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NCT03283982 · ClinicalTrials.gov registry record · NA
Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 75
- Enrollment target
NCT03283982: Completed NA study, sponsored by The Cleveland Clinic.
NCT03283982 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 75 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03283982, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 75 participants
- Enrollment target
Study Summary
The investigators aim to conduct a registry-based, randomized controlled trial to investigate if the robotic platform for minimally invasive ventral hernia repair with intraperitoneal onlay mesh (IPOM), when compared to the laparoscopic platform, will influence on early postoperative pain scores, wound morbidity (surgical site infections, surgical site occurrences and surgical site occurrences requiring procedural intervention), ventral hernia recurrence rate and abdominal wall-specific quality of life.
Primary Outcome
Pain scores will be assessed using the Numeric Pain Rating Scale (NRS-11); The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable"); This will be reported using median and interquartile ranges
Interventions
- DEVICE Robotic Ventral Hernia Repair with IPOM
- DEVICE Laparoscopic Ventral Hernia Repair with IPOM
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2017-09-11 |
| Est. Completion | 2021-01-31 |
| Phase | NA |
What the finished NCT03283982 record still lists
NCT03283982 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which Robotic Ventral Hernia Repair with IPOM is the first listed.
NCT03283982 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03283982 about?
NCT03283982 is a clinical study titled "Laparoscopic vs. Robotic Ventral Hernia Repair With IPOM". The investigators aim to conduct a registry-based, randomized controlled trial to investigate if the robotic platform for minimally invasive ventral hernia repair with intraperitoneal onlay mesh (IPOM), when compared to the laparoscopic platform, will influence on early postoperative pain scores, wo...
What is the current status of trial NCT03283982?
This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2017-09-11. Estimated completion is 2021-01-31.
What interventions are being tested in trial NCT03283982?
The interventions under investigation include: Robotic Ventral Hernia Repair with IPOM (DEVICE), Laparoscopic Ventral Hernia Repair with IPOM (DEVICE).
Who is sponsoring clinical trial NCT03283982?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03283982's enrollment target sits among peer trials
75 1069th of 2000 higher than 919 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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