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

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The Washington University

Status

Terminated

Conditions

Post-mastectomy Breast Reconstruction

Treatments

Other: Post-mastectomy breast reconstruction physical well-being survey

Study type

Observational

Funder types

Other

Identifiers

NCT04477538
202006199

Details and patient eligibility

About

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

Enrollment

240 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female
  • At least 18 years of age
  • Had a mastectomy for breast cancer or cancer prevention any time between 01/01/2010 and 06/30/2021.
  • Has undergone breast reconstruction surgery with plastic surgery faculty at the Washington University School of Medicine Division of Plastic and Reconstructive Surgery.
  • Able to understand and willing to sign an IRB-approved written informed consent document.

Exclusion criteria

-Known distant metastatic disease

Trial design

240 participants in 2 patient groups

Participants with prepectoral reconstruction
Description:
-Participants will complete the post-mastectomy breast reconstruction physical well-being survey
Treatment:
Other: Post-mastectomy breast reconstruction physical well-being survey
Participants with postpectoral reconstruction
Description:
-Participants will complete the post-mastectomy breast reconstruction physical well-being survey
Treatment:
Other: Post-mastectomy breast reconstruction physical well-being survey

Trial contacts and locations

1

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Central trial contact

Terence Myckatyn, M.D.

Data sourced from clinicaltrials.gov

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