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Clinical Trials/NCT01501500
NCT01501500
Completed
Phase 4

Therapeutic Effect of Botulinum Toxin Type A in Addition to Total Contact Insole in Treating Painful Hallux valgus-a Pilot Study

Chang Gung Memorial Hospital1 site in 1 country25 target enrollmentAugust 2010

Overview

Phase
Phase 4
Intervention
BOTOX
Conditions
Hallux Valgus
Sponsor
Chang Gung Memorial Hospital
Enrollment
25
Locations
1
Primary Endpoint
hallux valgus angle
Status
Completed
Last Updated
12 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
August 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Chang Gung Memorial Hospital
Responsible Party
Sponsor

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

Arms & Interventions

botulinum toxin type A. HV angle

intramuscular injection of BTA into target muscle

Intervention: BOTOX

Normal saline, HV angle

intramuscular injection of normal saline into target muscle

Intervention: Normal Saline (0.9% NaCl)

Outcomes

Primary Outcomes

hallux valgus angle

Time Frame: up to 18 months

radiological assessment before and after the intervention

Secondary Outcomes

  • foot function index for quality of life(up to 18 months)

Study Sites (1)

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