Skin sensation and quality of life in breast cancer-associated lymphedema

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400081860

Enrollment

Unknown

Registered

2024-03-14

Start date

2024-03-15

Completion date

Unknown

Last updated

2024-07-08

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

Conditions

Lymphedema

Interventions

Experimental group:2-week CDT comprehensive treatment

Control group :two weeks of regular intervention, including functional exercise, skin care, avoiding overwork, avoiding wounds, and other measures.

Eligibility

Sex/Gender

All

Age

18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of lymphedema 2.Age 18-79 years 3.Signed informed consent

Exclusion criteria

Exclusion criteria: 1.Severe cardiac and renal insufficiency 2.Recurrence or metastasis 3.Cognitive impairment

Design outcomes

Primary

Measure	Time frame
Body circumference;Sensory measurement;	—

Secondary

Measure	Time frame
Quality of life;	—

Countries

China

Contacts

Public ContactSong Yufeng

The Second Hospital of Shanxi Medical University

songyufeng2010@sohu.com+86 136 3347 5405

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026