RECRUITING

A Study on Pain After Breast Reconstruction

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-10-01
Study Completion:2027-10-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06627582

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Female
  2. * Age ≥18 years
  3. * History of mastectomy for breast cancer or genetic predisposition to breast cancer
  4. * History of breast reconstruction with implants and/or autologous tissue
  5. * At least 6 months of follow-up after reconstruction
  1. * Exchange or revision surgery within 6 months
  2. * Active medical reason for pain (e.g., infectious, neoplastic, wound related)
  3. * Greater than 15 years post-reconstruction

Contacts and Locations

Study Contact

Danielle Rochlin, MD
CONTACT
646-608-8033
rochlind@mskcc.org
Babak Mahrara, MD
CONTACT
646-608-8085
mehrarab@MSKCC.ORG

Principal Investigator

Danielle Rochlin, MD
PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center

Study Locations (Sites)

Memoral Sloan Kettering Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey, 07920
United States
Memoral Sloan Kettering Monmouth (Limited protocol activities)
Middletown, New Jersey, 07748
United States
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey, 07645
United States
Memorial Sloan Kettering Suffolk-Commack (Limited protocol activity)
Commack, New York, 11725
United States
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York, 10604
United States
Memorial Sloan Kettering Cancer Center (All protocol activites)
New York, New York, 10065
United States
Memorial Sloan Kettering Nassau (Limited Protocol Activites)
Rockville Centre, New York, 11553
United States

Collaborators and Investigators

Sponsor: Memorial Sloan Kettering Cancer Center

  • Danielle Rochlin, MD, PRINCIPAL_INVESTIGATOR, Memorial Sloan Kettering Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10-01
Study Completion Date2027-10-01

Study Record Updates

Study Start Date2024-10-01
Study Completion Date2027-10-01

Terms related to this study

Keywords Provided by Researchers

  • Postmastectomy Pain
  • breast reconstruction after mastectomy
  • breast reconstruction
  • mastectomy and breast reconstruction
  • mastectomy
  • mastectomy patient
  • 24-271
  • Memorial Sloan Kettering Cancer Center

Additional Relevant MeSH Terms

  • Mastectomy
  • Mastectomy Patient
  • Mastectomy and Breast Reconstruction
  • Breast Reconstruction
  • Breast Reconstruction After Mastectomy
  • Postmastectomy Pain