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Clinical Trials/NCT01598727
NCT01598727CompletedPhase 1

A Phase I Feasibility Study of Intra-operative Near Infra-red Fluorescent Imaging in Thyroid/Parathyroid Surgery With the Fluobeam(TM) System of Fluoptics

Sheffield Teaching Hospitals NHS Foundation Trust1 site in 1 country10 target enrollmentStarted: July 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Determine patterns of fluorescence from soft tissue structures in the neck

Study Overview

Brief Summary

Hypothesis: Intraoperative use of near infrared fluorescent imaging technology and detection of Methylene Blue fluorescence will improve outcomes following thyroid and parathyroid surgery.

Aims: The aims of this phase of the study are to determine the feasibility of using near infrared fluorescent technology in the detection of parathyroid tissue and its differentiation from adjacent soft tissue during surgery on parathyroid glands.

Objectives of the phase I study:

  1. To familiarise surgical teams with the intraoperative use of the 'Fluobeam(TM)' device (Fluoptics).
  2. To understand the patterns (onset, intensity and duration) of fluorescent staining of normal parathyroid glands, thyroid glands and other soft tissue structures encountered during parathyroidectomy.

Further research:

This will be followed by a phase II study during which fluorescent imaging will be used in conjunction with intraoperative incremental dose of IV methylene blue in both thyroid and parathyroid surgery. Phase II will enable us to develop a protocol for the use of a minimum possible dose of MB for the identification of parathyroid glands. This will then be tested in the pilot phase of a randomized clinical trial.

Detailed Description

As above

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •all patients undergoing parathyroid surgery

Exclusion Criteria

  • •patients undergoing re-do procedures
  • •patients unable to give adequate informed consent
  • •patients with a history of intolerance or sensitivity to MB
  • •patients with G6PD deficiency
  • •patients on serotonin reuptake inhibitors and patients undergoing thoracic exploration
  • •either alone or in combination with a neck exploration.

Arms & Interventions

Fluobeam(TM) Imaging System (Fluoptics)

Experimental

Single arm observational pilot study

Intervention: Fluobeam(TM) Imaging System (Fluoptics) (Device)

Outcomes

Primary Outcomes

Determine patterns of fluorescence from soft tissue structures in the neck

Time Frame: 1 Day

This is a proof of principle study aimed to demonstrate that the patterns of Methylene Blue emitted fluorescence from the parathyroid glands, thyroid glands and other soft tissue structures in the neck such as lymph glands are distinct and can be used to differentiate between them at surgery. The fluorescence from the various structures will be recorded as 'no', 'mild' and 'yes'.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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