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NCT02250183 · ClinicalTrials.gov registry record · NA

Medihoney and Santyl for Burn Injuries

A NA study, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

Terminated
Registry status
NA
Development phase
21
Enrollment target

NCT02250183: Clinical Trial NA study, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

NCT02250183 is a NA study that was terminated before completion, run by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute). The registered enrollment target is 21 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02250183, a NA study, was terminated before completion, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

TERMINATED
Registry status
NA
Development phase
21 participants
Enrollment target

Study Summary

This study is designed to assess the efficacy of MEDIHONEY® Gel with Active leptospermum honey dressing relative to SANTYL® ointment dressing on time to heal, bacterial growth in the wound, patient satisfaction, and treatment costs in patients with partial thickness burns. The study has four hypotheses: 1. It is hypothesized that MEDIHONEY® Gel with Active leptospermum honey will result in significantly faster wound healing (i.e., fewer days) when compared to SANTYL®. 2. It is hypothesized that MEDIHONEY® Gel with Active leptospermum honey sites will yield significantly fewer positive cultures for Pseudomonas aeruginosa and other bacteria when compared to SANTYL® sites. 3. It is hypothesized that patients will provide significantly higher patient care satisfaction ratings regarding their MEDIHONEY® Gel with Active leptospermum honey sites when compared to ratings with regard to their SANTYL® sites. 4. It is hypothesized that treatment costs, across participants, will be significantly lower for MEDIHONEY® Gel with Active leptospermum honey than for SANTYL®.

Primary Outcome

Pictures of wounds and associated "seepage test" paper towels, without indication of date or arm of treatment, were rated by two independent physicians regarding healed or not yet healed. This information was then be used to calculate a "time to heal" variable (# of days) for each patient.

Interventions

  • DEVICE MEDIHONEY® GEL WITH ACTIVE LEPTOSPERMUM HONEY
  • DEVICE Santyl

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2014-03-15
Est. Completion 2016-08-18
Phase NA

Why NCT02250183 stopped before completion

NCT02250183 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which MEDIHONEY® GEL WITH ACTIVE LEPTOSPERMUM HONEY is the first listed.

NCT02250183 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02250183 about?

NCT02250183 is a clinical study titled "Medihoney and Santyl for Burn Injuries". This study is designed to assess the efficacy of MEDIHONEY® Gel with Active leptospermum honey dressing relative to SANTYL® ointment dressing on time to heal, bacterial growth in the wound, patient satisfaction, and treatment costs in patients with partial thickness burns. The study has four hypothe...

What is the current status of trial NCT02250183?

This trial is currently terminated. It is a NA study. The enrollment target is 21 participants. The study started on 2014-03-15. Estimated completion is 2016-08-18.

What interventions are being tested in trial NCT02250183?

The interventions under investigation include: MEDIHONEY® GEL WITH ACTIVE LEPTOSPERMUM HONEY (DEVICE), Santyl (DEVICE).

Who is sponsoring clinical trial NCT02250183?

This trial is sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute), which has 34 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02250183's enrollment target sits among peer trials

21 1762nd of 2000 higher than 233 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 NCT02250183, the US trial registry maintained by the National Library of Medicine. NCT02250183 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.