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Effect of Botulinum Toxin to Hallux Valgus in Addition to Total Contact Insole

Primary Purpose

Hallux Valgus

Status
Completed
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
BOTOX
Normal Saline (0.9% NaCl)
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hallux Valgus focused on measuring botulinum toxin type A, hallux valgus angle, foot function index, VAS pain scale

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • hallux valgus with angle of at least 20°,
  • single or bilateral hallux valgus.

Exclusion Criteria:

  • history of foot operations,
  • rheumatoid arthritis and gouty arthritis.
  • Any contraindication on BTA administration

Sites / Locations

  • Chang Gung MH

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

botulinum toxin type A. HV angle

Normal saline, HV angle

Arm Description

intramuscular injection of BTA into target muscle

intramuscular injection of normal saline into target muscle

Outcomes

Primary Outcome Measures

hallux valgus angle
radiological assessment before and after the intervention

Secondary Outcome Measures

foot function index for quality of life
Foot Function Index before and after the intervention

Full Information

First Posted
December 21, 2011
Last Updated
September 5, 2013
Sponsor
Chang Gung Memorial Hospital
Collaborators
National Science Council, Taiwan
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1. Study Identification

Unique Protocol Identification Number
NCT01501500
Brief Title
Effect of Botulinum Toxin to Hallux Valgus in Addition to Total Contact Insole
Official Title
Therapeutic Effect of Botulinum Toxin Type A in Addition to Total Contact Insole in Treating Painful Hallux valgus-a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
August 2010 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital
Collaborators
National Science Council, Taiwan

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators propose a new therapeutic approach by injecting Botulinum Toxin Type A (BTA) to the oblique and transverse heads of adductor muscle of the great toe. BTA works by binding presynaptically to high-affinity recognition sites on the cholinergic nerve terminals and decrease the release of acetylcholine, causing a neuromuscular blocking effect. The investigators hypothesize that BTA injection may help to decrease the hallux valgus angle by decrease adductor hallucis muscle activation. Thereby enhance the therapeutic result of hallux valgus treated with total contact insole. The outcome measurement may shed light in treating patient with painful hallux valgus and document evidence for plantar pressure changes in acute, sub-acute and chronic stage.
Detailed Description
This is a randomized, double-blind, placebo-controlled prospective study to assess the influence and efficacy of intramuscular (IM) Botulinum Toxin Type A (BTA) injection in patients with painful hallux valgus with the use of total contact insole. Fifty feet with painful hallux valgus will be collected. Informed consent is obtained according to the hospital's medical ethics and the human clinical trial committee. The feet will be randomized into 2 groups: Group A (n=25, treatment group) and Group B (n=25, control group). Clinical diagnosis of hallux valgus is made based on observation of great toe lateral deviation. Inclusion criteria were hallux valgus with angle of at least 20°, single or bilateral hallux valgus. To obtain the hallux valgus angle, foot roentgenography in AP and sesamoid views under the weight bearing condition will be obtained. The angle formed by lines drawn to bisect the first metatarsal bone and the proximal phalanx of the great toe will be measured. The exclusion criteria include history of foot operations, rheumatoid and gouty arthritis, and any contraindication to BTA administration. Subjective data such as the Foot Function Index will be collected.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hallux Valgus
Keywords
botulinum toxin type A, hallux valgus angle, foot function index, VAS pain scale

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
botulinum toxin type A. HV angle
Arm Type
Active Comparator
Arm Description
intramuscular injection of BTA into target muscle
Arm Title
Normal saline, HV angle
Arm Type
Placebo Comparator
Arm Description
intramuscular injection of normal saline into target muscle
Intervention Type
Drug
Intervention Name(s)
BOTOX
Other Intervention Name(s)
BOTOX (Allergan, Irvine, CA)
Intervention Description
once injection of BTA 3oU into hallux oblique and transverse heads each
Intervention Type
Drug
Intervention Name(s)
Normal Saline (0.9% NaCl)
Intervention Description
Normal saline 0.3ml to oblique and transverse heads each
Primary Outcome Measure Information:
Title
hallux valgus angle
Description
radiological assessment before and after the intervention
Time Frame
up to 18 months
Secondary Outcome Measure Information:
Title
foot function index for quality of life
Description
Foot Function Index before and after the intervention
Time Frame
up to 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: hallux valgus with angle of at least 20°, single or bilateral hallux valgus. Exclusion Criteria: history of foot operations, rheumatoid arthritis and gouty arthritis. Any contraindication on BTA administration
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katie P Wu, MD
Organizational Affiliation
Chang Gung Memorial Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chang Gung MH
City
Gueishan
State/Province
Taoyuan
ZIP/Postal Code
333
Country
Taiwan

12. IPD Sharing Statement

Citations:
PubMed Identifier
25683315
Citation
Wu KP, Chen CK, Lin SC, Pei YC, Lin RH, Tsai WC, Fuk-Tan Tang S. Botulinum Toxin type A injections for patients with painful hallux valgus: a double-blind, randomized controlled study. Clin Neurol Neurosurg. 2015 Feb;129 Suppl 1:S58-62. doi: 10.1016/S0303-8467(15)30014-7.
Results Reference
derived

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Effect of Botulinum Toxin to Hallux Valgus in Addition to Total Contact Insole

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