A Safety and Effectiveness Study of DividPro Film in Open Abdominal Surgery

Industrial Technology Research Institute, Taiwan

Status

Enrolling

Conditions

Abdominal Adhesion

Open Abdominal Surgery

Treatments

Device: DividPro film

Study type

Interventional

Funder types

Other

Identifiers

NCT06142526

ITRIDP20220510

Details and patient eligibility

About

Abdominal adhesions frequently occur after surgery and may be one of the main reasons to cause discomfort, pain and related bowel movement symptoms. The goal of this clinical trial is to evaluate the safety of DividPro film and its potential effectiveness for reducing the incidence of abdominal adhesion. Treatment group will have DividPro film implantation right before the closure of surgical incision wound. Control group will have standard care without any anti-adhesion related products. In addition to adverse event assessment and safety lab tests, participants will accept abdominal ultrasound and quality of life questionnaire at each visit for effectiveness evaluation.

Full description

Adhesion may occur due to the excessive production of fibrous tissue during the process of wound healing. Abdominal adhesion could play a role on intestine obstruction which will lead to lack of blood flow to the blocked part of the intestine or peritonitis. Improving surgical skills, cleaning wound before closure or using physical barrier between the incision site and abdominal wall can lower the incidence of abdominal adhesion.

In this study, participant who meets the eligibility criteria will be enrolled and randomized to either the treatment or control group. During the surgery period, subject will have the DividPro film implantation or only the standard care procedure right before the closure of the surgical wound. Participants will be instructed to return for visits on day 7, month 1, 3, 6 and 12. Adverse event, clinical laboratory test, vital sign and physical examination will be tested and recorded during the course of the study as the items of safety assessment. In addition, symptom related to tissue adhesion, visceral sliding test and quality of life questionnaire will also be assessed as the parameters of efficacy at the predetermined time points throughout the study .

Enrollment

60 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Written informed consent before any study specific procedure is performed.
Ages of 20-70 years old on the day of consent.
Subject who is diagnosed with a liver, gallbladder, pancreas and upper/lower gastrointestinal disorder.
Subject who is scheduled to accept an open abdominal operation involving liver, gallbladder, pancreas, stomach, spleen, intestine or female pelvic organ.
The Investigational product can be implanted appropriately between the surgical wound and operated organ and is able to cover the entire wound area.

Exclusion criteria

Subject who is hypersensitive to the ingredient of DividPro film [Poly (DL-lactide)]
Subject who is concurrently participating in another clinical trial with a drug or a device.
Subject who has taken Immunosuppressive drugs/agents long-term or taken NSAIDs within 7 days before trial's operation.
Subject who has participated in a clinical trial with a drug or a device within 30 days prior to this study.
Subject who has received or is expected to receive any other product or technique belonging to the group of adhesion reduction devices or other products, meshes, or other types of implants in the abdominal cavity within 30 days prior to or during enrollment.
Subject who has had hernia mesh placed under the abdominal wall.
Subject with peritonitis.
Subject with hematological, neurological or immune critical illness.
Subject who has malnutrition, uncontrolled diabetes or any other conditions that the investigator considers might not be suitable for enrollment to the study.
Subject with other potential infections.
Subject with BMI≧40.
Female subject who is lactating or pregnant.