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Pycnogenol for the Treatment of Lymphedema of the Arm in Breast Cancer Survivors

Primary Purpose

Lymphedema, Breast, Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Pycnogenol
Sponsored by
National Center for Complementary and Integrative Health (NCCIH)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphedema focused on measuring lymphedema, breast, cancer, plant preparation, herbal preparation, pine bark extract

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: Unilateral (ipsilateral to breast cancer resection side) lymphedema of the upper extremity. Extravascular water ration of > 1.07/1 between affected vs. normal arm using multiple frequency bioelectric impedence Patient is > 2months from last surgical or radiation treatment to the affected axilla Renal and hepatic function: Creatinine clearance > 50ml/min, total bili <2 mg/dl, transaminases <1.5 x ULN Patient not pregnant or breastfeeding. Use of barrier contraception if sexually active. ECOG performance of 0-2 Patient not allergic to pycnogenol Exclusion criteria: Patients treated with their first course of chemotherapy or radiation Chemotherapy or radiation to axillary lymph node will exclude patients for 8 weeks following treatment Patients with more than one episode of arm cellulitis, venous clot, or woody fibrosis of the affected arm. Antibiotics used to treat cellulitis must be completed at least 4 weeks prior to initial screening Patients with a defibrillator Midazolam study only: Patients requiring or benefiting from supplemental oxygen, patients allergic to cherries

Sites / Locations

  • University of Wisconsin Comprehensive Cancer Center and School of Pharmacy

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
July 14, 2003
Last Updated
April 21, 2008
Sponsor
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00064857
Brief Title
Pycnogenol for the Treatment of Lymphedema of the Arm in Breast Cancer Survivors
Official Title
Pycnogenol for the Treatment of Lymphedema of the Arm in Breast Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
April 2008
Overall Recruitment Status
Completed
Study Start Date
August 2003 (undefined)
Primary Completion Date
August 2007 (Actual)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to evaluate the effectiveness of a standardized botanical extract of Pycnogenol as a treatment for stable arm lymphedema in breast cancer survivors.
Detailed Description
Lymphedema of the arm affects the function and self-image of approximately 600,000 of the 2 million breast cancer survivors in the United States. Chronic lymphedema can lead to recurrent infections and permanent swelling, in some cases impairing function. Although various methods of massage and the use of non-elastic compression "sleeves" have been shown to decrease the severity of lymphedema, these methods of physical therapy are limited in terms of patient acceptance, compliance, and by the availability of trained therapists. There is presently no pharmacologic treatment that has proven effective in treating or preventing the development of lymphedema in women treated for breast cancer. This is a double-blind, placebo-controlled trial of an extract of the bark of the French maritime pine tree (Pycnogenol(r)) as a treatment for arm lymphedema in breast cancer survivors. Pycnogenol(r) is widely used in Europe for lymphedema of the leg and varicose veins, and is thought to act by several mechanisms including vascular permeability and vascular constriction. The development of such a therapeutic approach would therefore constitute a major breakthrough in the treatment of this common symptom of breast cancer lymphedema. Bioelectric impedance is a painless, quick, and easily-performed method of estimating the extracellular and total water volume of the body or segment, such as the arm. We will compare the correlation of both a single- and a multiple-frequency bioelectric impedance instrument in measuring change in arm volume to a standard assessment using water displacement. We expect that bioelectric impedance will prove faster and more sensitive to changes in extracellular water (lymphedema) than the water displacement method. We also propose to use a small oral dose of midazolam and single blood sampling to screen for effects of Pycnogenol(r) on the activity of the common drug metabolizing enzyme CYP3A4. For those subjects who are already receiving digoxin, we will use digoxin urine excretion to screen for effects of the botanical upon the activity of P-glycoprotein. Finally, we will continue the evaluation of a new questionnaire of lymphedema symptoms presently being tested as a tool for assessing the severity and improvement of symptoms with treatment. In summary, the successful completion of this research can be expected to provide an alternative therapy and new instruments for treating and measuring lymphedema.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphedema, Breast, Cancer
Keywords
lymphedema, breast, cancer, plant preparation, herbal preparation, pine bark extract

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
26 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Pycnogenol

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Unilateral (ipsilateral to breast cancer resection side) lymphedema of the upper extremity. Extravascular water ration of > 1.07/1 between affected vs. normal arm using multiple frequency bioelectric impedence Patient is > 2months from last surgical or radiation treatment to the affected axilla Renal and hepatic function: Creatinine clearance > 50ml/min, total bili <2 mg/dl, transaminases <1.5 x ULN Patient not pregnant or breastfeeding. Use of barrier contraception if sexually active. ECOG performance of 0-2 Patient not allergic to pycnogenol Exclusion criteria: Patients treated with their first course of chemotherapy or radiation Chemotherapy or radiation to axillary lymph node will exclude patients for 8 weeks following treatment Patients with more than one episode of arm cellulitis, venous clot, or woody fibrosis of the affected arm. Antibiotics used to treat cellulitis must be completed at least 4 weeks prior to initial screening Patients with a defibrillator Midazolam study only: Patients requiring or benefiting from supplemental oxygen, patients allergic to cherries
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James F. Cleary, M.B.B.S.
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Study Chair
Facility Information:
Facility Name
University of Wisconsin Comprehensive Cancer Center and School of Pharmacy
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53706
Country
United States

12. IPD Sharing Statement

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Pycnogenol for the Treatment of Lymphedema of the Arm in Breast Cancer Survivors

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