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NCT02992249 · ClinicalTrials.gov registry record

Prospective Evaluation of the ReCell® Autologous Cell Harvesting Device For Specific Compassionate Use Cases

A clinical trial, sponsored by Avita Medical.

Completed
Registry status
100
Enrollment target

NCT02992249 is a clinical trial that has completed, run by Avita Medical. The registered enrollment target is 100 participants.

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The verdict

NCT02992249 has completed, sponsored by Avita Medical.

COMPLETED
Registry status
100 participants
Enrollment target

Study Summary

This is a prospective uncontrolled observational study to evaluate clinical outcomes following use of the ReCell Autologous Cell Harvesting Device (ReCell) as an adjunct for closure (re-epithelialization) as a treatment of life-threatening wounds requiring grafting for closure, and associated skin graft donor sites, in patients who lack adequate available skin to harvest for conventional grafting. Treatment with the ReCell device may be performed as part of a single operative procedure, or multiple staged procedures as deemed clinically necessary. Adverse events associated with the use of the ReCell device/cell suspension will be documented. Subjects will be followed for 1 year following ReCell treatment.

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2014-05
Est. Completion 2020-06

Sponsor

Avita Medical

13 total trials

What the Registry Record Tells You About NCT02992249

The ClinicalTrials.gov registry entry for NCT02992249 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Avita Medical, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT02992249 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02992249 about?

NCT02992249 is a clinical study titled "Prospective Evaluation of the ReCell® Autologous Cell Harvesting Device For Specific Compassionate Use Cases". This is a prospective uncontrolled observational study to evaluate clinical outcomes following use of the ReCell Autologous Cell Harvesting Device (ReCell) as an adjunct for closure (re-epithelialization) as a treatment of life-threatening wounds requiring grafting for closure, and associated skin g...

What is the current status of trial NCT02992249?

This trial is currently completed. The enrollment target is 100 participants. The study started on 2014-05. Estimated completion is 2020-06.

Who is sponsoring clinical trial NCT02992249?

This trial is sponsored by Avita Medical, which has 13 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.