Laparoscopic Ventral Hernia Repair with Routine Defect Closure Using Su2ura® Approximation Device

NCT ID: NCT04986917

Last Updated: 2025-01-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-19
• Study Completion Date: 2024-11-21

Brief Summary

Study includes 5 visits: Screening, Baseline/Surgery, and 14 days, 3 months, 12months Follow-Ups post-surgery. The actual point of enrollment for each subject is considered the day of surgery. Total study duration is up to 12 months post-surgery.

Surgery will be performed under general anesthesia. Standard antibiotic prophylaxis will be administered 30 min prior to skin incision. A surgical assistant will be selected by the PI from the surgical staff of the department.

The procedure will involve placement of laparoscopic ports, reduction of the hernia sac, closure of the defect with the Su2ura® approximation device and fixation of mesh with tacks over the closed defect in an IPOM fashion.

Based on surgeon consideration, primary umbilical hernia defects under 2 cm will be repaired with or without mesh.

Study follow-up visits will take place 14 days, 3 months and 12 months post-surgery.

Detailed Description

This study will be performed in accordance with the design and specific provisions of this protocol, in accordance with the ethical principles that have their origin in the Declaration of Helsinki, that are consistent with Good Clinical Practice (GCP), Title 21 of the Code of Federal Regulations (21 CFR), part 812 (Investigational Device Exemptions), and the applicable regulatory requirements.

The study is a prospective, multi-center, open study, to evaluate the efficacy and safety of the Su2ura® approximation device.

An abdominal hernia emerges through a preformed or acquired defect of the abdominal wall. The defect may be congenital (primary), acquired as a result of wear and tear (primary), or result from surgery or trauma, where failure of the abdominal wall to heal produces an incisional (non-primary) hernia. Examples of abdominal hernia include epigastric, umbilical and inguinal hernia. Patients may be asymptomatic or complain of a lump or pain. These patients are offered elective surgery. Patients may also present with complications necessitating emergency repair with or without additional resection of compromised viscera.

Ventral hernias are very common and do present a challenge because of the risk of recurrence. Besides the surgeon, these hernias are ideally managed by a dietitian, nurse, and a physical therapist. Patient education has been a very popular topic in literature and hospital settings. Giving patients literature and discussing outcomes with instructions on multiple aspects throughout their encounters has shown to be very effective.

The Su2ura Approximation Device is designed to deploy anchors threaded with stiches to facilitate tissue approximation by eliminating the need for the passing of a needle from one side of the tissue to the other as performed in traditional suturing. Utilizing the anchor feature allows a single action placement of a suture.

The principal investigator from each medical center participated in an appropriate training program. This training included the surgery procedure in an animal. The Principal investigators will train the sub investigators in this procedure. The sponsor will also provide training on the laparoscopic simulator to the principal investigators.

A total of 60 patients will be recruited to the study. Patients with a primary umbilical hernia under 2 cm will be recruited to the study and the hernia will be repaired with or without mesh according to the PI's decision.

Eligible patients with a primary or secondary ventral hernia, desiring an elective surgical repair, who amply the inclusion/Exclusion criteria will be offered to participate in the study.

Study includes 5 visits: Screening, Baseline/Surgery, and 14 days, 3 months, 12months Follow-Ups post-surgery. The actual point of enrollment for each subject is considered the day of surgery. Total study duration is up to 12months post-surgery.

Conditions

Ventral Hernia

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Su2ura® approximation device - study device group

Patients with a primary umbilical hernia will be recruited to the study and the hernia will be repaired using the Su2ura® approximation device

Group Type: EXPERIMENTAL

Hernia repair surgery using the Su2ura® approximation device

Intervention Type: DEVICE

. The hernia defect will be measured and the Su2ura® approximation device will then be used to close the defect, placing stainless steel implantable anchors threaded on a Polyethylene braided surgical suture.

Physical Examination

Intervention Type: DIAGNOSTIC_TEST

All subjects will undergo a standard physical examination by an authorized physician. The physician's evaluation will include diagnosis and documentation of any significant clinical abnormalities or diseases.

Vital Signs

Intervention Type: DIAGNOSTIC_TEST

Vital signs include blood pressure, pulse, temperature, body weight and height, body mass index (BMI).

Blood Tests

Intervention Type: DIAGNOSTIC_TEST

All subjects will undergo Hematology and Biochemistry blood tests. Blood Hematology test will include a complete CBC. Blood Biochemistry test will include the following measures: Sodium (Na), Potassium (K), Chloride (Cl), Creatinine, Glucose, Urea, Albumin, Calcium total, Alkaline Phosphatase (ALP), ALT, AST, Total Bilirubin, Direct Bilirubin, LDH, Total Protein, Uric Acid, CRP, and Lipid Profile (including Total Cholesterol, HDL, LDL, Triglycerides).

5 ml of blood (equals to 1 spoon) will be taken for each test.

Urine Pregnancy Test

Intervention Type: DIAGNOSTIC_TEST

Urine pregnancy test will be performed during the screening visit (for WOCBP).

Abdominal Ultrasound imaging

Intervention Type: DIAGNOSTIC_TEST

All subjects will undergo an abdominal ultrasound (US) imaging at 12 Months visit. The US will be performed to verify an absence of hernia recurrence.

EuraHS-QoL

Intervention Type: OTHER

patients will be asked to fill a questionnaire assessing patient-reported satisfaction and function. questionnaire score range: 0-180; higher score indicates higher pain and discomfort

Visual Analouge Scale (VAS)

Intervention Type: OTHER

A validated, subjective measure measuring acute and chronic pain. questionnaire score range: 0-10; higher score indicates higher pain level.

