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Healing Rate of Leg Wounds Treated With Contact and Noncontact Ultrasound: The VIP Ultrasound Protocol

Primary Purpose

Chronic Ulcer of Lower Extremity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Contact Ultrasound Therapy
Noncontact Ultrasound Therapy
Sponsored by
Texas Health Resources
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Ulcer of Lower Extremity focused on measuring Sub-acute wound, Chronic wound, Wound, MIST, Soring, Contact Ultrasound, Noncontact ultrasound, Wound Care, VIP Ultrasound Protocol, Ultrasound

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient is referred to Physical Therapy for contact ultrasound (which is included in the VIP protocol);
  • Lower extremity (including foot) wound(s) of any etiology;
  • Wound(s) presenting with slough, necrotic tissue, and/or non-viable tissue requiring debridement;
  • Wound is present for 4 weeks or longer at the start of ultrasonic therapy;
  • Insurance approval is obtained for Contact and Noncontact ultrasound treatments, in the ambulatory setting;
  • Patient is 18 years of age or older;
  • Female patient attesting not to be pregnant;
  • Not undergoing Vacuum Assisted Closure (VAC) therapy.

Exclusion Criteria:

  • Patient is referred to Physical Therapy for noncontact ultrasound only;
  • Wound(s) not on lower extremity;
  • Clean wound(s) that do not require debridement;
  • Wound onset less than 4 weeks prior to the start of ultrasonic therapy;
  • Malignancies on the treatment area;
  • Patients in the ambulatory setting whose insurance did not approve them for both contact and noncontact ultrasound therapy;
  • Patient is under 18 years of age;
  • Female patient attesting to be pregnant;
  • VAC Therapy.

Sites / Locations

  • Texas Health Resources - Presbyterian Hospital of Dallas

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ambulatory Wound Clinic

Arm Description

Intervention with contact ultrasound therapy and noncontact ultrasound therapy following the study protocol on subjects receiving care at the wound clinic.

Outcomes

Primary Outcome Measures

Total Wound Area
Mean and Standard Deviation of the group's total wound area at day one and last treatment day. Wound area was measured as Length x Width. This is to assess the change in area, in order to assess wound progress towards closure.

Secondary Outcome Measures

Total Wound Volume
Mean and Standard Deviation of the group's total wound volume at day one and last treatment day. Wound volume was measured as Length x Width X Depth (when able to determine depth). This is to assess the change in volume, in order to assess wound progress towards closure.
Wounds With Slough/Eschar Reduction on Visit 2 and Wounds With Slough/Eschar Reduction at Last Visit
Mean and Standard Deviation of the group's percent adherent and/or non-adherent slough present in the wound bed at day one and last treatment day. This is to assess the change in slough/eschar. This is to determine progression from contact to noncontact ultrasound therapy, as well as to determine progress of wound bed quality.

Full Information

First Posted
January 20, 2014
Last Updated
January 20, 2022
Sponsor
Texas Health Resources
Collaborators
Celleration, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02045303
Brief Title
Healing Rate of Leg Wounds Treated With Contact and Noncontact Ultrasound: The VIP Ultrasound Protocol
Official Title
Healing Rate of Chronic and Sub-Acute Lower Extremity Ulcers Treated With Contact Ultrasound Followed by MIST Therapy: The VIP Ultrasound Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas Health Resources
Collaborators
Celleration, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Wound healing rate is higher when contact ultrasound therapy is followed by noncontact ultrasound therapy on sub-acute and chronic lower extremity ulcers of various etiologies requiring selective debridement, as compared to either Sonoca-180 or MIST Therapy alone.
Detailed Description
This prospective pilot study is designed to evaluate the clinical effectiveness of a wound care ultrasound treatment protocol for sub-acute or chronic wounds of the lower extremity and of any etiology. The Viana-Pompeo (VIP) ultrasound protocol consists of high intensity, low frequency, contact ultrasound therapy (with Sonoca-180) followed by low intensity, low-frequency, noncontact ultrasound therapy (with MIST Therapy). Previously published healing rates for each of the ultrasonic therapy modalities will be used as a comparison. The Physical Therapist will perform the initial assessment and treatment, and devise an individualized plan of care that involves contact ultrasound followed by noncontact ultrasound. Subjects may remain in the study for up to 12 weeks, or up to when end of study criteria is met. Transition from contact mode to noncontact mode will happen when: - Wound is sufficiently clean with ≤ 20% of necrotic tissue or adherent slough. OR - >= 80% of soft slough is easily removed from the wound bed with mechanical or selective debridement before or after treatment OR - Wound bed quality has failed to progress after 3 consecutive contact ultrasound treatments For the purposes of this study, treatments will be performed 3 times a week. Treatment time will be dependent on the wound area, at least 20 sec/cm2, per standard protocol. Only the wounds present during Physical Therapy (PT) initial assessment will be included in the research. If the patient develops new wounds during the course of the research, the patient will receive appropriate treatment, but such wounds will not be part of the study. Patients in the wound clinic setting are allowed to perform home dressing changes as ordered by the physician in addition to the dressing changes performed by the therapist or wound clinic nurse on clinic visit days. Patients and/or caregivers will be trained in dressing changes techniques and must understand the procedure prior to performing dressing changes on their own. In addition to ultrasonic treatment and dressing changes, wound debridement may be performed each visit as needed. Digital photography and wound measurements will also be performed weekly and as needed. End of PT wound therapy may be before, at, or after the end of the study period. The beginning of the MIST therapy will depend on the individual characteristics and wound needs. A minimum of 4 MIST treatments must be completed for a patient's data to be included the data analysis in the acute care setting. A minimum of 2 treatments per week (goal of 3 per week) must be reached for the 12 week period for a patient's data to be included in the data analysis. Study Endpoints Primary endpoint: Wound area reduction Percent granulation tissue Length of the study for ambulatory subjects: 12 weeks from Start of Contact Ultrasound therapy Secondary endpoint: Wound closure at any point within the length of study Failure to note improvement in wound area, and/or wound volume, and/or wound bed quality after 4 consecutive weeks of treatment. 3 consecutive missed visits, or a total of 7 missed visits

