Immediate Lymphatic Repair at Lymph Node Surgery for Melanoma Patients
Official title: Immediate Lymphatic Reconstruction After Lymphadenectomy in Melanoma Patients: a Parallel Cohort Pilot Study
Run by M.D. Anderson Cancer Center · NCT06887205 · Data updated 2026-11-12
This study tests whether doing a lymphovenous bypass during lymph node removal for melanoma can help prevent lymphedema and improve recovery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | June 10, 2026 |
| Main results expected | September 1, 2028 |
| Study ends | September 1, 2028 |
| Registry record updated | June 18, 2026 |
| Trial ID | NCT06887205 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with melanoma undergoing axillary or inguinal lymph node dissection who consent to participate and can complete assessments.
✕Probably not a fit
Patients with BMI >50, current pregnancy, recent use of anticoagulants, or other contraindications may not benefit or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional pilot study looks at performing lymphovenous bypass at the time of axillary or inguinal lymph node dissection in melanoma patients. It will measure how often lymphedema occurs within the first year after surgery, plus wound complications in 30 days, drain removal timing, and patient-reported quality of life. The study tracks LE prevalence at 3, 6, and 12 months, and estimates the time to first LE and cumulative incidence. LYMQOL is used to assess survivorship and lifestyle impact during follow-up.
Why it matters
Potential benefit: If successful, this approach could reduce the risk and impact of lymphedema after lymph node surgery in melanoma patients.
How similar studies have gone: Prior lymphedema prevention strategies have shown promise in other settings, but this parallel-cohort pilot explores a novel timing of LVB at surgery in melanoma.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Participants greater than or equal to 18 years of age. 2. Participants willing to participate. 3. Participants able to complete informed consent. 4. Participants with a diagnosis of Melanoma undergoing ALND or ILND. Exclusion Criteria: 1. Participant staking anticoagulants within 7 days prior to surgery. 2. Participants that are known to be pregnant at the time of surgery. 3. Participants with BMI greater than 50.0
Where it's running
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MD Anderson Cancer Center
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Ashleigh M Francis, MD — M.D. Anderson Cancer Center
- Study coordinator: Ashleigh M Francis, MD
- Email: amfrancis@mdanderson.org
- Phone: (713) 413-7451
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.