Skip to content

Evaluation of the Interest of the Medical Device Called "Fluobeam" in the Localization, Visualization of the Parathyroid Glands for Patients With Mild Primary Hyperparathyroidism

Evaluation of the Interest of the Medical Device Called "Fluobeam" in the Localization, Visualization of the Parathyroid Glands for Patients With Mild Primary Hyperparathyroidism. A Randomized Controled Prospective Open -Labeled Monocentric Study.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03643081
Acronym
FLUO-PARA
Enrollment
132
Registered
2018-08-22
Start date
2018-12-20
Completion date
2024-01-08
Last updated
2026-09-14

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

Conditions

Mild Primary Hyperparathyroidism

Brief summary

The aim of our study is to evaluate the value of the camera called "Fluobeam" in the localization, visualization of the parathyroid glands for patients with mild primary hyperparathyroidism.

Detailed description

Recently, it has been shown that parathyroid glands presented auto fluorescence, visible in the near infra-red light. Parathyroid glands emit at 822 nanometers when they are stimulated by a laser of 785 nanometers. Fluoptics Company (Fluoptics SAS, Grenoble, France) will provide a camera called "Fluobeam", facilitating the visualization of the parathyroid glands. The fluorescence intensity of the parathyroid glands is much more elevated than that of the surrounding tissues. Preliminary work showed the interest of this technique. Benmiloud and collabortors have shown that the utilization of the "Fluobeam" enable to decrease the post total thyroidectomy hypocalcemia rate by a better visualization and preservation of the parathyroid glands. The aim of this study is to evaluate the value of "Fluobeam" in the localization, visualization of the parathyroid glands for patients with mild primary hyperparathyroidism.

Interventions

DEVICEUse of the camera "Fluobeam"

Use of the camera "Fluobeam" to localize, visualize the parathyroid glands during a parathyroidectomy.

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Adult between 18 and 80 years old. * Given signed written informed consent. * Patient with moderated and sporadic primary hyperparathyroism (albumin-corrected serum calcium ≤2.85 mmol/l) requiring to be operated on. * Patient affiliated to a social security system.

Exclusion criteria

* Underage and adults under guardianship. * Pregnant or breast feeding women. * Patients with history of cervical radiotherapy or cervicotomy.

Design outcomes

Primary

MeasureTime frame
To compare the time required for the parathyroidectomy with or without the utilization of the camera "Fluobeam".At Day 1(parathyroidectomy)

Secondary

MeasureTime frameDescription
To compare the results of the parathyroidectomy with or without the utilization of the camera "Fluobeam" in term of biological recovery.At 6 months post parathyroïdectomyTo compare the results of the parathyroidectomy with or without the utilization of the camera "Fluobeam" in term of biological recovery determined by normocalcemia (2,20 mmol/L \< calcium \< 2,60 mmol/L) at 6 months post surgery.
To compare the results of the surgery with or without the utilization of the "Fluobeam" in term of number of visualized parathyroid glands.At Day 1(parathyroidectomy)
To compare the results of the surgery with or without the utilization of the "Fluobeam" in term of post-surgery laryngeal paralysis.At 6 months post parathyroïdectomy
To compare the results of the surgery with or without the utilization of the "Fluobeam" in term of parathyroid morbidity (hypocalcemia with calcémia below 2 mmol/L)At 6 months post parathyroïdectomy
To compare the results of the surgery with or without the utilization of the "Fluobeam" in term of cost-utility analysis according to the societal perspective and over a 6 months' time horizon of the surgery.At 6 months post parathyroïdectomy

Countries

France

Contacts

PRINCIPAL_INVESTIGATOREric MIRALLIE, Pr

Nantes University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026