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NCT01230489 · ClinicalTrials.gov registry record · NA

The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing

A NA study, sponsored by University of Missouri-Columbia.

Terminated
Registry status
NA
Development phase
13
Enrollment target

NCT01230489 is a NA study that was terminated before completion, run by University of Missouri-Columbia. The registered enrollment target is 13 participants.

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The verdict

NCT01230489, a NA study, was terminated before completion, sponsored by University of Missouri-Columbia.

TERMINATED
Registry status
NA
Development phase
13 participants
Enrollment target

Study Summary

To evaluate the efficacy of honey as a post surgical exit site care process to promote healing and prevent infectious bacterial colonization of newly created exit sites. It has been shown in the medical literature that honey has properties that are conducive to healing and the prevention of infection. In one study it was demonstrated that in urethral injury in the rat treated with honey the injury healed with none of the usual formation of fibrous tissue seen in such healing processes, that there was no reduction in the luminal diameter usually seen, and that the cells lining the urethra were uncompromised in any way, i.e. totally normal and healthy. We feel that if an exit site can be healed quickly with good normal tissue being developed that the patient will have a much better chance to keep that exit healthy reducing time, cost, and disruption of lifestyle. Other positive aspects of honey are it has the low pH required for good healthy tissue healing, it works in the presence of wound fluids, and it has never been shown to produce a resistant bacterial strain.

Interventions

  • BIOLOGICAL MediHoney

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2011-01
Est. Completion 2016-11-28
Phase NA

Sponsor

University of Missouri-Columbia

291 total trials

What the Registry Record Tells You About NCT01230489

The ClinicalTrials.gov registry entry for NCT01230489 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Missouri-Columbia, which has 291 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which MediHoney is the first listed.

NCT01230489 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01230489 about?

NCT01230489 is a clinical study titled "The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing". To evaluate the efficacy of honey as a post surgical exit site care process to promote healing and prevent infectious bacterial colonization of newly created exit sites. It has been shown in the medical literature that honey has properties that are conducive to healing and the prevention of infectio...

What is the current status of trial NCT01230489?

This trial is currently terminated. It is a NA study. The enrollment target is 13 participants. The study started on 2011-01. Estimated completion is 2016-11-28.

What interventions are being tested in trial NCT01230489?

The interventions under investigation include: MediHoney (BIOLOGICAL).

Who is sponsoring clinical trial NCT01230489?

This trial is sponsored by University of Missouri-Columbia, which has 291 total clinical trials registered on ClinicalTrials.gov.

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

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.