Using a synthetic membrane to improve healing after tonsil surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of SupraTHEL 250, a synthetic biodegradable membrane, for mucosal reconstruction in the head and neck region following tonsillectomy. The membrane is applied to the surgical site to promote faster and less painful healing compared to traditional bare wound healing. The study aims to assess postoperative outcomes, including pain levels and healing rates, to determine if this approach enhances patient quality of life.

Why it matters

Who can join: the full rules

* 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.

Where it's running

• Vinzenz von Paul Kliniken gGmbH Marienhospital Stuttgart
  Stuttgart, Baden-Wurttemberg, Germany Recruiting

Study contacts

• Principal investigator: Alaa Emara — Cairo University
• Study coordinator: Alaa Emara
• Email: alaa.emara@polymedics.com
• Phone: +49711719500-182

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Ondansetron lozenge versus IV to prevent shivering after tonsil removal in children

  This test will see if an ondansetron lozenge works as well as intravenous ondansetron to prevent shivering in children aged 4 to 15 having a tonsillectomy.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.