Ventral Hernia Clinical Trial
Official title:
Prospective Measurements of Intra-Abdominal Volume and Pulmonary Function After Repair of Massive Ventral Hernias With the Components Separation Technique
Verified date | May 2009 |
Source | Northwestern University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
Immediate post-operative abdominal compartment syndrome is a feared complication after hernia repair in patients with a "loss of abdominal domain." Replacement of the viscera within an unyielding stiff abdominal wall may compromise the perfusion of the intestines, elevate the diaphragm, and interfere with ventilation. The components separation technique, used to repair these massive hernias, employs bilateral relaxing incisions in the external oblique muscle and fascia in order to approximate the rectus abdominis muscles in the midline. Reducing a large volume hernia into the abdominal cavity and primary closure of the abdominal wall should cause problems both with abdominal compartment pressure and with postoperative ventilation, but in the investigators' 13-year experience with over 250 cases, this has not been seen clinically, and the investigators sought to understand why. The investigators' hypothesis is that releasing the rectus muscles from the external obliques expands the intra-abdominal compartment, reclaims lost domain, and thus reduces abdominal pressure and respiratory problems. The investigators have previously reported increased abdominal volumes using the components separation technique in a retrospective series, but patients were not standardized for the collection of data, and no pulmonary function tests were obtained in that series (Hadad, in press). The purpose of this study was to prospectively analyze the effect of this surgical technique on abdominal volume and pulmonary function.
Status | Completed |
Enrollment | 21 |
Est. completion date | December 2008 |
Est. primary completion date | December 2008 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - any patient with a large ventral hernia already scheduled to undergo ventral hernia repair with components separation technique Exclusion Criteria: - any patient unwilling to comply with pre-operative pulmonary function testing, or postoperative pulmonary function testing or postoperative one-time abdominal CT scan |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Division of Plastic and Reconstructive Surgery, Northwestern.edu | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Northwestern University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in abdominal volume | 3 months following hernia repair | No | |
Secondary | Change in pulmonary function | 3 months following hernia repair | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06016426 -
Mass Closure vs Layer by Layer Closure
|
N/A | |
Recruiting |
NCT05572021 -
A Comparison of the Outcomes in Fortiva and Strattice Mesh
|
N/A | |
Completed |
NCT02292264 -
Risk Factors and Complications of Ventral Hernia Repair
|
||
Completed |
NCT02263599 -
Conservative Treatment For Ventral Hernia
|
||
Completed |
NCT02263625 -
Regional Differences In Indication for Ventral Hernia Repair
|
||
Completed |
NCT01961687 -
A Prospective, Multi-Center Study of Phasix™ Mesh for Ventral or Incisional Hernia Repair.
|
N/A | |
Completed |
NCT01325246 -
Reoperation Rate Versus Clinical Recurrence After Ventral Hernia Repair
|
N/A | |
Completed |
NCT03283982 -
Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM
|
N/A | |
Not yet recruiting |
NCT05526209 -
Longitudinal Relaxing Incision as a Technique for Recurrence Prevention in Ventral Hernia
|
||
Completed |
NCT04438369 -
Evaluation of Ultrasound-guided Erector Spinae Block for Postoperative Analgesia in Laprascopic Ventral Hernia Repair.
|
N/A | |
Recruiting |
NCT04173884 -
Video-based Collaborative Learning to Improve Ventral Hernia Repair
|
N/A | |
Recruiting |
NCT02703662 -
Performance of Biologic Mesh Materials in Abdominal Wall Reconstruction
|
Phase 2/Phase 3 | |
Completed |
NCT03938688 -
Randomized Control Trial Comparing Transfascial Suture for Mesh Fixation to No Mesh Fixation
|
N/A | |
Completed |
NCT01719718 -
The Influence of Closing the Gap on Postoperative Seroma and Recurrences in Laparoscopic Ventral Hernia Repair
|
N/A | |
Completed |
NCT03342040 -
Transverse Abdominis Plane Block in Laparoscopic Ventral Hernia Repair
|
N/A | |
Completed |
NCT04150796 -
Comparing eTEP and Laparoscopic Intraperitoneal Onlay Mesh (IPOM) for Ventral Hernias
|
N/A | |
Recruiting |
NCT03222102 -
Ventral Hernia Prevention After Liver Transplantation
|
N/A | |
Completed |
NCT05610267 -
Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair
|
||
Terminated |
NCT01794338 -
The Use of Biologic Mesh vs Bioabsorbable Mesh During Ventral Hernia Repair in At-risk Patients
|
N/A | |
Completed |
NCT01886963 -
A Clinical Trial Using Spy Elite System in Planning Tissue Advancement Flaps After Ventral Hernia Repair
|
N/A |