Comparison Between Postoperative Tubular Dressing and a Vacuum Removable Rigid Dressing After Transtibial Amputation

Edema Leg Clinical Trial

— EMPAR  

Official title:

Comparison of Wound Healing, Edema Level, Knee Range of Motion, Protection Post Falls, Device Application, Time to Prosthetic Fit, and Cost Between Postoperative Soft Dressing and Vacuum Removable Rigid Dressing After Transtibial Amputation

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03948087
• Other study ID #: EMPAR
• Status: Not yet recruiting
• Phase: N/A
• Start date: May 2019
• Est. completion date: May 2021

Study information

• Verified date: May 2019
• Source: Covenant Health
• Contact: Amputee Coordinator
• Phone: 780-735-7161
• Email: trent.duchscherer[@]covenanthealth.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Comparison of wound healing, edema level, knee range of motion, rate of revision post falls, device application time, time to prosthetic fit, and cost between postoperative soft dressing and a vacuum removable rigid dressing after unilateral transtibial amputation.

Description:

The gold standard after transtibial amputation is casting of the residual limb to limit room for post-surgical edema, enable faster wound healing and shorter hospital stays, as well as, reduce time to prosthetic fitting. Casting also reduces the risk of impact damage to the limb. Casting, however, is costly and impractical due to the requirement of a prosthetist available on call for after emergency amputation surgeries and a need for multiple repeat prosthetist visits to cut off and reapply casting after wound healing checks. Thus current practice involves use of a compression elastic tube bandage (like a tensor bandage) applied within 15 minutes after surgery. However this bandage applies pressure to the residual limb, which can increase risk of reduced blood supply to the healing limb especially in vascular compromised patients. Further, this soft bandage does not offer any protection to the residual limb, a fall or severe contusion could lead to a requirement for costly revision surgery. There is evidence that rigid removable dressings can improve wound healing times, protect the limb, prevent contractures and enable earlier prosthetic fitting. This study aims to examine the the differences in wound healing time, changes in limb edema, knee range of motion, limb protection post falls, device application time, time to prosthetic fitting and cost between currently used postoperative soft dressing (SD) and vacuum removable rigid dressing (VRRD) after transtibial amputation.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: May 2021
• Est. primary completion date: October 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Transtibial amputation related to peripheral vascular disease with or without diabetes or trauma.

Justification: The form and function of the ORD device relates solely to transtibial amputees. The device is not useable for any other limb amputation type (e.g. transfemoral, transmetatarsal). The choice of using vascular compromised participants is intentional. Ischemia and necrosis rapidly ensue as a result of vessel occlusion which can easily happen with any external compressive force (e.g. tensor bandaging). The ORD does not apply compressive force to the residual limb.

2. Transtibial amputation that includes myodesis and/or myoplasty.

Justification: Myoplasty and myodesis are preferred surgical techniques while performing an amputation. They involve the surgical attachment of muscle to muscle (myoplasty) or muscle to bone (myodesis) across the end of the residual limb prior to skin flap closure. This allows increased stability and provides a better interface with a future prosthetic device.

3. Greater than 18 years of age

Justification: Below the age of 18 informed consent must be obtained by a parent or guardian

4. Patient must be able to speak and understand English in order to provide informed consent. No reliance on translator services will be implemented.

5. Has no major illness where life expectancy is less than 2 years.

Justification: This is the study timeline and co-morbidities that limit participation within this timeframe will introduce confounding factors.

Exclusion Criteria:

1. Severe dementia or insufficient cognition.

Justification: Inability to provide informed consent to participate in the study.

2. Knee contracture greater than 30 degrees

Justification: The ORD will not fit a limb with too much flexion at the knee. Wound healing is also affected due to pressure across the end of the residual limb without the use of offloading techniques.

3. Severe peripheral vascular disease involving the contralateral lower limb

Justification: Having severe peripheral vascular disease to the contralateral limb may affect the secondary outcome measures due to the need for further medical or surgical intervention.

4. Inability to speak, read, or understand English.

Justification: For a patient to participate in the study informed consent must be obtained. There is a high probability that there would be too much variability among translators (family member or institutional) to ensure consistent informed consent.

5. Neurological condition or medical disorder that could affect rehabilitation.

Justification: Rehabilitation post transtibial amputation is critical to overall functional outcomes as well as study outcomes. If a patient has difficulty with participation in rehabilitation then this will be a confounding factor.

Related Conditions & MeSH terms

• Amputation Stump
• Edema Leg
• Peripheral Arterial Disease
• Peripheral Vascular Disease With Complications
• Peripheral Vascular Diseases
• Vascular Diseases
• Wound Healing Delayed

Intervention

Device:
• Vacuum Removable Rigid Dressing (VRRD)
Intra-operative application of device.

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Covenant Health	Alberta Innovates Health Solutions

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluation of Change in Stump Wound Healing	The Photographic Wound Assessment Tool (PWAT) will be used in a blinded fashion to evaluate the level of change in wound healing of the transtibial amputation primary closure. The PWAT incorporates type and amount of necrotic tissue, wound edge definition, surrounding skin color, epithelialization, and granulation of tissue. A score of 0/24 on the PWAT indicates complete wound closure.	Day 3,7,14,30,48
Secondary	Evaluation of Change in Level of Limb Edema	Circumferential measurements will be taken at two levels of the residual stump. Centimeters measured circumferentially at 5 cm from the distal end and around the knee at the center of the patella	Day 3,7,14,30,48
Secondary	Evaluation of Change in Knee Range of Motion	Degrees measured via goniometry into knee flexion and extension for both active and passive range of motion.	Day 3,7,14,30,48
Secondary	Rate of Revision Post Falls	Falls sustained by study participants will be recorded. Whether a follow-up revision surgery was necessary will also be recorded.	Until prosthetic limb fit, on average 2 months.
Secondary	Total Amount of Time to Apply, Change, Clean and Alter the Dressings	Time log in minutes recorded by staff in real time providing care to study participants.	Until discharge from acute care, on average 2 weeks.
Secondary	Length of time Until the Residual Limb is Ready for Prosthetic Fitting	Time log in days beginning post operative day 1 until the study participant is fit with a definitive prosthetic limb.	Through study completion, on average 2 months.
Secondary	Total Length of Stay in Acute and Sub-acute Care Facilities	A time log in days of how long a given study participant is admitted to an acute or sub-acute care facility.	Through study completion, on average 3 weeks.