SUPRATHEL 250 as a Treatment for Oropharyngeal Wounds

Recruiting N/A Interventional Study
Tonsillitis Tonsillectomy Tonsillitis Recurrent
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
Alaa Emara · Other
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About This Trial

To assess the use of Suprathel 250 for mucosal reconstruction in oropharyngeal defects. The membrane will be applied after tonsillectomy procedures and compared to bare wounds' healing

Trial Locations
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Eligibility Criteria
* Indication for tonsillectomy according to the applicable clinical guideline. * Male or female patients aged 18 years or older. * Ability to understand the study information and provide written informed consent.
Contacts

Alaa Emara

+49711719500-182

alaa.emara@polymedics.com

CONTACT