Completed

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

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What is being tested

Fluobeam® LX

Device
Who is being recruted

Calcium Metabolism Disorders+5

+ Endocrine System Diseases

+ Hypocalcemia

Over 18 Years
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: January 2021
See protocol details

Summary

Principal SponsorRegion Skane
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 5, 2021

Actual date on which the first participant was enrolled.

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.

Official TitleRandomized 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
NCT04509011
Principal SponsorRegion Skane
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

516 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Calcium Metabolism DisordersEndocrine System DiseasesHypocalcemiaHypoparathyroidismMetabolic DiseasesNutritional and Metabolic DiseasesParathyroid DiseasesWater-Electrolyte Imbalance

Criteria

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

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Fluobeam® LX is used to detect autofluorescens and identify and evaluate parathyroid glands

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 5 locations

Suspended

Rudolfstiftung

Vienna, AustriaOpen Rudolfstiftung in Google Maps
Suspended

Haukeland University Hospital

Bergen, Norway
Suspended

Jagiellonian University Medical College

Krakow, Poland
Suspended

Sahlgrenska University Hospital

Gothenburg, Sweden
Completed5 Study Centers