Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:07 AM
Ignite Modification Date:
2025-12-25 @ 4:07 AM
NCT ID:
NCT01153620
Eligibility Criteria:
Inclusion Criteria:
* Patients with acute traumatic cut, crush, abrasion, bite or stab wounds Provision of voluntary consent to participate in the study, following a full explanation of the nature and purpose of the study, by signing the informed consent form approved by the Institutional Ethics Committee (IEC) prior to all evaluations
* Wounds that are a minimum of approximately 4 cm2 in size
* Ability to read and understand the German patient information sheet and informed consent form
Exclusion Criteria:
* \< 18 years of age
* Pregnancy
* Immunosuppression
* Wounds caused by a burn
* Wounds that require treatment of hyaline cartilage, the central nervous system, peritoneum, meningae, inner / middle ear or inner eye
* Simultaneous participation in another clinical trial
* Wounds that require immediate surgical or medical treatment as well patients who are critically ill
* Patient with a known allergy to the active agent or any of the excipients
* Wounds that are \>3 cm in depth
* Wounds that have not received medical treatment for ≥6 hours
* Heavily bleeding wounds
* Open fractures, joints or tendons
* Wounds of the face
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01153620
Study Brief:
Protocol Section:
NCT01153620