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Completed

NCT Number: NCT04509011

Autofluorescence vs Clinical Assessment of Parathyroid Glands During Thyroid Surgery

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rudolfstiftung, Vienna, Austria

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Fluobeam® LX

Device

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

Primary outcomes

  1. Postoperative level of Parathyroid hormone (PTH)

    Time frame: First postoperative day

    Low plasma parathyroid hormone (PTH) (below the normal reference range)

Secondary outcomes

  1. Postoperative medication with Active vitamin D

    Time frame: At discharge (up to 7 days), at 1 month and at 6 months

    Medication 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)

  2. Postoperative medication with oral calcium

    Time frame: At discharge (up to 7 days), at 1 month and at 6 months

    Medication with oral calcium; calcium carbonate (A12AA04), and calcium lactate gluconate (A12AA06) Evaluated by standard questionaire in the database "Eurocrine" (yes/no)

  3. Identification of parathyroid glands

    Time frame: Intraoperatively

    Number of identified parathyroid glands

  4. Autotransplantation of parathyroid tissue

    Time frame: Intraoperatively

    Number of autotransplanted parathyroid glands

  5. Excised parathyroid glands

    Time frame: One week

    Number of excised parathyroid glands found on the specimen at histopathology

  6. Time for operation

    Time frame: Intraoperatively

    Time for surgery (skin to skin) in minutes

  7. Hospital stay

    Time frame: One week

    Hospital stay in days

  8. Re-hospitalization due to hypocalcaemia

    Time frame: One month

    Any subsequent hospitalization within 30 days for hypocalcaemia-related symptoms

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Collaborators

  • Haukeland University Hospital
  • Hospital Rudolfstiftung
  • Jagiellonian University
  • Sahlgrenska University Hospital

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2022
Study completion
2023
First posted
Aug 11, 2020
Registry last updated
Nov 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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