Off- Loading Shoe to Improve Healing and Prevention of Recurrence of Neuropathic Diabetic Plantar Foot Ulcers (SANIBA)
Primary Purpose
Diabetes Mellitus, Diabetic Neuropathic Foot Ulcer
Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
SANIDIAB
BAROUK
Sponsored by
About this trial
This is an interventional treatment trial for Diabetes Mellitus focused on measuring Diabetic foot ulcer, Off loading, Compliance, Healing duration, Amputation rate
Eligibility Criteria
Inclusion criteria :
- More of 18 years old man or woman
- Type 1 or 2 Diabetes mellitus
- A new plantar ulcer of the fore foot or the toes
- GRADE 1A or 2 A of the University of Texas Classification
- Neuropathy assessed by absence of sensation in 10g monofilament test
Exclusion criteria
- Severe angiopathy (Grade 3 of the PEDIS classification)
- Osteomyelitis or cellulitis of the foot
- Transmetatarsal amputation
- Other study in course
- Immunosuppressive drugs, antibiotic therapy,
- Hepatic insufficiency
- No possibility to follow the patients every 14 days
- No state health insurance
- Pregnancy
Sites / Locations
- Groupe hospitalier Pitié-Salpêtrière
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
barouk
sanidiab
Arm Description
Outcomes
Primary Outcome Measures
Healing duration of the diabetic foot ulcer
Secondary Outcome Measures
Rate of reulceration
Rate of amputation
Compliance of patients to footwear
Full Information
NCT ID
NCT01586481
First Posted
April 25, 2012
Last Updated
November 13, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
MAYZAUD
1. Study Identification
Unique Protocol Identification Number
NCT01586481
Brief Title
Off- Loading Shoe to Improve Healing and Prevention of Recurrence of Neuropathic Diabetic Plantar Foot Ulcers
Acronym
SANIBA
Official Title
Effectiveness and Safety of an Off- Loading Shoe to Improve Healing and Prevention of Recurrence of Neuropathic Diabetic Plantar Foot Ulcers of the Fore Foot: a Prospective Randomised Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
February 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
MAYZAUD
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
It's a pilot prospective opened multicentric randomised study. We measure the efficiency and the safety of a new concept of off-loading shoe (SANIDIAB) compared with an old one (BAROUK) to treat chronic diabetic foot ulcer which involved a high risks of amputation 64 diabetic patients with a plantar neuropathic ulcer of the fore foot without infection, osteomyelitis or angiopathy, will be included. 32 patients will be treated with SANIDIAB shoe and 32 with BAROUK shoe
Detailed Description
Name of the study : SANIBA
Objective:
The gold standard to heal diabetic foot ulcers is complete off-loading. To wear continuously off loading shoe is very difficult The bad compliance of the patients can lead to infection of the ulcer and amputation of the foot.
The purpose of this study is to compare the efficacy of a new concept of off-loading shoe (a pair of SANIDIAB shoes) with a single BAROUK shoe to treat chronic plantar diabetic foot ulcer of the fore foot. The hypothesis is that the new concept is more efficient because of a good off-loading associated with a best compliance to wear the new concept of shoes.
The study will last 18 months with a duration of study of 6 months per patient It's a pilot prospective multicenter randomised study of 64 diabetic patients with a plantar neuropathic ulcer of the fore foot, treated after randomisation by an off loading shoe BAROUK or a pair of off loading shoes SANIDIAB.
Patients will be followed in a diabetic foot department every 14 days until healing and after healing until 6 months after inclusion in the study.
The main outcome measure is the healing duration of the diabetic foot ulcers in both group of treatment.
The secondary outcome measure is the rate of reulceration after healing , the rate of amputation and compliance of patients 64 patients will be included in 2 groups: 32 will wear SANIDIAB shoes and 32 BAROUK shoe.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Diabetic Neuropathic Foot Ulcer
Keywords
Diabetic foot ulcer, Off loading, Compliance, Healing duration, Amputation rate
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
barouk
Arm Type
Active Comparator
Arm Title
sanidiab
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
SANIDIAB
Intervention Description
off-loading shoe
Intervention Type
Device
Intervention Name(s)
BAROUK
Intervention Description
old shoe
Primary Outcome Measure Information:
Title
Healing duration of the diabetic foot ulcer
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Rate of reulceration
Time Frame
6 months
Title
Rate of amputation
Time Frame
6 months
Title
Compliance of patients to footwear
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria :
More of 18 years old man or woman
Type 1 or 2 Diabetes mellitus
A new plantar ulcer of the fore foot or the toes
GRADE 1A or 2 A of the University of Texas Classification
Neuropathy assessed by absence of sensation in 10g monofilament test
Exclusion criteria
Severe angiopathy (Grade 3 of the PEDIS classification)
Osteomyelitis or cellulitis of the foot
Transmetatarsal amputation
Other study in course
Immunosuppressive drugs, antibiotic therapy,
Hepatic insufficiency
No possibility to follow the patients every 14 days
No state health insurance
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Georges HA VAN, MD
Organizational Affiliation
APHP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Groupe hospitalier Pitié-Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France
12. IPD Sharing Statement
Learn more about this trial
Off- Loading Shoe to Improve Healing and Prevention of Recurrence of Neuropathic Diabetic Plantar Foot Ulcers
We'll reach out to this number within 24 hrs