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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03133039
Other study ID # R16143
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2015
Est. completion date December 1, 2021

Study information

Verified date August 2019
Source Tampere University Hospital
Contact Nkke Partio, M.D
Phone +3583 311611
Email partio.nikke.n@student.uta.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators sought to determine whether bioabsorbable cannulated screws could perform as well as titanium cannulated screws in the Lapidus procedure and MTP1-joint arthorodesis in anatomical models and clinical series of the foot.


Recruitment information / eligibility

Status Recruiting
Enrollment 2
Est. completion date December 1, 2021
Est. primary completion date December 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- valuntary 18-65-yers-old, patient have hallux valgus or hallux rigidus deformity which need surgery treatment

Exclusion Criteria:

- Over 65 yers-old or less than 18-years-old, diabetes, rheumatism, smoker or lack of co-operation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
surgery, bioabsorbable screw
In this study we compare bioabsorbable and titanium screw in the hallux valgus and hallux rigidus surgery

Locations

Country Name City State
Finland Faculty of Medicine Tampere Pirkanmaa

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary AOFAS score score 2 years
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