BION Active Seating for Pressure Ulcer Prevention

Pressure Ulcer Clinical Trial

Official title:

BION Active Seating for Pressure Ulcer Prevention

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00628602
• Other study ID #: BT8
• Status: Completed
• Phase: Phase 1
• First received: February 25, 2008
• Last updated: June 1, 2015
• Start date: November 2007
• Est. completion date: December 2008

Study information

• Verified date: June 2015
• Source: University of Southern California
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Pressure ulcers (PUs) are a debilitating pathology resulting from pressure and shear in the soft tissues of immobilized patients. In studies to date, BION neuromuscular stimulation has been demonstrated to activate strong muscle contractions and to produce skeletal motion, with associated increases in muscle bulk (hypertrophy), strength, and metabolic capacity, hence counteracting the 3 major etiological factors in PU development (immobility, soft-tissue atrophy and hypoxia).

This study intends to use neuromuscular stimulation to both shift paralyzed subjects' weight and build up gluteal muscle volume, in order to prevent recurrence of pressure ulcers. We will implant BIONs alongside the already exposed inferior gluteal and sciatic nerves in patients who are undergoing gluteal rotation flap surgery for PU reconstruction. The gluteal rotation flap is a common reconstructive technique for treating PUs by bringing healthy muscle and skin in to repair the deficient area, and to provide healthy tissue covering over bony prominences. The implanted BIONs will enable us subsequently to stimulate the gluteus maximus and hip extensor muscles. Outcome measures will include tissue health variables (measured by clinical assessment, X-Rays, MRI and Sesta-MIBI SPECT perfusion scans), pressure redistribution (measured by an array of pressure sensors), and recurrence rates over 12 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3
• Est. completion date: December 2008
• Est. primary completion date: December 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Subject has had a spinal cord injury and has bilateral lower limb paralysis.

2. Subject cannot contract his/her gluteus muscle voluntarily.

3. Subject is between 18 and 70 years old.

4. Subject sits in a wheelchair for at least 5 hours per day.

5. Attending physician considers the subject in general good health (other than SCI and PU wound).

6. Subject has one or more PUs of Stage III or IV (according to National Pressure Ulcer Advisory Panel Staging1).

7. Subject is having a musculocutaneous (not cutaneous or fasciocutaneous) gluteal rotation flap surgery for PU treatment in which the inferior gluteal pedicle and sciatic nerve will be exposed but not damaged or sacrificed in any way (for any PU wound(s)).

8. Subject is mentally capable of understanding the goals and the application of therapy.

9. Subject is able to apply the therapy (with or without help) once discharged from Rancho Los Amigos.

10. Subject is willing and capable of giving informed consent.

11. Subject is willing and capable of traveling to testing center at the schedules.

Exclusion Criteria:

1. Subject has a positive pregnancy test, is nursing / lactating, or is planning on becoming pregnant or is unwilling to not become pregnant in the next 12 months.

2. Subject has an electronic implant (e.g. cardiac pacemaker, etc.).

3. Subject has any condition associated with a wound healing abnormality (e.g.:

connective tissue disorder, immune disorder, diabetes, clinical obesity).

IDE application: BION Active Seating for Pressure Ulcer Prevention Page 65

4. Subject is malnourished.

5. The attending physician has concerns about the healing of this subject (e.g.: heavy smoking, excessive and/or poorly-managed incontinence).

6. Subject has concurrent concomitant condition affecting the buttock/pelvic area, including other pressure wound not corrected by the flap surgery.

7. Subject suffers from claustrophobia or fear of MRI, or has any contraindication to MRI (e.g. metal implants, pacemaker, etc. not suited to MRI).

8. Subject has damage to the inferior or superior gluteal neurovascular pedicles.

9. Subject is / plans to participate in another investigational study that may affect the healing of PUs or prevent their occurrence/recurrence.

10. Subject is using medications / undergoing procedures that will interfere with NMES effecting muscle contraction (e.g. treatments for spasticity and / or spasms, such as: neurotomies, tenotomies, myotomies, and rhizotomies; as well as tranquilizers and muscle relaxant / paralyzing agents such as Baclofen (Lioresal®), Dantrolene (Dantrium®) and Botulinum Toxin Type A (Botox®)).

11. Subjects whose ulcer extends more than 2.25" deep to the projected surface contour of the buttock when the patient is in a prone position (measured perpendicular to the base of the PU, from the deepest point of the PU to the level of the highest point of the buttock surface, when prone)

12. Subject's wheelchair and the BION system have been tested for interference of either with the other's operation, and either does not operate normally when used together, and this cannot be resolved with an available alternate wheelchair.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pressure Ulcer
• Ulcer

Intervention

Device:
• BION
30 patients operated will be randomized into 2 equal groups, a BION Therapy Group ("Rx group") and a Control Group ("Control group").

Locations

Country	Name	City	State
United States	Rancho Los Amigos National Rehabilitation Center	Downey	California

Sponsors (1)

Lead Sponsor	Collaborator
University of Southern California

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical assessment of movement and shifting of weight during BAS. Record shifts in pressure distribution over seated pressure points during NMES.		upon discharge and at the 12-week, 20-week, 36-week and 52-week outpatient follow-up visits.	No
Secondary	Clinical Examination of Braden Scale assessment,Reperfusion time,Recurrence of wounds and Body Mass Index		preoperation, upon removal of sutures, upon discharge, and at the 12-week, 20-week, 36-week and 52-week outpatient follow-up visits.	Yes