Proof-of-concept Study of LymphMonitor 1.0 to Assess the Lymphatic Vessel Function

NCT ID: NCT04393168

Last Updated: 2020-07-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-05-22
• Study Completion Date: 2020-06-26

Brief Summary

Lymphedema is the consequence of injured lymphatic system and is characterized by chronic, often disabling swelling of am affected body part, often arm or leg. In the western world secondary lymphedema arises most commonly after removal lymph nodes in an operation as a part of cancer treatment (for example from the armpits or the groin region), however it may also develop as a result of radiation, any other operation, infection or injury that destroys a part of lymphatic system. The disease often develops even years after the event. While there is no cure for lymphedema at present, early detection would ensure timely physiotherapy and application of compression garments that significantly slow down or stop the progression of the disease. However, presently used methods of that are used for diagnosis and evaluating the stage of the disease, are either invasive and expensive or inaccurate and can only be performed at specialized medical centres.

Therefore, we developed a simple, affordable and accurate technology, LymphMonitor 1.0 that can allow for testing how efficiently the lymphatic system is functioning. The test can be performed at the local medical centre or potentially even at home.

In this study, we investigate whether LymphMonitor 1.0 technology can distinguish between a healthy and a diseased lymphatic system (in lymphedema). This method may allow early diagnosis of lymphedema so that the development of the disease can be detected and prevented early enough. By participating in the study the lymphedema patients are making an important contribution to increasing the quality of life of lymphedema patients. In LymphMonitor 1.0 method method, a solution of a safe fluorescent dye, indocyanine green, is injected painlessly using tiny microneedles, MicronJet600TM, directly into the skin of the arm or leg. After injection, this dye is removed from the skin only through the lymphatic vessels. The intensity of the fluorescence signal corresponds to the amount of dye left in the skin. The decrease in the fluorescence signal after the injection is measured on the surface on the skin using a new device, LymphMeter 1.0. The faster the dye (and that fluorescence signal) disappears from the surface of the skin, the better the lymphatic system works. Therefore in the arm or leg affected by lymphedema the fluorescence signal will decrease much slower compared to the healthy one.

Conditions

Lymphedema; Secondary Lymphedema

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Patients with unilateral arm or leg lymphedema

Group Type: EXPERIMENTAL

Lymphatic clearance measurement

Intervention Type: COMBINATION_PRODUCT

The indocyanine green in 5% human albumin solution (tracer) (50 μL) will be injected intradermally in both forearms or both lower legs using MicronJet600 microneedles paying attention to the contralateral symmetry of the injections. The signal at the injection sites will be measured over time using a hand-held portable device LymphMeter 1.0 for the total duration of 3 h. In the first hour, the signal will be measured every 15 minutes followed by measurements every half an hour. Immediately after injection (t=0 h), 1.5 h and 3 h after injection the skin area occupied by the tracer will be measured using a standard near-infrared camera, Fluobeam. The dermal reaction at the injection site will be assessed by observations for presence of redness/erythema and measuring its extent according to the needs. The patient will be constantly observed for the signs of allergic reactions, skin irritations or intolerances.

Interventions

Lymphatic clearance measurement

The indocyanine green in 5% human albumin solution (tracer) (50 μL) will be injected intradermally in both forearms or both lower legs using MicronJet600 microneedles paying attention to the contralateral symmetry of the injections. The signal at the injection sites will be measured over time using a hand-held portable device LymphMeter 1.0 for the total duration of 3 h. In the first hour, the signal will be measured every 15 minutes followed by measurements every half an hour. Immediately after injection (t=0 h), 1.5 h and 3 h after injection the skin area occupied by the tracer will be measured using a standard near-infrared camera, Fluobeam. The dermal reaction at the injection site will be assessed by observations for presence of redness/erythema and measuring its extent according to the needs. The patient will be constantly observed for the signs of allergic reactions, skin irritations or intolerances.

Intervention Type: COMBINATION_PRODUCT

Eligibility Criteria

Inclusion Criteria

• informed consent as documented by signature
• females and males 18 - 75 years old,
• established (stage 2 or higher) unilateral secondary arm or leg lymphedema resulting from lymphadectonomy, radiation or any other surgical treatment, infection or injury.
• good general health status.

Exclusion Criteria

• critical illness (active cancer, renal failure, hepatic dysfunction)
• active infection
• blood vascular malformations or diseases
• scleroderma
• primary lymphedema
• patients who underwent any surgical procedures for treatment of lymphedema (e.g. lymphovenous anastomosis, liposuction, lymph node transfer).
• contraindications to use ICG (VERDYE), i.e.
• patients with hypersensitivity to ICG or to sodium iodide
• patients with hypersensitivity to iodine,
• patients with hyper-thyroidism, patients with autonomic thyroid adenomas
• patients in which the injection of VERDYE was poorly tolerated in the past it must not be used again, since severe anaphylactic reactions might occur.
• hypersensitivity to albumin or its excipients
• women, who are pregnant (pregnancy test will be performed in case of women who did not undergo menopause),
• women who are breast feeding ,
• enrolment of the investigator, his/her family members, employees and other dependent persons,
• known or suspected non-compliance, drug or alcohol abuse,
• inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant,
• participation in another study with investigational drug within the 30 days preceding and during the present study,
• previous enrolment into the current study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Swiss Federal Institute of Technology

OTHER

Sponsor Role: collaborator

Zurich University of Applied Sciences

OTHER

Sponsor Role: collaborator

University Hospital, Zürich

OTHER

Sponsor Role: collaborator

NanoPass Technologies Ltd

INDUSTRY

Sponsor Role: collaborator

Nicole Lindenblatt

OTHER

Sponsor Role: lead

Responsible Party

Nicole Lindenblatt

Deputy Director of the Division of Plastic and Hand Surgery

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Nicole Lindenblatt, M.D, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hostpial Zurich

Locations

University Hostpial Zurich

Zurich, , Switzerland

Countries

Switzerland

Other Identifiers

2019-01823

Identifier Type: REGISTRY

Identifier Source: secondary_id

POCLymphMonitor 1.0

Identifier Type: -

Identifier Source: org_study_id