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A Multicenter, Prospective, Randomized Controlled Clinical Trial Assessing the Efficacy of a Novel Cellular, Acellular, Matrix-like Product (CAMP) Plus Standard of Care Versus Standard of Care Alone in the Management of Post-Mohs Micrographic Surgery Defects. (BIOMOHS)

6 de julio de 2026 actualizado por: BioLab Holdings
A multicenter, prospective, randomized controlled clinical trial assessing the efficacy of a novel cellular, acellular, matrix-like product (CAMP) plus standard of sare versus standard of sare slone in the management of post-mohs micrographic surgery defects.

Descripción general del estudio

Descripción detallada

This study will utilize a Prospective, Multicenter, Randomized Controlled Clinical Trial design.

Subjects will be adult patients undergoing Mohs micrographic surgery with resulting post-excisional defects suitable for healing by secondary intention or management with a topical matrix-like product.

Subjects will be randomized to receive:

  • CAMP plus Standard of Care (SOC), or
  • Control Dressing plus SOC. Randomization will occur after confirmation of final Mohs stage and measurement of the post-excisional defect.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

160

Fase

  • Fase 4

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • The potential subject must be at least 18 years of age or older.
  • The potential subject must have undergone Mohs micrographic surgery for a cutaneous malignancy (e.g., basal cell carcinoma, or squamous cell carcinoma).
  • The potential subject must have a post-Mohs surgical defect that is suitable for treatment with a CAMP product or healing by secondary intention.
  • The surgical site has received standard Mohs excision and hemostasis with no requirement for immediate flap or graft reconstruction as determined by the treating surgeon.
  • If the surgical defect is on the lower extremity, the limb must have adequate perfusion confirmed by vascular assessment. Any of the following methods performed within 3 months of the first screening visit are acceptable:

    1. Ankle-Brachial Index (ABI) between 0.7 and ≤ 1.3;
    2. Toe-Brachial Index (TBI) ≥ 0.6;
    3. Transcutaneous Oxygen Measurement (TCOM) ≥ 40 mmHg;
    4. Pulse Volume Recording (PVR): biphasic.
  • If the subject has multiple Mohs defects, they must be separated by at least 2 cm. The largest defect satisfying the inclusion and exclusion criteria will be designated as the target wound.
  • The potential subject must agree to attend the weekly study visits required by the protocol.
  • The potential subject must be willing and able to participate in the informed consent process.

Exclusion Criteria:

  • The potential subject is known to have a life expectancy of < 6 months.
  • The potential subject's target wound is not secondary to a Mohs excision. -

    -. The target wound is infected or there is cellulitis in the surrounding skin.

  • The target wound:

    1. Exposes tendon, bone, or joint space, and/or[MM6.1][RB6.2]
    2. Requires immediate complex flap or graft reconstruction in the judgment of the surgeon.
  • The potential subject has participated in a clinical trial involving treatment with an investigational product within the previous 30 days.
  • The potential subject has glycated hemoglobin (HbA1c) greater than 10% within 3 months of the initial screening visit.
  • The potential subject, in the opinion of the investigator, has a medical or psychological condition that may interfere with study assessments.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: Control Dressing + Standard of Care
Standard of care will be cleaning, debridement, ulcer moisture balance, control dressing and offloading.
Beginning at the screening visit, participants will receive weekly treatment with standard of care (cleaning, debridement, ulcer moisture balance, and offloading) until ulcer closure, or a maximum of 6 weeks, whichever occurs first.
Otro: CAMP + Standard of Care
Membrane Wrap-Lite is a human amniotic membrane tissue allograft derived from human placental tissue.
Participants will receive weekly applications of caregraFT™ and Standard of Care until ulcer closure, or a maximum of 6 weeks, whichever occurs first.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Complete Wound Closure
Periodo de tiempo: 1-6 Weeks
The percentage of target wounds achieving complete wound closure in 6 weeks.
1-6 Weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Time to Closure
Periodo de tiempo: 1-6 Weeks
Time to closure for the target wound.
1-6 Weeks
Percentage Area Reduction
Periodo de tiempo: 1-6 weeks
Percentage wound area reduction from TV-1 to TV-6 measured weekly with digital photographic planimetry using imaging device and physical examination.
1-6 weeks
Procedure-Related Adverse Events
Periodo de tiempo: 1-6 Weeks
The number of product- or procedure-related adverse events.
1-6 Weeks
Wound Volume Reduction
Periodo de tiempo: 1-6 Weeks
Percentage wound volume reduction from TV-1 to TV-6 measured weekly with digital photographic planimetry using imaging device and physical examination.
1-6 Weeks
Product or Procedure Adverse Events
Periodo de tiempo: 1-6 Weeks
The number of product- or procedure-related adverse events.
1-6 Weeks
Numeric Pain Scale
Periodo de tiempo: 1-6 weeks
Change in pain at the target wound site assessed using a numeric pain scale. 0 being no pain and 10 being the worst pain imaginable.
1-6 weeks
Economic Outcomes
Periodo de tiempo: 1-6 Weeks
Health economic outcomes, including direct and indirect cost of care.
1-6 Weeks
Quality of Life
Periodo de tiempo: 1- 6 Weeks
Change in quality of life, using the Wound Quality of Life questionnaire. [Time frame: TV-1, TV-4, TV-6/final visit].
1- 6 Weeks
Scare and Cosmetic Outcomes
Periodo de tiempo: 12 Months
Scar and cosmetic outcomes at 12 months using the Patient and Observer Scar Assessment Scale (POSAS). 0 being normal and 10 being very different.
12 Months
Time to Complete Granulation Tissue
Periodo de tiempo: 1-6 Weeks
Time to complete granulation tissue confirmed by independent assessment.
1-6 Weeks

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Perfusion
Periodo de tiempo: 1-6 Weeks
1. Changes in local perfusion at the surgical site over the 6-week treatment period, assessed via near-infrared spectroscopy.
1-6 Weeks
Rate of Recurrence
Periodo de tiempo: 12 Months
The rate of recurrence within 12 months of closure when applicable.
12 Months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Thomas Serena, MD, Serena Group, Inc.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de julio de 2026

Finalización primaria (Estimado)

1 de julio de 2028

Finalización del estudio (Estimado)

1 de julio de 2028

Fechas de registro del estudio

Enviado por primera vez

6 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de julio de 2026

Publicado por primera vez (Actual)

10 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

6 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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