Study to Evaluate the Effectivity and Safety of BIOSCAFF®H Compared to DuraGen®, in Patients Undergoing Dural Repair

Top Health S.A.P.I DE C.V.

Status: Terminated

Conditions: Cerebrospinal Fluid Leakage

Treatments: Device: Bovine collagen matrix graft; Device: Human collagen matrix graft

Study type: Observational

Funder types: Industry; Other

Identifiers

NCT06419855

TOP-1122-IV

Details and patient eligibility

About

Study in which the presence or absence of symptoms or any health condition is observed and recorded 30 days after a cranial surgery in which the physician places a material or graft, either BIOSCAFF®H or DuraGen®, into the skull; this material allows the regeneration of tissue that makes up one of the layers of the brain that was affected before or during surgery. The primary hypothesis of this study is that there will be no more than a 10% difference in outcomes between the BIOSCAFF®H device and the active comparator, DuraGen®, with respect to the incidence of cerebrospinal fluid leak or the presence of pseudomeningocele.

Full description

This study will help describe the safety profile and other aspects such as quality of life of the subjects who received it. The primary objective of the study is to evaluate the efficacy of the BIOSCAFF® H graft in patients undergoing dural surgery in the absence of cerebrospinal fluid leakage compared to the active comparator.

This is a prospective, multicenter, cohort, post-approval study to evaluate the efficacy and safety of BIOSCAFF®H. It consists of a screening period and a follow-up period up to 52 weeks after surgery. Medical records of patients who underwent surgery less than 30 days post-operatively and were implanted with the BIOSCAFF®H human collagen dural substitute or the active bovine collagen-based comparator, DuraGen®, will be considered. It is estimated that approximately 86 dural surgery patients will be enrolled.

Enrollment: 2 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adults ≥18 years of age up to 70 years of age, of both sexes.
• Patients who agree to participate and are able to provide written informed consent.
• Patients who underwent dural surgery or duraplasty for pathological processes or who required dural grafting at the neurosurgeon's discretion with a maximum of 30 days postoperatively.
• Patients in need of an incision of at least 2 cm in length.

Exclusion criteria

• Presence of empyema/subdural abscess or any type of systemic infection affecting/infiltrating the dura mater detected by the physician prior to surgery.

• Diagnosis of malignant cranial tumor(NOTE: patients without a diagnosis of malignancy will still be allowed to enter the study).

  • The diagnosis of malignancy will be considered according to the classification of Tumors of the Central Nervous System, stipulated by the World Health Organization version 2021, considering the lowest taxonomic hierarchy (specific) of the tumor available in the diagnosis considering: Category, family or class, type and subtype.
  • The ICD-O morphological coding system will be used, to classify tumors as benign (Eligible) and malignant (Ineligible), considering: /0 for benign tumors; /1 nonspecific, borderline or of uncertain behavior as tumors that can be included in the study, while those coded as /2, /3 and /6 or metastatic tumors as ineligible. In APPENDIX 4 "Patient eligibility associated with the listing of tumors in the central nervous system" the classification of tumors according to the above-mentioned document is listed for clearer reference.

• Drowsy or comatose patients at the time of screening.

• Serum creatinine levels >2.0 mg/dL.

• Patient with a total bilirubin level >2.5 mg/dL.

• Previous surgery at the same site or patients with a previous craniotomy/craniectomy within 6 months prior to the study surgery.

• Inability to read and understand protocol information by the participant.

• History of symptomatic hydrocephalus.

• Patients who have received chemotherapy or radiation therapy in the surgical region that was completed within 3 months prior to the planned surgery or are scheduled for the next 12 weeks.

• Known history of hemophilia or other clinically significant coagulopathy.

• Previous participation in any related device or investigational drug study within 30 days prior to screening.

• Medical history report of status epilepticus in the patient.

• Patients with uncontrolled diabetes according to ADA criteria: fasting glucose ≥200 mg/dL, HbA1C ≥8.5%.

• Patients in whom radiological contrast medium is contraindicated.

• Women who are breastfeeding or pregnant.

• Patients with a body mass index (BMI) ≥ 35 kg/m2.

Trial design

2 participants in 2 patient groups

Human collagen matrix graft

Description:

Is a porous cross-linked human collagen Matrix or Sponge, used as a scaffold in the repair and restoration of dura mater defects, following craniotomy, laminectomy or in general when there is intentional (surgical procedure) or accidental damage to the dura mater.

Treatment:

Device: Human collagen matrix graft

Bovine collagen matrix graft

Description:

Is a porous type 1 collagen matrix derived from bovine Achilles tendon, this matrix is absorbed after 8 weeks and is used for the repair and restoration of dura mater defects.

Treatment:

Device: Bovine collagen matrix graft