Comparison of Sample Characteristics Between Subjects Who Received Strattice Mesh for Abdominal Wall Reconstruction
NCT ID: NCT04534920
Last Updated: 2021-09-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
182 participants
OBSERVATIONAL
2020-07-27
2021-12-13
Brief Summary
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Detailed Description
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Study Design Two different datasets from Institutional Review Board (IRB) approved studies L#12,083 and L#12,086 will be used to compare the sample characteristics between subjects who received Strattice mesh for abdominal wall reconstruction at Westchester Medical Center and Americas Hernia Society Quality Collaborative (AHSQC) registry.
Primary Objective: To determine the degree to which our sample of StratticeĀ® recipients resemble AHSQC StratticeĀ® recipients.
Study Summary:
This study involves two different datasets from our existing studies L#12083 and L#12,086 which are approved by New York Medical College, IRB on 6/14/2017and 7/7/2017 respectively.
Study L#12,083 is a retrospective data collection of subjects who had abdominal wall reconstruction and received Strattice mesh during 1/1/2011 to 12/31/2018 at Westchester Medical Center. A total of 105 records from this study will be used for comparison study. Study L#12086 is a prospective study of subjects who had abdominal wall reconstruction using biological mesh. A total of 77 records will be used from this study. From both the studies combined we have about a total of 182 records of extracted data and same data variables will be used to compare with AHSQC registry. The data that will be compared includes preoperative info, hospital course, complications, re-hospitalizations and 2weeks follow-up.
Research Subject Population:
Number of Subjects Total of 182 records met the inclusion criteria and data has been collected.
Gender of Subjects There will be no gender based restrictions for this study.
Age of Subjects Subjects 18 to 85 years old will be included in this study.
Conditions
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Study Design
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OTHER
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Subjects who had complex abdominal wall reconstruction and received biologic mesh are included in the study
Exclusion Criteria
* Any hernia repair not using biologic mesh are excluded.
18 Years
85 Years
ALL
No
Sponsors
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New York Medical College
OTHER
Responsible Party
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Rifat Latifi
The Felicien Steichen Professor and Chairman of Surgery
Principal Investigators
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Rifat Latifi, MD
Role: PRINCIPAL_INVESTIGATOR
Chairman Department of Surgery
Locations
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Westchester Medical center
Valhalla, New York, United States
Countries
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Other Identifiers
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14073
Identifier Type: -
Identifier Source: org_study_id
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