Myriad™ Augmented Soft Tissue Reconstruction Registry
Recruiting
Observational Study
Abdominal Wound Dehiscence
Necrotizing Soft Tissue Infection
Lower Extremity Wound
Pilonidal Sinus
Anal Fistula
Hidradenitis Suppurativa
Pressure Injury
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 800 (estimated)
- Sponsor
- Aroa Biosurgery Limited · Industry
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About This Trial
This is an observational study designed to evaluate the safety and clinical outcomes of Myriad™ in soft tissue reconstruction procedures. The study will enroll participants who are undergoing a surgical procedure, where the attending physician will use Myriad™ as part of the surgical intervention.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Willing and able to provide written informed consent and to comply with the requirements of Clinical Investigational Plan
* Male or female patients aged 18 years or above
* Patients where Matrix and/or Morcells were used as part of their soft tissue reconstruction procedure
* …
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