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Long Term Function Outcomes and Pain in Implant-based Post-mastectomy Breast Reconstruction

NCT04477538 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2024-06-05

No results posted yet for this study

Summary

The objective of this proposal is to broadly assess patient physical functioning following breast reconstruction.

Conditions

  • Post-mastectomy Breast Reconstruction

Interventions

OTHER

Post-mastectomy breast reconstruction physical well-being survey

-The survey will ascertain: function status (BREAST Q - Physical Well Being Module and PROMIS upper extremity function), former interaction with physical or occupational therapy, amount of narcotics taken weekly due to chest/neck/breast pain, amount of Tylenol or similar anti-inflammatories taken weekly due to chest/neck/breast pain, and amount of muscle relaxants taken weekly due to chest/neck/breast pain.

Sponsors & Collaborators

  • Washington University School of Medicine

    lead OTHER

Principal Investigators

  • Terence Myckatyn, M.D. · Washington University School of Medicine

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-07
Primary Completion
2021-11-08
Completion
2021-11-08

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04477538 on ClinicalTrials.gov