MR Imaging of the 3D Inguinal Hernia Scaffold ProFlor

NCT04762264 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2022-05-16

No results posted yet for this study

Summary

Demonstrating through MRI sequuences the regenerative features of the 3D inguinal hernia scaffold ProFlor

Conditions

  • Inguinal Hernia

Interventions

DEVICE

ProFlor inguinal hernia device

Device follow up after inguinal hernia repair with ProFlor

Sponsors & Collaborators

  • University of Cagliari

    lead OTHER

Principal Investigators

  • Giuseppe Amato · University of Cagliari

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2021-11-01
Completion
2021-12-01
FDA Device
Yes

Countries

  • Italy

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 NCT04762264 on ClinicalTrials.gov