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The Use of Cryotherapy to Prevent Paclitaxel-induced Peripheral Neuropathy and Nail Changes in Women With Breast Cancer

Primary Purpose

Cryotherapy Effect, Peripheral Neuropathy, Nail Toxicity

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
cryotherapy
Sponsored by
Parkview Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cryotherapy Effect

Eligibility Criteria

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

Inclusion Criteria:

  • Females 18 or older
  • Histologically confirmed diagnosis of breast cancer
  • Receiving neo-adjuvant or adjuvant dose-dense anthracycline (AC) plus taxane-based chemotherapy or paclitaxel in combination with trastuzumab and pertuzumab

Exclusion Criteria:

  • Prior taxane therapy
  • Prior oxaliplatin therapy
  • Non-English speaking
  • History of peripheral neuropathy, i.e., Buerger's disease
  • History of diabetes mellitus
  • Pre-existing peripheral neuropathy from other conditions, e.g., Raynaud's disease, Guillain-Barre, Miller Fisher Syndrome
  • Hand, nail or foot conditions, e.g., hand/foot syndrome, arthritis, hammer toe, carpal tunnel, bunions, deformities
  • Alcohol abuse (history/current)
  • Current medication usage of opioids, anti-depressants, anti-convulsants, glutamines, vitamin B12

Sites / Locations

  • Parkview Cancer Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Interventioncryotherapy/control

standard of care

Arm Description

Subjects will have one mitt/one slipper and serve as their own control

Subjects will have two mitts/slippers

Outcomes

Primary Outcome Measures

Numbness,tingling,pain ,nail toxicities
absence of numbness and tingling in the treated hands/feet If there is an absence of pain in the treated hands/feet If there is an absence of nail changes in the treated hands/feet

Secondary Outcome Measures

Full Information

First Posted
September 3, 2020
Last Updated
March 4, 2021
Sponsor
Parkview Health
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1. Study Identification

Unique Protocol Identification Number
NCT04558034
Brief Title
The Use of Cryotherapy to Prevent Paclitaxel-induced Peripheral Neuropathy and Nail Changes in Women With Breast Cancer
Official Title
The Use of Cryotherapy to Prevent Paclitaxel-induced Peripheral Neuropathy and Nail Changes in Women With Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
Principal Investigator retired before study completed.
Study Start Date
August 4, 2020 (Actual)
Primary Completion Date
February 3, 2021 (Actual)
Study Completion Date
February 3, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Parkview Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will determine the efficacy of cryotherapy to prevent paclitaxel-induced peripheral neuropathy and nail changes in women with breast cancer.
Detailed Description
Women with breast cancer receiving paclitaxel will complete the Brief Pain Inventory(BPI), Neuropathic Pain Syndrome Inventory (NPSI)while a member of the research team will conduct an assessment of their nails. Once complete, cryotherapy will be administered 15 minutes prior to the paclitaxel infusion, continuously during and then 15 minutes after completion of the paclitaxel for a total of 90 minutes. Cyrotherapy will be delivered using Elasto-gel mitts and Rapid relief slippers. These items will be changed 45min after initiation to ensure coldness. There will be two arms of the study. One arm will include subjects who will wear one slipper/one mitt on their foot/hand while the other foot/hand will serve as a control. The other arm will include subjects who will have cryotherapy to both hands and feet. . This process will be repeated for a total of 12 times in conjunction with 12 doses of paclitaxel. At time point 13, during a routine visit to their oncologist, the subjects nails will be reassessed along with completion of the BPI and NPSIA total of 25 subjects will be enrolled in each arm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cryotherapy Effect, Peripheral Neuropathy, Nail Toxicity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
There are 2 arms to the study.The Elasto-gel mitt and Rapid Relief slipper will be placed either on one hand/foot or both based on the patient's medical oncologist. All subjects will have a standardized onset/duration of therapy which includes the following : 15 minutes prior to the paclitaxel infusion, Continuously during the paclitaxel infusion, 15 minutes after completion of paclitaxel for a total of 90 minutes.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Interventioncryotherapy/control
Arm Type
Active Comparator
Arm Description
Subjects will have one mitt/one slipper and serve as their own control
Arm Title
standard of care
Arm Type
No Intervention
Arm Description
Subjects will have two mitts/slippers
Intervention Type
Other
Intervention Name(s)
cryotherapy
Intervention Description
cryotherapy will be delivered
Primary Outcome Measure Information:
Title
Numbness,tingling,pain ,nail toxicities
Description
absence of numbness and tingling in the treated hands/feet If there is an absence of pain in the treated hands/feet If there is an absence of nail changes in the treated hands/feet
Time Frame
13 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Females 18 or older Histologically confirmed diagnosis of breast cancer Receiving neo-adjuvant or adjuvant dose-dense anthracycline (AC) plus taxane-based chemotherapy or paclitaxel in combination with trastuzumab and pertuzumab Exclusion Criteria: Prior taxane therapy Prior oxaliplatin therapy Non-English speaking History of peripheral neuropathy, i.e., Buerger's disease History of diabetes mellitus Pre-existing peripheral neuropathy from other conditions, e.g., Raynaud's disease, Guillain-Barre, Miller Fisher Syndrome Hand, nail or foot conditions, e.g., hand/foot syndrome, arthritis, hammer toe, carpal tunnel, bunions, deformities Alcohol abuse (history/current) Current medication usage of opioids, anti-depressants, anti-convulsants, glutamines, vitamin B12
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danielle R Payne, MSN
Organizational Affiliation
Parkview Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parkview Cancer Institute
City
Fort Wayne
State/Province
Indiana
ZIP/Postal Code
46845
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The following will be shared: Individual participant data that underlie the results reported in the planned article after deidentification including text,tables,figures, appendices
IPD Sharing Time Frame
Immediately following publication and no end date
IPD Sharing Access Criteria
Data will be available to anyone who wishes to access the data for any purpose by contacting nancy.ehmke@parkview.com
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The Use of Cryotherapy to Prevent Paclitaxel-induced Peripheral Neuropathy and Nail Changes in Women With Breast Cancer

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