CompletedNot Applicable

Celotres for Improvement in Wound Healing and Resulting Scar Consequences Following Suturing of a Wound

Poland, United Kingdom60 participantsStarted 2012-09

Plain-language summary

The objective of the study is to actively gather additional information on safety, device performance and possible emergent risks following the use of Celotres in a post-market setting when used to improve wound healing and the resulting scar consequences following suturing of a wound.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients electing to undergo a surgical procedure; * Patients able and willing to give written informed consent Exclusion Criteria: * Patients with a known or potential risk of allergy or sensitivity to products or substances containing porcine gelatin

What they're measuring

Safety

Timeframe: Assessed at treatment, suture removal, Months 1, 3, 6, 9 and 12

Trial details

NCT IDNCT01706848

SponsorHalscion, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2014-05

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