search
Back to results

Mesh Suture for Internal Load Bearing Closures

Primary Purpose

Suture; Complications, Mechanical, Suture; Complications, Infection or Inflammation, Suture, Complication

Status
Active
Phase
Not Applicable
Locations
Armenia
Study Type
Interventional
Intervention
Duramesh Suturable Mesh
Sponsored by
Wigmore Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Suture; Complications, Mechanical focused on measuring suture, suture pull-through, suture sinus

Eligibility Criteria

1 Year - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Deep orthopedic soft tissue approximation

Exclusion Criteria:

  • Pregnancy
  • Age less than 1 year old
  • Repair of skin or other epithelial surfaces
  • Poor subcutaneous tissues
  • Ongoing infection

Sites / Locations

  • Wigmore Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Duramesh Suturable Mesh

Arm Description

Use of Duramesh Suturable Mesh for internal load bearing closures

Outcomes

Primary Outcome Measures

Surgery healing complication, acute
Number of patients with infection, drainage, seroma, wound disruption over the mesh suture closure

Secondary Outcome Measures

Surgery healing complication, delayed
Number of patients with infection, drainage, seroma, wound disruption, sinus over the mesh suture closure

Full Information

First Posted
April 28, 2019
Last Updated
September 27, 2022
Sponsor
Wigmore Clinic
search

1. Study Identification

Unique Protocol Identification Number
NCT03940560
Brief Title
Mesh Suture for Internal Load Bearing Closures
Official Title
Mesh Suture for Internal Load Bearing Closures
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2018 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wigmore Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Determine whether Mesh Suture achieves an acceptable safety and efficacy profile in load bearing internal tissue approximations. Mesh Suture has a novel design that permits tissue ingrowth and limits suture pull-through--items important for internal high-tension repairs
Detailed Description
Sutures are flexible linear elements that appose tissues and are "self-holding" with a surgically created knot. When tissues are under tension, such as the closure of an abdominal wall after laparotomy, the sutures cut through the tissues in what is known as "suture pull-through" and create incisional hernias. The hernia rate after primary laparotomy depends on the patient population, but is over 10%. In some high-risk populations, even with a small 3 cm laparoscopy incision, the hernia rate is over 30%. In primary hernia repair, use of sutures alone yields a 60% hernia recurrence rate at 10 years. Mesh has become commonplace in order to decrease incisional hernia recurrence rates in primary hernia repairs. A novel mesh suture, designed at Northwestern University (Chicago, IL) by Dr. Gregory Dumanian, has shown improved outcomes in pre-clinical animal models and these results are included at the end of this document. Dr. Dumanian has employed the concept of using a mesh-like suture already in his clinical practice. He has cut strips from an FDA-approved piece of hernia mesh, and used them as sutures, tying them with knots. Based on improved outcomes in pre-clinical and analogous clinical data in comparison to standard suture, Dr. Dumanian now proposes the use of a medical grade mesh suture of his design and fabrication in the load bearing internal tissue approximations. These are internal permanent sutures and will not be removed. They are made of the identical material (polypropylene) used in standard sutures. Mesh Sutures are larger than standard sutures and they automatically flatten to help resist suture pull-through. Tissue ingrowth around the filaments and into the suture improves their hold.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suture; Complications, Mechanical, Suture; Complications, Infection or Inflammation, Suture, Complication
Keywords
suture, suture pull-through, suture sinus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Safety and efficacy study
Masking
None (Open Label)
Allocation
N/A
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Duramesh Suturable Mesh
Arm Type
Experimental
Arm Description
Use of Duramesh Suturable Mesh for internal load bearing closures
Intervention Type
Device
Intervention Name(s)
Duramesh Suturable Mesh
Intervention Description
Use of Duramesh Suturable Mesh for internal load bearing closures
Primary Outcome Measure Information:
Title
Surgery healing complication, acute
Description
Number of patients with infection, drainage, seroma, wound disruption over the mesh suture closure
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Surgery healing complication, delayed
Description
Number of patients with infection, drainage, seroma, wound disruption, sinus over the mesh suture closure
Time Frame
Within 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Deep orthopedic soft tissue approximation Exclusion Criteria: Pregnancy Age less than 1 year old Repair of skin or other epithelial surfaces Poor subcutaneous tissues Ongoing infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Garen Koloyan, MD PhD
Organizational Affiliation
Wigmore Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wigmore Clinic
City
Yerevan
ZIP/Postal Code
0001
Country
Armenia

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Mesh Suture for Internal Load Bearing Closures

We'll reach out to this number within 24 hrs