Clinical trial · Interventional
Pedicled Lateral Chest Wall Lymph-Adipofascial Flap to Prevent Arm Lymphedema After Breast Cancer Surgery
Efficacy and Safety of Pedicled Lateral Chest Wall Lymph-Adipofascial Flap Axillary Reconstruction for the Prevention of Breast Cancer-Related Arm Lymphedema: A Prospective, Single-Arm, Phase II Clinical Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Breast cancer surgery that includes removal of lymph nodes from the armpit (axillary lymph node dissection) can disrupt normal lymphatic drainage and may lead to arm swelling, known as lymphedema. This condition can cause discomfort, limit arm function, and reduce quality of life. Patients with a higher body mass index and those who receive regional lymph node radiation are at particularly high risk. This study aims to evaluate whether a preventive surgical technique, called axillary reconstruction using a pedicled lateral chest wall lymph-adipofascial flap, can reduce the risk of developing arm lymphedema after breast cancer surgery. During standard breast cancer surgery with axillary lymph node dissection, a small flap of tissue containing fat, fascia, and lymphatic tissue from the lateral chest wall is rotated into the axillary area to fill the surgical space and support lymphatic drainage. This is a prospective, single-arm Phase II clinical study. Participants will be followed for up to 24 months after surgery to assess the occurrence of arm lymphedema, changes in arm volume and bioimpedance measurements, quality of life, and surgery-related complications. The results of this study may help determine whether this simple and widely applicable technique can safely reduce the risk of lymphedema in high-risk breast cancer patients.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Breast Cancer-Related Lymphedema | — | UNRESOLVED | — |
| Postoperative Complications | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pedicled Lateral Chest Wall Lymph-Adipofascial Flap Axillary Reconstruction | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Pedicled Lymph-Adipofascial Flap Axillary Reconstruction
- description
- Participants in this arm will undergo standard breast cancer surgery with axillary lymph node dissection, followed by immediate axillary reconstruction using a pedicled lateral chest wall lymph-adipofascial flap. The flap, containing adipose tissue, deep fascia, and lymphatic structures, is harvested from the lateral chest wall and rotated into the axillary defect without microsurgical anastomosis. This preventive surgical approach is intended to support lymphatic drainage and reduce the risk of postoperative arm lymphedema.
- interventionNames
- Procedure: Pedicled Lateral Chest Wall Lymph-Adipofascial Flap Axillary Reconstruction
Primary outcomes (1)
- measure
- Lymphedema-Free Survival of the Operated Arm
- timeFrame
- Up to 24 months after surgery
- description
- The primary outcome is the proportion of participants who remain free of arm lymphedema after surgery. Arm lymphedema is defined by the presence of clinical symptoms or signs consistent with lymphedema together with objective measurement criteria, including a relative volume change of the operated arm or abnormal bioimpedance measurements, as assessed during follow-up.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Female patients aged 18 to 75 years; 2. Histologically confirmed invasive breast cancer; 3. Pathologically confirmed axillary lymph node metastasis requiring axillary lymph node dissection; 4. Body mass index (BMI) ≥ 25 kg/m²; 5. Planned to receive postoperative regional lymph node radiation therapy; 6. Ability to understand the study procedures and provide written informed consent; 7. Willingness and ability to comply with study follow-up and assessments. Exclusion Criteria: 1. Previous surgery involving the ipsilateral axilla; 2. Previous radiation therapy to the ipsilateral axilla; 3. Evidence of distant metastatic breast cancer; 4. Bilateral breast cancer, or a history of contralateral breast cancer surgery; 5. Severe hepatic or renal dysfunction, or severe cardiac insufficiency; 6. Inability to read or understand Chinese sufficiently to complete study questionnaires and assessments; 7. Pregnancy; 8. Any condition or circumstance that, in the investigator's judgment, may interfere with study compliance or follow-up.
References
Publications (0)
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