Fibrin Melanoma Axillary Node Study in Patients With Melanoma

Melanoma Clinical Trial

Official title:

A Randomized Trial Evaluating the Use of Fibrin Tissue Adhesive Following Axillary Node Dissection in Patients With Melanoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00504582
• Other study ID #: GS01-565
• Secondary ID: NCI-2012-01524
• Status: Completed
• Phase: N/A
• Start date: May 15, 2002
• Est. completion date: April 9, 2020

Study information

• Verified date: April 2023
• Source: M.D. Anderson Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary Objective:

• To determine whether the use of a fibrin sealant applied to axillary soft tissues following node dissection can result in earlier drain removal.

Secondary Objectives:

• To determine the postoperative morbidity rate using fibrin sealant following axillary node dissection.

• To assess patient-valuation of outcome by performing a cost-benefit analysis using a willingness-to-pay model.

• To determine if serum levels, lymphatic fluids level, or cutaneous expression of vascular endothelial growth factor-D (VEGF-D), vascular endothelial growth factor-C (VEGF-C) or their receptor, vascular endothelial growth factor receptor-3 (VEGFR-3) correlates with nodal tumor burden or development of lymphedema in patients with melanoma.

Description:

Patients in this study are scheduled to have axillary node dissection as part of their surgery for treatment of their melanoma.

Within 2 weeks before entry into the study, patients will have a complete physical exam and medical history.

These patients will be randomly assigned (as in the toss of a coin) to one of two groups. Patients in one group will receive TISSEEL applied externally to the dissected axillary area. Patients in the other group will receive no fibrin sealant.

For patients who are admitted to the hospital, the surgical site will be monitored by the surgeon for evidence of wound complications in the first 24 hours after surgery. At the time of discharge from the hospital, patients will be instructed in drain care and how to measure the drainage each day until the drain is removed.

The contents of the drain will be collected from patients during the first day after surgery, during the first return follow-up visit to M.D. Anderson Cancer Center, and during drain removal (unless these latter 2 dates are the same).

Follow-up wound exams will be performed by the local primary physician or in the M.D. Anderson Melanoma Clinic between 1-4 weeks and 6 weeks after surgery. Participation will be over at the 6-week follow-up.

THIS IS AN INVESTIGATIONAL STUDY. The sealant is FDA approved, though its use in this study is experimental. About 115 patients will take part in this study. All will be enrolled at M. D. Anderson.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 121
• Est. completion date: April 9, 2020
• Est. primary completion date: April 9, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Part I - Inclusion Criteria, patients that consent to participate.

2. Patients with melanoma who have undergone axillary dissection within the last six months as part of their surgical treatment will be considered for the study.

Exclusion Criteria:

1. Part II - Exclusion Criteria, patients with known hypersensitivity to bovine proteins.

2. Patient has undergone prior radiation therapy to the operative site.

3. Patient is pregnant or lactating.

4. Patient is steroid dependent within prior 6 months.

5. Patient has used aspirin or other anti-platelet drug (excluding Celebrex) within seven days of operation.

6. Patient has pre-existing lymphedema.

7. Patient has other pre-existing medical conditions with evidence of organ dysfunction as determined by principal investigator.

Related Conditions & MeSH terms

• Melanoma

Intervention

Drug:
• Fibrin Sealant
Tisseel applied externally to the dissected axillary area.

Locations

Country	Name	City	State
United States	University of Texas MD Anderson Cancer Center	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Drain Duration	Number of days drain was in place	from surgery until drain removed, up to 40 days
Secondary	Number of Participants With Infection	Number of participants with any signs of infection noted following surgery requiring intervention.	after surgery until the wound is healed, up to 30 days whichever is longer

External Links

•   University of Texas MD Anderson Cancer Center Website