Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT03082391 · ClinicalTrials.gov registry record · NA
Heavy Weight Versus Medium Weight Mesh in Ventral Hernia Repair
A NA study of Ventral Hernia, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 350
- Enrollment target
- 1
- Study location
NCT03082391 is a NA study of Ventral Hernia that has completed, run by The Cleveland Clinic. The registered enrollment target is 350 participants, above the 123-participant average among 18 other Ventral Hernia trials with a reported enrollment target (185% higher). The trial reports 1 study location across 1 state.
The verdict
NCT03082391, a NA study of Ventral Hernia, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 350 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine if mesh weight has an impact on postoperative pain, ventral hernia recurrence, incidence of deep wound infection, and overall quality of life following ventral hernia repair with mesh.
Conditions Studied
Interventions
- DEVICE Heavy weight Mesh
- DEVICE Medium weight Mesh
Study Locations (1)
Ohio
- Cleveland Clinic Foundation - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 350 participants |
| Start Date | 2017-03-14 |
| Est. Completion | 2020-05-28 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03082391
The ClinicalTrials.gov registry entry for NCT03082391 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 123-participant average among 18 other Ventral Hernia trials with a reported enrollment target (185% higher). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Ventral Hernia appearing as the primary indexed condition, and to 2 interventions - of which Heavy weight Mesh is the first listed.
NCT03082391 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT03082391 about?
NCT03082391 is a clinical study titled "Heavy Weight Versus Medium Weight Mesh in Ventral Hernia Repair". The purpose of this study is to determine if mesh weight has an impact on postoperative pain, ventral hernia recurrence, incidence of deep wound infection, and overall quality of life following ventral hernia repair with mesh.
What is the current status of trial NCT03082391?
This trial is currently completed. It is a NA study. The enrollment target is 350 participants. The study started on 2017-03-14. Estimated completion is 2020-05-28.
What conditions does trial NCT03082391 study?
This clinical trial studies the following conditions: Ventral Hernia.
What interventions are being tested in trial NCT03082391?
The interventions under investigation include: Heavy weight Mesh (DEVICE), Medium weight Mesh (DEVICE).
Who is sponsoring clinical trial NCT03082391?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03082391 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Ventral Hernia
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
AFFIX: Post-market Study of MaxTack™ Motorized Fixation Device in Subjects Undergoing Ventral Hernia Repair
RECRUITING · NA
-
Robotic Versus Open Ventral Hernia Repair
RECRUITING · NA
-
Clinical Investigation of the da Vinci Surgical System
ACTIVE NOT RECRUITING · NA
-
Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable Hernia Repair)
ACTIVE NOT RECRUITING · NA
-
Pilot Trial of Abdominal Core Rehabilitation To Improve Outcomes After Ventral Hernia Repair
ACTIVE NOT RECRUITING · NA
-
CYP2D6 Genotype-guided Management of Opioid Analgesics in Patients Undergoing Elective Ventral Hernia Repairs
ACTIVE NOT RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.