Persistent Postmastectomy Pain: Defining the Burden of Disease and the Role of Surgical Reinnervation in Patients With Breast Reconstruction

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to find out how common persistent postmastectomy pain (PPMP) is among people who have had a mastectomy and breast reconstruction surgery for their breast cancer. The study will also look at how effective regenerative peripheral nerve interface (RPNI) surgery is for reducing pain from neuropathic PPMP after breast reconstruction.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

• Female

• Age ≥18 years

• History of mastectomy for breast cancer or genetic predisposition to breast cancer

• History of breast reconstruction with implants and/or autologous tissue

• At least 6 months of follow-up after reconstruction

• Patient treated at MSK

Locations
United States
New Jersey
Memoral Sloan Kettering Basking Ridge (Limited Protocol Activities)
RECRUITING
Basking Ridge
Memoral Sloan Kettering Monmouth (Limited protocol activities)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Suffolk-Commack (Limited protocol activity)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center (All protocol activites)
RECRUITING
New York
Memorial Sloan Kettering Nassau (Limited Protocol Activites)
RECRUITING
Rockville Centre
Contact Information
Primary
Danielle Rochlin, MD
rochlind@mskcc.org
646-608-8033
Backup
Babak Mahrara, MD
mehrarab@MSKCC.ORG
646-608-8085
Time Frame
Start Date: 2024-10-01
Estimated Completion Date: 2027-10-01
Participants
Target number of participants: 500
Treatments
Experimental: Postmastectomy Reconstruction Participants
Participants will be postmastectomy reconstruction and \>/= 6 months postoperative
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov