Evaluation of Zip Device to Conventional Sutures for Laceration Repair in Pediatrics in an Emergency Department

Laceration of Skin Clinical Trial

— ZIPPED  

Official title:

A Randomized, Controlled, Post-market Clinical Investigation to Evaluate Zip Surgical Skin Closure Device in Comparison of Using Standard of Care Sutures for Laceration Repair in Pediatrics in an Emergency Department

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04122859
• Other study ID #: 012
• Status: Recruiting
• Phase: N/A
• Start date: November 1, 2018
• Est. completion date: July 31, 2020

Study information

• Verified date: October 2019
• Source: ZipLine Medical Inc.
• Contact: Eric Storne
• Phone: 408.684.0747
• Email: estorne[@]ziplinemedical.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A prospective, randomized, controlled post-market clinical investigation that will enroll pediatric subjects requiring laceration repair. The investigation population will consist of 30 subjects fulfilling the eligibility criteria for the clinical investigation. The subjects will be randomly assigned at a 1:1 ratio to either the Zip 4 Surgical Skin Closure Device group or the Standard of Care sutures group.

Description:

The commercial use of the Zip device has demonstrated applicability and acceptance in many medical specialties, including laceration closure in the Emergency Department setting. However, while clinical studies have demonstrated quantitative performance benefits of the device in orthopedic, dermatology, cardiac and cardiology specialties, no quantitative studies have been conducted in the Emergency Department setting with the device with which emergency medicine physicians may make quantitative, informed treatment choices. The Sponsor (ZipLine Medical) and the study doctor (investigator) have furthermore identified the pediatric patient population presenting for laceration repair in the Emergency Department as a group that may uniquely benefit from the use of the Zip device.

Standard care for wounds of this type require cleaning the wound, anesthetizing the wound and closing the wound with sutures that typically require subsequent removal at a later date. The Zip device is non-invasive and therefore requires no injected anesthesia or sedation for wound closure. In addition, the referenced clinical studies have demonstrated at least a 3 times speed advantage over sutures. The Zip device ease of use and consistency of outcomes enables less skilled or experienced caregivers to perform fast, efficient and excellent wound closure, which can improve department and staff efficiency, patient throughput and overall patient satisfaction. Finally, the Zip device may be removed by the patient or parent at home, eliminating a return-to-clinic visit for removal.

ZipLine Medical believes that the demonstrated benefits of the Zip device will be more pronounced with the specified pediatric population due to reduced procedure time, elimination of injected anesthesia and elimination of a return visit for suture removal. ZipLine Medical believes that this will reduce fear and anxiety in pediatric patients. Furthermore, ZipLine Medical believes that the Zip device can improve Emergency Department efficiency and patient throughput, reduce overall healthcare cost and improve overall patient (and parent) satisfaction.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: July 31, 2020
• Est. primary completion date: July 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years to 14 Years

Eligibility

Inclusion Criteria:

1. Between 4 to 14 years of age at the time of laceration repair.

2. Require suture closure as standard of care for simple straight wounds on trunk or extremities up to 4 cm long.

3. Low Tension Laceration, e.g. skin can be easily approximated by pinching with fingers.

4. Subject and legal representative(s) are willing and able to comply with the investigational device removal and meet the follow up visit requirements.

5. Subject and legal representative(s) have been informed of the nature, the scope and the relevance of the study.

6. Subject and legal representative(s) have voluntarily agreed to participation and have duly signed the Informed Consent Form.

Exclusion Criteria:

1. Known personal or familial history of scar hypertrophy.

2. Known or suspected allergies or hypersensitivity to non-latex skin adhesives.

3. Atrophic skin deemed clinically prone to blistering.

4. Wounds that are easily susceptible to infection as a result of exposure to unsanitary conditions ("dirty wounds").

5. Wounds that require deep dermal closure using sutures.

6. Known or suspected mental problems and/or aggressiveness that indicates that the subject might try to remove the device during the treatment period.

7. Participating in any other clinical investigation.

8. Known health condition that would affect healing in the opinion of the investigator.

9. Any subject that according to the Declaration of Helsinki is deemed unsuitable for study enrollment.

Related Conditions & MeSH terms

• Emergencies
• Laceration of Skin
• Lacerations

Intervention

Device:
• Zip Skin Closure Device
The device is a CE-marked, single use, sterile medical device that is designed to provide closure speed superior to sutures, while resulting in a suture-like cosmetic outcome. It adheres to the skin adjacent to an incision or laceration by use of pressure-sensitive skin adhesives.

Locations

Country	Name	City	State
Israel	Kaplan Medical Center	Re?ovot

Sponsors (1)

Lead Sponsor	Collaborator
ZipLine Medical Inc.

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean difference in time to wound closure of the Zip 4 Surgical Skin Closure Device in comparison to conventional sutures used in a pediatric population presenting for laceration repair.	These include total treatment time and duration of period starting from the preparation of procedure until protective wound dressing is applied, and including whether or not anesthesia and/or sedation was used when comparing the Zip 4 Surgical Skin Closure Device and the standard of care closure suturing	Intra operative
Secondary	Difference in Wound Evaluation Score (WES)	A Wound Evaluation Score will be documented by an independent reviewer of photos taken at Day 0 and compared to 10 Day and 30 Day to evaluate the satisfaction and outcomes of the Zip 4 Surgical Skin Closure Device in comparison to conventional sutures used in a pediatric population presenting for laceration repair. The WES evaluates six clinical variables including incision edges, contour irregularity, width, edge inversion, inflammation and overall cosmesis. A score of 6 is considered optimal, while a score of < or =5 suboptimal.	10 days and 30 days post laceration repair
Secondary	Satisfaction of Rate of Wound Healing of Laceration Repair:satisfaction rating	Parents of patients will document the rate of wound healing satisfaction in subject post-treatment. The satisfaction rating for the Zip 4 Surgical Skin Closure Device will be compared to conventional sutures used in a pediatric population for laceration repair. The questionnaire will contain questions where the parent either will mark the most correct answer or rate on a line between 0 (Very Satisfied) to 100 (Very Dissatisfied) mm.	30 days post laceration repair
Secondary	Pain Level for Wound Healing of Laceration Repair: visual analog scale (VAS)	Parents of patients will document the level of pain the patient experiences in connection to the Zip 4 Surgical Skin Closure Device and conventional sutures application and removal used in a pediatric population for laceration repair by a visual analog scale (VAS) 0 (No Pain) -100 (Worst Pain) mm	Day 0 and 10 days post laceration repair
Secondary	Safety by Adverse Events reported that relate to the study device	The incidence and severity of adverse events associated with the Zip 4 Surgical Skin Closure Device and Standard of Care closure sutures.	Intra operative through the end of the study at 30 days post laceration repair