Actively Recruiting
Prophylactic Lymphovenous Bypass Procedure Following Inguinal Lymphadenectomy: A Prospective Observational Study
Led by M.D. Anderson Cancer Center · Updated on 2025-11-10
20
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To learn if LBP can help to prevent lymphedema when it is performed at the time of surgery rather than after a patient has already developed the disease.
CONDITIONS
Official Title
Prophylactic Lymphovenous Bypass Procedure Following Inguinal Lymphadenectomy: A Prospective Observational Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older
- Patients willing to participate
- Patients able to provide informed consent
- Patients undergoing inguinal lymphadenectomy (ILND)
You will not qualify if you...
- Taking anticoagulant medications within 7 days before surgery
- Known pregnancy at the time of surgery
- Unavailable for follow-up less than 18 months or missing scheduled measurements
- Body mass index (BMI) greater than 50.0
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
A
Ashleigh Francis, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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