ClinicalTrials.Veeva

Menu

The Impact of Abdominal Wall Reconstruction on Abdominal Wall Tension and Intra-Abdominal Pressure

NeuroTherapia, Inc. logo

NeuroTherapia, Inc.

Status

Terminated

Conditions

Incisional Hernia
Ventral Hernia
Parastomal Hernia

Treatments

Device: Abdominal wall tension
Device: Intra-abdominal pressure

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a prospective cohort study. Patients have an incisional or parastomal hernia with >20 cm fascial defect on pre-operative imaging who will undergo an anticipated open bilateral transversus abdominis release with retromuscular synthetic mesh will have their abdominal wall tension measured using a tension scale and their intra-abdominal pressure measured using a urinary catheter containing pressure sensors. The investigators aim to quantify the changes, as well as explore and describe the physiologic shifts that may be associated with these changes.

Enrollment

2 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients ≥ 18 years of age
  • Incisional or parastomal hernia with >20 cm fascial defect on pre-operative imaging
  • Anticipated open bilateral transversus abdominis release with retro-muscular synthetic mesh placement

Exclusion criteria

  • Pregnant patients
  • Require a Legally Authorized Representative (LAR) to sign the informed consent form

Trial contacts and locations

1

Loading...

Central trial contact

Benjamin T Miller, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems