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NCT04888624 · ClinicalTrials.gov registry record · NA

A Comparison Between Two Post-operative Dressings

A NA study, sponsored by SerenaGroup.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT04888624 is a NA study that has completed, run by SerenaGroup. The registered enrollment target is 20 participants.

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The verdict

NCT04888624, a NA study, has completed, sponsored by SerenaGroup.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

Surgical site infections are one of the leading causes of post-operative morbidity and mortality worldwide. The ideal post-operative dressing is impermeable and remains intact preventing contamination of the incision with microorganisms. In addition, it is often difficult for the patient to identify breaks in dressing integrity. This trial compares a post-operative dressing (DrySee® Inc. Houston Tx) with moisture detection allowing the patient to recognize when the dressing is compromised to a standard post-operative dressing (Tegaderm® + Pad, 3M, St. Paul, MN). The ideal dressing also allows the patient to shower without removing the dressing.

Interventions

  • DEVICE DrySee® dressing with moisture detection
  • DEVICE Tegaderm® + Pad transparent film dressing

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2021-09-13
Est. Completion 2022-02-01
Phase NA

Sponsor

SerenaGroup

10 total trials

What the Registry Record Tells You About NCT04888624

The ClinicalTrials.gov registry entry for NCT04888624 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SerenaGroup, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which DrySee® dressing with moisture detection is the first listed.

NCT04888624 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04888624 about?

NCT04888624 is a clinical study titled "A Comparison Between Two Post-operative Dressings". Surgical site infections are one of the leading causes of post-operative morbidity and mortality worldwide. The ideal post-operative dressing is impermeable and remains intact preventing contamination of the incision with microorganisms. In addition, it is often difficult for the patient to identify...

What is the current status of trial NCT04888624?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2021-09-13. Estimated completion is 2022-02-01.

What interventions are being tested in trial NCT04888624?

The interventions under investigation include: DrySee® dressing with moisture detection (DEVICE), Tegaderm® + Pad transparent film dressing (DEVICE).

Who is sponsoring clinical trial NCT04888624?

This trial is sponsored by SerenaGroup, which has 10 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.