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Ulcer of Lower Extremity
Keywords
Sub-acute wound, Chronic wound, Wound, MIST, Soring, Contact Ultrasound, Noncontact ultrasound, Wound Care, VIP Ultrasound Protocol, Ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ambulatory Wound Clinic
Arm Type
Experimental
Arm Description
Intervention with contact ultrasound therapy and noncontact ultrasound therapy following the study protocol on subjects receiving care at the wound clinic.
Intervention Type
Device
Intervention Name(s)
Contact Ultrasound Therapy
Other Intervention Name(s)
Soring, Sonoca-180
Intervention Description
Following our protocol, the ultrasound wound therapy will start with contact ultrasound until it meets criteria to switch to noncontact ultrasound therapy.
Intervention Type
Device
Intervention Name(s)
Noncontact Ultrasound Therapy
Other Intervention Name(s)
Celleration Inc, MIST Therapy
Intervention Description
Transition from contact to noncontact ultrasound when criteria for transition is met per our protocol.
Primary Outcome Measure Information:
Title
Total Wound Area
Description
Mean and Standard Deviation of the group's total wound area at day one and last treatment day. Wound area was measured as Length x Width. This is to assess the change in area, in order to assess wound progress towards closure.
Time Frame
Initial measurement at day 1 and measurement at the subject's last visit at 12 weeks or sooner if the wound closed before then.
Secondary Outcome Measure Information:
Title
Total Wound Volume
Description
Mean and Standard Deviation of the group's total wound volume at day one and last treatment day. Wound volume was measured as Length x Width X Depth (when able to determine depth). This is to assess the change in volume, in order to assess wound progress towards closure.
Time Frame
Initial measurement at day 1 and measurement at the subject's last visit at 12 weeks or sooner if the wound closed before then.
Title
Wounds With Slough/Eschar Reduction on Visit 2 and Wounds With Slough/Eschar Reduction at Last Visit
Description
Mean and Standard Deviation of the group's percent adherent and/or non-adherent slough present in the wound bed at day one and last treatment day. This is to assess the change in slough/eschar. This is to determine progression from contact to noncontact ultrasound therapy, as well as to determine progress of wound bed quality.
Time Frame
Day 2 and measurement at the subject's last visit at 12 weeks or sooner if the wound closed before then.
Other Pre-specified Outcome Measures:
Title
Wounds With Granulation Present on Visit 1 and Wounds With Granulation Present at Last Visit
Description
Mean and Standard Deviation of the group's total percent of granulation tissue present in the wound bed at day one and last treatment day. This is to assess the change in granulation, in order to assess progress of wound bed quality.
Time Frame
Initial measurement at day 1 and measurement at the subject's last visit at 12 weeks or sooner if the wound closed before then.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is referred to Physical Therapy for contact ultrasound (which is included in the VIP protocol); Lower extremity (including foot) wound(s) of any etiology; Wound(s) presenting with slough, necrotic tissue, and/or non-viable tissue requiring debridement; Wound is present for 4 weeks or longer at the start of ultrasonic therapy; Insurance approval is obtained for Contact and Noncontact ultrasound treatments, in the ambulatory setting; Patient is 18 years of age or older; Female patient attesting not to be pregnant; Not undergoing Vacuum Assisted Closure (VAC) therapy. Exclusion Criteria: Patient is referred to Physical Therapy for noncontact ultrasound only; Wound(s) not on lower extremity; Clean wound(s) that do not require debridement; Wound onset less than 4 weeks prior to the start of ultrasonic therapy; Malignancies on the treatment area; Patients in the ambulatory setting whose insurance did not approve them for both contact and noncontact ultrasound therapy; Patient is under 18 years of age; Female patient attesting to be pregnant; VAC Therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisley Viana, PTMS
Organizational Affiliation
Texas Health Resources - Presbyterian Hospital of Dallas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Texas Health Resources - Presbyterian Hospital of Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75231
Country
United States

12. IPD Sharing Statement

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Healing Rate of Leg Wounds Treated With Contact and Noncontact Ultrasound: The VIP Ultrasound Protocol

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