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NCT05165134 Clinical Trial

Hallux Valgus Conservative Treatment

Hallux Valgus Clinical Trial

— RCT  

Official title:
Influence of Short-Term Conservative Treatment Using Kinesiotape on Hallux Valgus Angle

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05165134
Other study ID # JU
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 24, 2020
Est. completion date November 15, 2021

Study information
Verified date December 2021
Source University of Jazan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Studying the effect of kinesiotape on hallux valgus angle and pain in hallux valgus patients.

Description:

30 patients (male and female) suffering from bilateral Halux valgus. Divided randomly into 2 groups 1. st group receive kinesiotape bilaterally for correction : Hallux valgus angle (HVA) was measured using Xray and pain was measured using VAS before applying tape and after 8 weeks of tape application. 2. nd group receive placebo tape bilaterally and had the same measurements. 2 groups were on a group of exercises

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date November 15, 2021
Est. primary completion date January 29, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - mobile hallux valgus Exclusion Criteria: - using orthotics - knee malalignment

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Kinesiotape
Elastic tape used for mechanical correction of the deformity in study group and placebo in control group

Locations
Country Name City State
Saudi Arabia Jazan University Gizan Jazan

Sponsors (1)
Lead Sponsor Collaborator
University of Jazan

Country where clinical trial is conducted

Saudi Arabia, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hallux valgus angle (HVA ) Hallux valgus angle measured by x ray 8 weeks
Primary Pain on metatarsophalangeal joint measured by visual analogue scale (VAS) 8 weeks
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