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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04088214
Other study ID # NTEC-2019-0340
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date May 1, 2019

Study information

Verified date September 2019
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Lateral soft tissue release is commonly performed as part of the surgical correction of hallux valgus. This study will look at the results form a series of patients whom have underwent the arthroscopic lateral soft tissue release.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date May 1, 2019
Est. primary completion date April 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion:

- >18 and legally fit for consent

- Symptomatic hallux valgus with HVA >15 degrees

Exclusion:

- Active physical or mental disorders that could affect rehabilitation including

- Other conditions affecting ambulation: lower limb injury, neuromuscular problems etc.

- Mental incapacitation

- Previous hallux valgus surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Arthroscopic lateral soft tissue release
The arthroscopic lateral soft tissue release is performed using an inside-out approach via the 1MTPJ arthroscopy.

Locations

Country Name City State
Hong Kong CUHK Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary HVA • Hallux valgus angle (HVA) measured on a weight-bearing DP radiograph 12 weeks post-surgery
Primary HVA • Hallux valgus angle (HVA) measured on a weight-bearing DP radiograph 52 weeks post-surgery
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