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Post Market Clinical Follow Up to "Patient Reported Outcome" Using a Titanised Polypropylene Mesh (TiLOOP® Bra Pocket)

NCT03868514 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 313

Last updated 2023-11-18

No results posted yet for this study

Summary

"PRO-Pocket" - International prospective multicentre Post Market Clinical Follow Up to "Patient reported outcome" in primary or secondary breast reconstruction after mastectomy using a titanised polypropylene mesh (TiLOOP® Bra Pocket)

Conditions

  • Breast Reconstruction After Mastectomy
  • Breast Neoplasm
  • Breast Cancer
  • Breast Diseases

Interventions

DEVICE

TiLOOP® Bra Pocket

Primary or secondary breast reconstruction following mastectomy with titanised polypropylene mesh TiLOOP® Bra Pocket

Sponsors & Collaborators

  • pfm medical gmbh

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-07-04
Primary Completion
2022-06-22
Completion
2023-11-15

Countries

  • Austria
  • Germany

Study Locations

More Related Trials

Entities

Diseases

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 NCT03868514 on ClinicalTrials.gov