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NCT04906408 · ClinicalTrials.gov registry record · NA

The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR

A NA study of Abdomen Hernia, sponsored by Ohio State University.

Recruiting
Registry status
NA
Development phase
300
Enrollment target
1
Study location

NCT04906408: Recruiting NA study of Abdomen Hernia, sponsored by Ohio State University.

NCT04906408 is a NA study of Abdomen Hernia that is actively recruiting participants, run by Ohio State University. The registered enrollment target is 300 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04906408, a NA study of Abdomen Hernia, is actively recruiting participants, sponsored by Ohio State University.

RECRUITING
Registry status
NA
Development phase
300 participants
Enrollment target
1
Study location

Study Summary

Randomized controlled trial to compare SSO's in abdominal wall reconstruction patients using Prevena, Prineo, and traditional incisional dressings.

Conditions Studied

Interventions

  • DEVICE Prevena
  • DEVICE Prineo
  • DRUG Traditional

Study Locations (1)

Ohio

  • Department of Plastic Surgery - Columbus

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2021-09-17
Est. Completion 2028-05-01
Phase NA
Ohio State University

552 total trials

What NCT04906408 shows while recruiting

NCT04906408 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower).

The record links to 1 condition, with Abdomen Hernia appearing as the primary indexed condition, and to 3 interventions - of which Prevena is the first listed.

NCT04906408 reports a single indexed study location in Ohio.

Frequently Asked Questions

What is clinical trial NCT04906408 about?

NCT04906408 is a clinical study titled "The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR". Randomized controlled trial to compare SSO's in abdominal wall reconstruction patients using Prevena, Prineo, and traditional incisional dressings.

What is the current status of trial NCT04906408?

This trial is currently recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2021-09-17. Estimated completion is 2028-05-01.

What conditions does trial NCT04906408 study?

This clinical trial studies the following conditions: Abdomen Hernia.

What interventions are being tested in trial NCT04906408?

The interventions under investigation include: Prevena (DEVICE), Prineo (DEVICE), Traditional (DRUG).

Who is sponsoring clinical trial NCT04906408?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04906408 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT04906408's enrollment target sits among peer trials

300 330th of 2000 higher than 1,630 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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Source: ClinicalTrials.gov NCT04906408, the US trial registry maintained by the National Library of Medicine. NCT04906408 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.