Early Diagnosis of Breast Cancer-related Lymphedema

NCT ID: NCT06046365

Last Updated: 2025-06-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-24

Study Completion Date

2026-12-31

Brief Summary

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This study will conduct clinical trials to explore the mechanisms behind the development of upper limb lymphedema following breast cancer surgery. The investigators will recruit patients who have undergone breast cancer surgery and utilize Indocyanine Green (ICG) lymphography and Lymphoscintigraphy to identify the locations of lymphatic blockages. Shear Wave Elastography (SWE) will be used to detect changes in tissue limb compliance. DXA body composition analysis will measure the differences in the composition ratios between edematous and normal limbs. In addition, diffusion correlation spectrometry will be employed to monitor changes in deep tissue blood flow, complemented by continuous measurements of limb circumference and other physiological parameters. The study aims to explore the interrelationships among lymphatic circulation, limb circumference, tissue compliance, and tissue blood flow rates.

Detailed Description

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Breast cancer ranks as the most common cancer among women in Taiwan. According to the cancer registry data of Taiwan's Ministry of Health and Welfare, there were 16,325 new cases of breast cancer in 2016. Approximately one in 12 women will develop breast cancer in her lifetime. Although the incidence rate is high, the survival rate after clinical treatment is also quite high. The five-year survival rate for early-stage breast cancer patients exceeds 90%, making it a highly manageable disease at present.

The incidence rate of breast cancer-related lymphedema is around 21.4%, and is expected to become increasingly common as the survival rate of patients improves. Aside from causing psychological distress, it also impairs a patient's work and daily life capabilities. Patients also have to bear additional medical expenses, which brings a significant financial burden to families. Current research supports that early detection and treatment are key to controlling breast cancer-related lymphedema. However, there is still a need for a clearer understanding of the risk factors causing lymphedema and the physiological changes that occur when it manifests, in order to achieve the goal of early detection.

This study will conduct clinical trials to investigate the mechanisms of upper limb lymphedema after breast cancer surgery. The investigators will recruit post-operative breast cancer patients and use Indocyanine Green (ICG) lymphography and Lymphoscintigraphy to detect lymphatic blockage locations; Shear Wave Elastography (SWE) to detect changes in tissue limb compliance; DXA body composition analysis to measure the differences in edema and normal limb composition ratios; and diffusion correlation spectrometry to measure deep tissue blood flow changes, along with continuous measurements of limb circumference and other physiological parameters. The study aims to explore the interrelationship among lymphatic circulation, limb circumference, tissue compliance, and tissue blood flow.

The expected results of this study can help the investigators understand the risk factors causing lymphedema and the physiological changes that occur when it manifests, overcome the current difficulties in early lymphedema detection, and develop effective monitoring methods and equipment. This will provide more possibilities for the early detection and treatment of future patients with breast cancer-related lymphedema.

Conditions

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Lymphedema

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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mastectomy

Expected to include female patients who are undergoing breast cancer resection surgery or those who have already undergone breast resection surgery for breast cancer.

lymphoscintigraphy

Intervention Type DIAGNOSTIC_TEST

lymphoscintigraphy

circumference measurement

Intervention Type DIAGNOSTIC_TEST

circumference measurement

sonography

Intervention Type DIAGNOSTIC_TEST

B-mode sono and elastography

DXA body composition analysis

Intervention Type DIAGNOSTIC_TEST

DXA body composition analysis

Interventions

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lymphoscintigraphy

lymphoscintigraphy

Intervention Type DIAGNOSTIC_TEST

circumference measurement

circumference measurement

Intervention Type DIAGNOSTIC_TEST

sonography

B-mode sono and elastography

Intervention Type DIAGNOSTIC_TEST

DXA body composition analysis

DXA body composition analysis

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Female patients who are expected to undergo breast cancer resection surgery or have already undergone breast resection surgery for breast cancer.
* Absence of unhealed open wounds or other conditions unsuitable for tactile measurements within the measurement area.
* No severe cognitive or emotional impairments.
* No substance abuse (alcohol or drugs).
* Females aged between 20 and 80, capable of fully complying with the requirements of this study plan.

Exclusion Criteria

* Presence of unhealed open wounds or other conditions unsuitable for tactile measurements within the measurement area.
* Upper limb abnormalities in function (including joint mobility and muscle strength).
* Significant cognitive, auditory, or expressive language issues that hinder comprehension and compliance with instructions.
* Lack of assistance for daily measurements.
Minimum Eligible Age

20 Years

Maximum Eligible Age

80 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Kaohsiung Veterans General Hospital.

OTHER

Sponsor Role lead

Responsible Party

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Zheng-Yu Hoe, MD., PhD.

Chairperson

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kaohsiung Veterans General Hospital

Kaohsiung City, , Taiwan

Site Status RECRUITING

Countries

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Taiwan

Central Contacts

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Zheng Yu Hoe

Role: CONTACT

+886935517631

Facility Contacts

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Zheng-Yu Hoe

Role: primary

+886975581721

Other Identifiers

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22-CT2-15(211230-3)

Identifier Type: -

Identifier Source: org_study_id

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