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Achilles Tendon Lengthening in Patients With Diabetes to Prevent Foot Ulcers

Primary Purpose

Diabetes Mellitus, Foot Ulcer, Peripheral Neuropathy

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Achilles tendon-lengthening surgery
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus focused on measuring Foot ulcers, Diabetes, Peripheral neuropathy, Casting, Achilles Lengthening, Ambulatory surgery, Foot deformity

Eligibility Criteria

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

Inclusion Criteria: History of Diabetes Mellitus Limitation of dorsiflexion ankle range of motion to zero degrees or less Recurrent or nonhealing ulcer (Grade II, Wagner scale) Exclusion Criteria: Nonambulatory patients or those that would not benefit from the Achilles lengthening procedure. Patients with a history of CVA or other significant neurological problems complicating their rehabilitation. Patients with a history of midfoot or hindfoot Charcot fractures. Patients with an Ankle-Arm index < 0.45 or absolute toe pressure < 40 mm Hg. Patients medically unfit for the anesthesia required for this Achilles lengthening procedure.

Sites / Locations

  • Barnes-Jewish Hospital, Orthopedic Surgery

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 1, 2000
Last Updated
June 23, 2005
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00006426
Brief Title
Achilles Tendon Lengthening in Patients With Diabetes to Prevent Foot Ulcers
Official Title
Controlled Clinical Trial Comparing the Effect of an Achilles Tendon Lengthening Procedure and Casting to Casting Alone for the Treatment of Neuropathic Forefoot Plantar Ulcers in Patients With Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
March 2003
Overall Recruitment Status
Completed
Study Start Date
August 1998 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2003 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

5. Study Description

Brief Summary
People with diabetes often develop severe skin problems (ulcers) on their feet. Sometimes these are treated with surgery and other times by temporarily immobilizing the foot in a cast. This study compares the effect of surgery to lengthen the Achilles tendon and put the foot in a cast, to using a cast alone. The study will also examine how foot strength, joint movement, and overall ability to walk, balance and climb stairs is affected.
Detailed Description
Patients with diabetes mellitus (DM) and peripheral neuropathy are at high risk for forefoot plantar ulcers and subsequent lower extremity amputation. Total contact casting currently is the most effective treatment for healing neuropathic plantar ulcers but ulcer recurrence is high (30-50%) when patients discontinue casting and resume walking. An equinus deformity (limited ankle dorsiflexion range-of-motion) is associated with these recurrent ulcers. Although descriptive evidence indicates an Achilles lengthening procedure (which corrects the equinus deformity) can improve healing rates in these chronic ulcers, there have been no controlled studies. This randomized prospective controlled clinical trial will determine if percutaneous Achilles lengthening and total contact casting is more effective than total contact casting alone in healing forefoot plantar ulcers (n=30/group will allow detection of 25% effect with power of 0.8 at alpha level of 0.05). Secondary purposes are to determine the effects of casting and percutaneous lengthening on measures of impairments, functional limitations, and disability in patients with DM and peripheral neuropathy. The specific aims of this project are to determine the effect of the Achilles lengthening procedure on patients with DM, peripheral neuropathy, a forefoot ulcer, and an equinus deformity in regards to 1) Wound healing, 2) Impairments (dorsiflexion range-of-motion, plantar flexor muscle performance), 3) Functional Limitations (Physical Performance Test, Functional Reach, walking ability), and 4) Disability (SF36). The results will have important implications for prevention of wound infection and lower extremity amputation; and improvement in impairments, functional limitations, and disability in this group of high risk patients with chronic disease. Approximately 30 patients will be recruited for each of the treatment groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Foot Ulcer, Peripheral Neuropathy
Keywords
Foot ulcers, Diabetes, Peripheral neuropathy, Casting, Achilles Lengthening, Ambulatory surgery, Foot deformity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Achilles tendon-lengthening surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: History of Diabetes Mellitus Limitation of dorsiflexion ankle range of motion to zero degrees or less Recurrent or nonhealing ulcer (Grade II, Wagner scale) Exclusion Criteria: Nonambulatory patients or those that would not benefit from the Achilles lengthening procedure. Patients with a history of CVA or other significant neurological problems complicating their rehabilitation. Patients with a history of midfoot or hindfoot Charcot fractures. Patients with an Ankle-Arm index < 0.45 or absolute toe pressure < 40 mm Hg. Patients medically unfit for the anesthesia required for this Achilles lengthening procedure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J. Mueller, Ph.D., P.T.
Organizational Affiliation
Program in Physical Therapy, Washington University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barnes-Jewish Hospital, Orthopedic Surgery
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
2659299
Citation
Mueller MJ, Diamond JE, Sinacore DR, Delitto A, Blair VP 3rd, Drury DA, Rose SJ. Total contact casting in treatment of diabetic plantar ulcers. Controlled clinical trial. Diabetes Care. 1989 Jun;12(6):384-8. doi: 10.2337/diacare.12.6.384.
Results Reference
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PubMed Identifier
12925622
Citation
Mueller MJ, Sinacore DR, Hastings MK, Strube MJ, Johnson JE. Effect of Achilles tendon lengthening on neuropathic plantar ulcers. A randomized clinical trial. J Bone Joint Surg Am. 2003 Aug;85(8):1436-45.
Results Reference
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PubMed Identifier
10693086
Citation
Hastings MK, Mueller MJ, Sinacore DR, Salsich GB, Engsberg JR, Johnson JE. Effects of a tendo-Achilles lengthening procedure on muscle function and gait characteristics in a patient with diabetes mellitus. J Orthop Sports Phys Ther. 2000 Feb;30(2):85-90. doi: 10.2519/jospt.2000.30.2.85.
Results Reference
background
Links:
URL
http://medschool.wustl.edu
Description
Washington University School of Medicine
URL
http://www.nichd.nih.gov/
Description
For more information on the National Institute of Child Health and Human Development (NICHD).

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Achilles Tendon Lengthening in Patients With Diabetes to Prevent Foot Ulcers

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