Post Approval Study to Evaluate the Safety and Performance of GENTA-FOIL Resorb® in Hand Surgery

Tissue Adhesions, Surgery-Induced Clinical Trial

Official title:

Post Approval Study to Evaluate the Safety and Performance of GENTA-FOIL Resorb® for the Prevention of Tissue Adhesions in Hand Surgery

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04482140
• Other study ID #: 001GF
• Status: Not yet recruiting
• Start date: April 2024
• Est. completion date: July 2025

Study information

• Verified date: January 2024
• Source: Advanced Medical Solutions Ltd.
• Contact: Susan Clark
• Phone: 01606863500
• Email: susan.clark[@]admedsol.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Single arm study to evaluate the safety and performance of Genta-Foil resorb® for the prevention of tissue adhesions

Description:

GENTA-FOIL resorb® is an implantable, absorbable collagen barrier foil, which forms a temporary barrier between the functional structures during the critical phase of wound healing. As a result, the ability of the tissue layers to slide against each other is retained.

The objective of hand surgery is to promote wound repair, and regeneration of all motor and sensory functions of the hand and to restore the subject's hand mobility, and improve their quality of life. However, hand trauma and operations often lead to the formation of adhesions between the various tissue layers of the hand (e.g. muscles, tendons and nerves). Even with minimally invasive procedures and optimal aftercare, development of adhesions in the suture and wound areas is often unavoidable. Adhesion formation between repaired tendons and the surrounding tissue has been thought to be one of the most important factors that disturbs functional restoration. It is estimated that the adhesion, which can cause significant disability, occurs in about 30% of cases.

The purpose of this study is to investigate the use of GENTA-FOIL resorb® for the prevention of tissue adhesions measured by restoration in digital function in subjects undergoing hand surgery. The functional outcome of tendon injury after a repair depends on multiple factors such as age, injury level and type, type of repair, and post repair therapy.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 55
• Est. completion date: July 2025
• Est. primary completion date: July 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subject is male or female, =18 years of age;

2. Subject is willing and able to give written informed consent;

3. Subject is scheduled for one if the following surgical procedures:

• 3a. extensor tendon repair zones I to VI.

• 3b. flexor tendon repair zones I to VI.

• 3c. open reduction and internal fixation to repair hand fractures of proximal phalanx, and/or middle phalanx, and/or metacarpals

4. Subject is willing and able to comply with the study procedures during surgery and the post-surgical follow up period.

Exclusion Criteria:

1. Subject is known to be sensitive to any of the device components e.g. Gentamicin (aminoglycosides) or equine collagen.

2. Subject is known to be non-compliant with medical treatment.

3. Subject has any known impaired renal function/autoimmune illness/neuromuscular disease (such as Parkinson's or Myasthenia Gravis).

4. Subject is currently taking an Aminoglycoside antibiotic as stand-alone treatment or in combination with other antibiotics

5. Subject is pregnant or actively breastfeeding.

6. Subject has active infection at surgical site

7. Subject has any significant or unstable medical or psychiatric condition that, in the opinion of the Investigator, would interfere with their ability to participate in the study, or affect the study outcomes.

8. Subject is currently enrolled in another clinical study that would interfere with their ability to participate in this study

Related Conditions & MeSH terms

• Tissue Adhesions
• Tissue Adhesions, Surgery-Induced

Intervention

Device:
• Genta-Foil resorb®
Use of Genta-Foil resorb® to prevent adhesions in patients undergoing hand surgery

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Advanced Medical Solutions Ltd.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Restoration of hand mobility	Restoration of hand mobility will be assessed using functional assessment scoring Total Active Motion (TAM) at 90 days post-surgery. This will be measured by the modified Strickland scoring criteria. The success criteria is defined as TAM score of 75% or above at 90 days post-surgery. Restriction of TAM post-surgery is indicative of tissue adhesions, therefore this measure will demonstrate presence / absence of of tissue adhesions.	At 90 days post-surgery
Secondary	Incidence of device related infections at surgical site up to 30 days post-surgery.	As per local Standard of Care wound assessment, absence or presence of wound signs infection will be recorded.	Up to 30 days post-surgery
Secondary	Incidence of device related adverse events	Evaluation of safety of GENTA-FOIL resorb® by recording of any device or procedure-related adverse events throughout the surgery during the follow-up period (day of surgery, at 7 days, 14 days, 30 days and 90 days post-surgery)	Up to 90 days post-surgery
Secondary	Subjective assessment of symptoms and abilities to perform activities by 90 days post-surgery	Study subjects requested to self assess symptoms and abilities to perform activities by 90 days post-surgery. Subjects will be asked to complete the standardised QuickDASH upper extremity outcome measure questionnaire. QuickDASH Outcome Measure tool measures the individual's ability to complete tasks at home and severity of symptoms. The tool uses 11 questions and a 5-point Likert Scale from which the patient can select an appropriate number corresponding to their severity / function level.	At 90 days post-surgery
Secondary	Wound healing without complications up to 30 days post-surgery.	Standard of Care wound assessments will be performed at follow-up visits at day 7, day 14 and day 30 as appropriate, by a designated member of the Hand Dressing Clinic as per local Outpatient Wound Assessment Tool. As part of wound assessment, date of when wound is healed will be recorded during appropriate follow-up visit.	Up to 30 days
Secondary	Change in patient pain scores (assessed using VAS) up to 90 days post-surgery.	Severity of localised pain in the affected hand or finger(s) will be measured using a Visual Analogue Scale (VAS). The VAS will be a 10cm horizontal line, with descriptors at each end [no pain (0cm), and worst imaginable pain (10cm)]. Subjects will be asked to place a mark on the scale that corresponds to their pain. The distance from the lower end of the scale will be measured and recorded.	Up to 90 days post-surgery
Secondary	Clinicians' satisfaction with the device at time of surgery	Assessment of satisfaction with device conformability and ease of use. Assessed using a Likert-type scale.	Immediately post-surgery