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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02643485
Other study ID # 10111
Secondary ID
Status Recruiting
Phase N/A
First received December 29, 2015
Last updated January 30, 2017
Start date December 2015
Est. completion date September 2018

Study information

Verified date January 2017
Source Technische Universität München
Contact Norbert Harrasser, Dr.
Phone 0049 89 4140 5229
Email norbert.harrasser@gmx.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Static pedobarography is routinely used for pre- and postoperative questions regarding plantar foot pressure. This Investigation does insufficiently detect dynamic Forces. Hence, dynamic pedobarography might give some important insights in detecting plantar foot pressure after forefoot reconstruction.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 2018
Est. primary completion date July 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Forefoot surgery for hallux valgus or rigidus planned at out departement

Exclusion Criteria:

- No given consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Forefoot surgery
Forefoot surgery (Chevron, Scarf, Lapidus, Arthrodesis)

Locations

Country Name City State
Germany Klinikum rechts der Isar Munich Bavaria

Sponsors (1)

Lead Sponsor Collaborator
Technische Universität München

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary AOFAS-Score (American Orthopedic Foot and Ankle Society) 2 years
Secondary Plantar Peak Pressure Measuring will be performed by insole (Fa. Meticon) capable to detect plantar pressure in 80 regions of the sole of the foot 2 years