Randomized Double-Blind Controlled Clinical Trial

Completed · Not applicable

Conditions studied: Chronic Wounds, Acute Wounds

In brief

The study is a randomized double-blind controlled clinical trial designed to compare the ability of NaOCl to NSS in the reduction of bacterial burden in nonhealing acute and chronic wounds.

Key facts

Study ID

NCT04320628

Run by

SerenaGroup, Inc.

People needed

25

Starts

2020-05-20

Expected to finish

2022-03-01

Last updated by the study team

2022-03-14

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients with acute or chronic wounds that have been present for a minimum of 4 weeks.
• A signed and dated informed consent form.
• Subject is willing and able to comply with instructions and scheduled visits.

You may not qualify if…

• The Subject has other concurrent conditions that in the opinion of the Investigator may compromise subject safety.
• The subject's wound has not been present for at least 4 weeks.

Where it is running

• Serena Group Research Institute — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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