Clinical Trials Logo

Clinical Trial Summary

Quantitative radiographic imaging holds promise as a novel and innovative strategy to assess ventral hernia patients. Assessing abdominal wall changes surrounding ventral hernia using shear wave velocity values measured with ultrasound will identify features of the abdominal wall that differ between healthy volunteers and subjects scheduled to have ventral hernia repair. Through the use of ultrasound including shear wave velocity measurements, the abdominal wall of 25 subjects scheduled to have ventral hernia repair will be compared to those of 35 healthy volunteers. The ultrasound measurements will elucidate if ventral hernia affects abdominal wall elasticity and effect surgical outcomes.


Clinical Trial Description

ARFI-SWV Ultrasound holds promise as an inexpensive, noninvasive, point-of-care diagnostic tool for pre-operatively predicting successful hernia repair. The investigators propose to develop and refine a quantitative ultrasound protocol to measure abdominal wall features suitable for predicting successful closure of the midline fascia. ARFI-SWV ultrasound represents a novel and intriguing modality for real time visualization and characterization of changes in the biomechanical properties of diseased musculoskeletal tissues.

In this study, ARFI-SWV ultrasound is hypothesized to preoperatively measure the stiffness in the lateral abdominal wall as an estimation for mobility during hernia repair. Preoperatively evaluating hernia severity through ARFI-SWV ultrasound will be performed to identify mechanical characteristics of the abdominal musculature to predict success of midline fascial re-approximation in hernia patients. The study proposes to compare ultrasound images and associated shear wave velocity measurements between 35 healthy volunteers and 25 subjects undergoing surgical repair for ventral hernia. Subjects with ventral hernia will undergo imaging no earlier than two weeks prior to elective hernia repair and again postoperatively within six months following repair at a standard followup visit. Statistical analysis will determine if there is a significant difference in the abdominal wall stiffness, represented by the ultrasound shear wave velocity measurements, between the healthy subjects and the subjects with ventral hernia. Further analysis will determine if there is any statistically significant relationship between abdominal wall stiffness of subjects with ventral hernia and surgical outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03043079
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase N/A
Start date April 2016
Completion date September 15, 2017

See also
  Status Clinical Trial Phase
Terminated NCT03034213 - Gentrix™ Versus Biological or Prosthetic Mesh N/A
Enrolling by invitation NCT06306976 - Shear-Wave Elastography N/A
Not yet recruiting NCT06183840 - Only Mesh Fixation With Glue of Ventral/Incisional Laparoscopic Hernia Repair N/A
Completed NCT02206828 - The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Ventral Hernia Repair
Not yet recruiting NCT04624100 - Quality Control of Ventral Hernia Surgery by Prospective Registration
Active, not recruiting NCT03324854 - Use of Mosquito Net Mesh for Ventral Hernia Repair N/A
Not yet recruiting NCT05575141 - Robotic Versus Open Comparison in the Surgical Treatment of Wide Abdominal Wall Hernias N/A
Completed NCT01325792 - Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement N/A
Terminated NCT03317665 - Observational Biologic or Prosthetic Mesh
Recruiting NCT05576753 - Preperitoneal Umbilical Mesh Area N/A
Completed NCT05142761 - Tension in Posterior Component Separation for Abdominal Wall Reconstruction
Recruiting NCT03255239 - Open Preperitoneal Mesh Versus Retromuscular Mesh Versus Suture Repair for Abdominal Wall Hernias N/A
Completed NCT02129140 - Observational Study to Evaluate Ventral Incisional Hernia Repair Using a Biologic Mesh (Cook Biodesign)