concentrationPostoperative day 1 and at the first out-patient clinic visit (between 2 to 30 days postoperative)Postoperative PTH concentration in blood

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026