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Autofluorescence vs Clinical Assessment of Parathyroid Glands During Thyroid Surgery

Randomized Controlled Trial of Fluobeam® LX Compared With Clinical Assessment of Parathyroid Glands to Counteract Postoperatively Failing Parathyroid Function With Low Blood Calcium After Thyroid Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04509011
Enrollment
516
Registered
2020-08-11
Start date
2021-01-05
Completion date
2023-07-31
Last updated
2024-11-15

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

Conditions

Hypoparathyroidism Postprocedural

Keywords

Hypoparathyroidism, PTH, Hypocalcemia

Brief summary

The purpose of the investigation is to study if the use of Fluobeam®-LX to identify parathyroid glands through autofluorescence during thyroid surgery, may reduce the risk of postoperative hypoparathyroidism, defined as low PTH in patients undergoing total thyroidectomy

Detailed description

Temporary and permanent hypoparathyroidism is probably the most important complication of total thyroidectomy. The rate of permanent hypoparathyroidism in quality registries are in the range of is 5-7 percent of patients undergoing surgery. Patients operated on benign disease with total thyroidectomy, and who suffer from permanent hypoparathyroidism (defined as medication with active Vitamin D analogue therapy for more than 6 months, are at increased risk of renal insufficiency. They also have, for unclear reasons, an increased risk of suffering from malignancy, compared to patients without this complication. Patients with known ischemic heart disease before surgery also have an increased risk of suffering a new episode of cardiovascular disease. Finally, patients with permanent hypoparathyroidism have an increased risk of mortality compared to patients without this complication. If, by using a technique for autofluorescence (Fluobeam® -LX), one can more accurately identify and avoid damage to the parathyroid glands during the surgical procedure, this would be of great importance for patients undergoing total thyroidectomy for thyroid disease. Patients undergoing total thyroidectomy are randomized to the use of Fluobeam® -LX to detect the parathyroid glands through autofluorescence during thyroid surgery, or clinical evaluation only (control). Outcome is evaluated by parathyroid hormon (PTH) levels the first postoperative day and the need for medication with calcium and Vitamin D up to 6 months postoperatively.

Interventions

DEVICEFluobeam® LX

Fluobeam®-LX is used to identify and evaluate parathyroid glands using auto-fluorescence during thyroid surgery.

Sponsors

Haukeland University Hospital
CollaboratorOTHER
Jagiellonian University
CollaboratorOTHER
Sahlgrenska University Hospital
CollaboratorOTHER
Hospital Rudolfstiftung
CollaboratorOTHER
Region Skane
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Masking description

The participant is not informed of the assigned group, whereas the the care giver (surgeon) is informed due to the use (or not) of the Fluobeam®-LX. Randomization is performed 1: 1 in blocks of 10 via the Eurocrine quality register platform.

Intervention model description

Intervention group (intraoperative use of Fluobeam®-LX during thyroid surgery) Control group (clinical assessment and identification of parathyroid glands during thyroid surgery)

Eligibility

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

Inclusion criteria

Patients with thyroid disease planned for total thyroidectomy regardless of diagnosis

Exclusion criteria

* Previous thyroid surgery * Previous parathyroid surgery * Concurrent parathyroid surgery * Renal insufficiency * Pregnancy * Breast feeding * Allergy (contrast agent, iodine) * Inability to understand study information * Patient unable to participate in planned follow-up program

Design outcomes

Primary

MeasureTime frameDescription
Postoperative level of Parathyroid hormone (PTH)First postoperative dayLow plasma parathyroid hormone (PTH) (below the normal reference range)

Secondary

MeasureTime frameDescription
Autotransplantation of parathyroid tissueIntraoperativelyNumber of autotransplanted parathyroid glands
Postoperative medication with Active vitamin DAt discharge (up to 7 days), at 1 month and at 6 monthsMedication with active Vitamin D; dihydrotachysterol (ATC A11CC02), alfacalcidol (ATC A11CC03), or calcitriol (ATC A11CC04) due to postoperative hypocalcaemia. Evaluated by standard questionaire in the database Eurocrine (yes/no)
Excised parathyroid glandsOne weekNumber of excised parathyroid glands found on the specimen at histopathology
Identification of parathyroid glandsIntraoperativelyNumber of identified parathyroid glands
Time for operationIntraoperativelyTime for surgery (skin to skin) in minutes
Hospital stayOne weekHospital stay in days
Re-hospitalization due to hypocalcaemiaOne monthAny subsequent hospitalization within 30 days for hypocalcaemia-related symptoms
Postoperative medication with oral calciumAt discharge (up to 7 days), at 1 month and at 6 monthsMedication with oral calcium; calcium carbonate (A12AA04), and calcium lactate gluconate (A12AA06) Evaluated by standard questionaire in the database Eurocrine (yes/no)

Countries

Austria, Norway, Poland, Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026