VistaCare® in the Treatment of Wounds of the Lower Extremity

Wound Heal Clinical Trial

Official title:

Open Label Assessment of VistaCare® Treatment in Current Medical Practice in Patients With Acute and Chronic Leg Wounds.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03790202
• Other study ID #: VistaCare® OPEN PMCF
• Status: Completed
• Start date: February 18, 2019
• Est. completion date: February 1, 2021

Study information

• Verified date: February 2021
• Source: DTAMedical SAS
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Assessment of the safety and performance of the VistaCare® medical device in current medical practice in the treatment of acute and chronic lower limb wounds.

Description:

The study is an open-label, prospective, multicenter, post-CE mark (European Conformity assessment indicating marketing approval in Europe) study to assess the safety and performance of the VistaCare® device in the treatment of wounds. The duration of patient follow-up is up to 30 days, with intermediate visits at 3, 7, 15 and 30 days following initiation of treatment with the device.

Up to 30 patients will be recruited in the trial. Assessments will include clinical status, wound status, standardized photography, TcPO2 (trans-cutaneous oxygen pressure assessment) in a study sub-population, visual analogy scales to assess pain and comfort and adverse events monitoring.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: February 1, 2021
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• male or female consenting and able patients aged 18 or more affiliated to social security

• presenting with acute or chronic traumatic or surgical lower limb wounds (excluding tumoral excision)

• presenting with no intercurrent pathology which in the opinion of the investigator may interfere with the capacity for wound healing

• patients whose wound is compatible in terms of location with VistaCare treatment

• patient whose wound has a minimal surface of 10 cm2

• patient whose wound does not need surgical Peterson after inclusion (if needed should be performed prior to inclusion)

Exclusion Criteria:

• Female patients pregnant, lactating, or of childbearing age and not using adequate contraception (pregnancy test mandatory)

• patients incapable of making an informed decision about participation

• patients presenting a condition that interferes with adequate wound healing capacity (uncontrolled diabetes, heavy smokers, auto-immune disease)

• concurrent treatment or treatment within one month prior to inclusion with local or systemic corticosteroids, immunosuppresseurs, chemotherapy or radiotherapy

• wound location incompatible with VistaCare

• general infection signs at the time of inclusion (fever, lymphangitis, pus ...)

• patients presenting with important uncontrolled hemorrhage at the time of inclusion

• patients previously recruited into this trial or any other trial within 1 month, or currently in the exclusion timeframe of another trial

• patients with a wound surface less than 10 cm2

• patient with a would previously treated with hyperbaric chamber

• legally incapacitated, under guardianship or psychiatric patients

• emergency condition prohibiting adequate patient consent prior to inclusion

Related Conditions & MeSH terms

• Wound Heal
• Wounds and Injuries

Intervention

Device:
• VistaCare®
Controlled atmosphere wound healing device

Locations

Country	Name	City	State
France	CHU Henri Mondor	Créteil
France	Hôpital de la Conception	Marseille
France	Hôpital La Timone	Marseille
France	Hôpital La Timone	Marseille
France	CHU de Nantes Centre des Brûlés	Nantes

Sponsors (1)

Lead Sponsor	Collaborator
DTAMedical SAS

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of the global Safety of use of the VistaCare® medical device in standard medical practice	Assessment of the global safety of VistaCare® in current medical practice in patients with acute or chronic lower limb wounds through monitoring of concurrent averse events throughout the study duration. This will be assessed through the frequency of occurrence of device-related events, throughout the patient's participation in the trial	up to 30 days
Primary	Assessment of the global Performance of the VistaCare® device in standard medical practice	Assessment of the global performance of the VistaCare® medical device as compared to its labeled performance in the approved indication (wound healing). This will be assessed through a global clinical assessment by the investigator of the wound improvement condition throughout the study visits, measured in 3 grades ranging from Aggravation (worst assessment), through Static (no improvement) to Improved (best assessment), taking into consideration the wound healing stage and general clinical condition per investigator's assessment.	up to 30 days
Secondary	Assessment of time under VistaCare treatment till secondary treatment decision	Assessment of the time in days till decision to wound coverage, graft, wound dressing, or no further treatment needed and patient discharge. Duration in days from VistaCare treatment initiation to decision-making will be tabulated for each patient.	up to 15 days
Secondary	Wound surface calorimetric assessment of wound status	Description of wound clinical status evolution through photography, wound measurement in mm2 and visual assessment of wound status. This measure is based on the surface in mm2 of the wound components on a standard photography, each wound potentially comprising 3 wound stages surfaces : necrotic (worst), granulation and epithelization (most favorable wound healing stage). Those stages are measured on each visit on a standardized photography of the wound and the wound stage evolution in time is assessed for each patient by an external reviewer. Wound staging for each patient will be analyzed in time throughout patient's participation and presented as graphs.	30 days
Secondary	Safety assessment of the VistaCare® treatment through monitoring of the frequency of adverse events	Safety assessment of the VistaCare® treatment through adverse events monitoring, with frequency of patients presenting with any adverse event and frequency of each adverse event type, namely non-serious unrelated or device-related event (respectively AE, ADE), serious unrelated event (SAE), serious device-related event (SADE), unanticipated device-related event (UADE), or device deficiency. Tabulation of frequencies in percentages of patient occurrence and number of events per patient will be provided.	throughout 30 days
Secondary	TcPO2 assessment	In a sub-group of up to 10 patients, measure of the trans-cutaneous oxygen pressure (TcPO2) around the wound to assess status and potential correlation with wound status. This measure is expressed in mmHG and the correlation between this measure and the wound healing stage will be statistically assessed to indicate if wound healing may be correlated to the oxygen pressure measure.	up to 30 days
Secondary	Quality of Life assessments	Patient visual analogy scale (VAS) assessments of pain and comfort. Those scales are each graduated from 0 (none) to 10 (maximum pain or discomfort). The evolution in times of such scores will be statistically assessed for each patient.	throughout 30 days
Secondary	Duration of hospitalization	Assessment of the total duration of patient hospitalization in days.	throughout 30 days

External Links

•   Sponsor's internet site