Clinical evaluation for hernia recurrence and clinical bulging

Intervention Type: DIAGNOSTIC_TEST

The procedure includes:

1. Clinical examination to determine the presence of hernia recurrence and clinical bulging, in an inconclusive physical exam a radiological imaging will be performed such as US or CT.

2. SAE's and SADE's evaluation of the seroma.

3. Taking a photograph of the surgery area without disclosing the subject's identity.

Interventions

Hernia repair surgery using the Su2ura® approximation device

. The hernia defect will be measured and the Su2ura® approximation device will then be used to close the defect, placing stainless steel implantable anchors threaded on a Polyethylene braided surgical suture.

Intervention Type: DEVICE

Physical Examination

All subjects will undergo a standard physical examination by an authorized physician. The physician's evaluation will include diagnosis and documentation of any significant clinical abnormalities or diseases.

Intervention Type: DIAGNOSTIC_TEST

Vital Signs

Vital signs include blood pressure, pulse, temperature, body weight and height, body mass index (BMI).

Intervention Type: DIAGNOSTIC_TEST

Blood Tests

All subjects will undergo Hematology and Biochemistry blood tests. Blood Hematology test will include a complete CBC. Blood Biochemistry test will include the following measures: Sodium (Na), Potassium (K), Chloride (Cl), Creatinine, Glucose, Urea, Albumin, Calcium total, Alkaline Phosphatase (ALP), ALT, AST, Total Bilirubin, Direct Bilirubin, LDH, Total Protein, Uric Acid, CRP, and Lipid Profile (including Total Cholesterol, HDL, LDL, Triglycerides).

5 ml of blood (equals to 1 spoon) will be taken for each test.

Intervention Type: DIAGNOSTIC_TEST

Urine Pregnancy Test

Urine pregnancy test will be performed during the screening visit (for WOCBP).

Intervention Type: DIAGNOSTIC_TEST

Abdominal Ultrasound imaging

All subjects will undergo an abdominal ultrasound (US) imaging at 12 Months visit. The US will be performed to verify an absence of hernia recurrence.

Intervention Type: DIAGNOSTIC_TEST

EuraHS-QoL

patients will be asked to fill a questionnaire assessing patient-reported satisfaction and function. questionnaire score range: 0-180; higher score indicates higher pain and discomfort

Intervention Type: OTHER

Visual Analouge Scale (VAS)

A validated, subjective measure measuring acute and chronic pain. questionnaire score range: 0-10; higher score indicates higher pain level.

Intervention Type: OTHER

Clinical evaluation for hernia recurrence and clinical bulging

The procedure includes:

1. Clinical examination to determine the presence of hernia recurrence and clinical bulging, in an inconclusive physical exam a radiological imaging will be performed such as US or CT.

2. SAE's and SADE's evaluation of the seroma.

3. Taking a photograph of the surgery area without disclosing the subject's identity.

Intervention Type: DIAGNOSTIC_TEST

Other Intervention Names

study device intervention; (hernia-specific European Hernia Society Quality of Life Questionnaire)

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 years.

2. Patient desires an elective surgical repair.

3. Patient is able to provide an informed consent.

4. Diagnosis of a primary or secondary ventral hernia, with a fascial defect of width no more than 5 cm width in size on clinical examination or imaging scan.

5. Body mass index (BMI) of 20-40 kg/m2.

6. Candidate for laparoscopic repair based on the operating surgeon's assessment.

Exclusion Criteria

2. Patient in need of concomitant non-hernia repair surgical procedure(s). 3. Patient in need of emergent ventral hernia repair for complications such as incarceration, intestinal obstruction or strangulation.

4. The patient desires hernia repair using a technique other than that consistent with the study.

5. Patient has loss of domain as assessed on physical examination or CT scan. 6. Patient has a history of an abdominal aortic aneurysm repair. 7. Patient has a severe co-morbid condition likely to limit survival to less than 2 years.

8. Patient was treated with chemotherapy in the past 6 months. 9. Patient was treated with steroids in the past 6 months. 10. Patient with known collagen disorder. 11. Clean contaminated/contaminated or dirty surgical field. 12. Patient is pregnant or intends to become pregnant during the study period. 13. Patient has ascites on physical examination or CT scan. 14. Patient has liver failure. 15. Patient undergoing dialysis treatment. 16. Patient has a wound-healing disorder. 17. Patient has an untreated coagulation disorder or is on anti-coagulant therapy not managed peri-operatively with the advice or supervision of a hematologist.

18. Patient with autoimmune disorder requiring more than 10 mg of corticosteroid daily.

19. Patient who is immunocompromised (including a diagnosis of HIV/AIDS, organ transplant, or receiving chemo- or radiation therapy.

20. Patient in need of concomitant surgical procedures other than indicated in the protocol as acceptable.

21. Non-compliance with the study protocol. 22. Patient requests to exit the study. 23. Prior radiotherapy. 24. Active malignancy for at least 2 years. 25. Patients has Diastasis recti more than 4cm×4cm size

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Anchora Medical

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hillel Yaffe Medical Center

Hadera, Central District, Israel

Barzilai Medical Center

Ashkelon, Southern District, Israel

Countries

Israel

Other Identifiers

ANC-002

Identifier Type: -

Identifier Source: org_study_id