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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03594292
Other study ID # CMUH105-REC2-075
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 31, 2018
Est. completion date December 2019

Study information

Verified date January 2018
Source China Medical University Hospital
Contact Hsuan-Fang Ho
Phone 886-4-2296-7979
Email hlucy0630@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The FASTFORWARDTM Bunion Correction system has been cleared by the United States Food and Drug Administration for sale. This study is to investigate the clinical outcome of MedShape FASTFORWARDTM Bunion Correction system in treating hallux valgus patients at CMUH.

Criteria-There will be 12 subjects with a painful bunion and hallux valgus between 20 and 65 years of age and an adequate range of movement. Patients with rheumatoid arthritis, failed previous hallux valgus surgery and symptomatic and/or radiological arthritis of the MTP joint will be excluded.

Protocol-The PI and SC explain the detail and purpose of the project to the patient to the language to the patient is comfortable with. The explanation has to be at least 1 hour. Be sure the patients understand the full detail before the surgery.

Computer tomography scan, gait analysis and blood biochemical analysis will be taken in 1-2 weeks after patient is enrolled in the subject. Before surgery, the titration bone tether plate designed to match patent's second metatarsal contour will be manufactured using 3D printing technology. Printed titanium plate and PEEK screws used to secure tethering suture tape in the first metatarsal will be sterilized prior implantation. The surgery time, recovery period and effectiveness after implantation will be recorded. To observing the recovery situation, patients will back to out-patient clinic at 1st, 2nd, 3rd, 4th, 6th, 12th, 24th weeks. During these period, physical examination, wound dressing, VAS, X-ray scan will be arranged. The detail arrangements below:

1.1st week: physical examination, wound dressing, VAS

2.2nd week: physical examination, wound dressing, VAS

3.3rd week: physical examination, wound dressing, VAS, X-ray scan, remove stiches

4.4th week: physical examination, VAS

5.6th week: physical examination, VAS, X-ray scan

6.12th week: physical examination, VAS, X-ray scan

7.24th week: physical examination, VAS, X-ray scan, CT scan, gait analysis


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date December 2019
Est. primary completion date February 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients with a painful bunion and hallux valgus between 20 and 65 years of age and an adequate range of movement

Exclusion Criteria:

- Patients with rheumatoid arthritis, failed previous hallux valgus surgery and symptomatic and/or radio-logical arthritis of the MTP joint

Study Design


Related Conditions & MeSH terms


Intervention

Device:
FASTFORWARDTM Bunion
The participants will be assign to implantation of FASTFORWARDTM Bunion correction system surgery as a experimental group.
Procedure:
Conventional surgery
The participants will assign to conventional surgery as a control group, the procedure is a standard treatment for the 1st metatarsal hallux valgus.

Locations

Country Name City State
Taiwan China Medical University Hospital Taichung Beitun District

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intermetatarsal 1-2 angle postoperative Evaluating the angle among the 1st and the 2nd metatarsal assess by X-ray scan and CT scan 6 month
Secondary Assessment Foot Pressure Foot pressure assess by gait analysis 6 month
Secondary Pain using a visual analog scale Evaluating pain level by using visual analog scale 6 month
Secondary Intermetatarsal 1-2 angle Evaluating the angle among the first metatarsal and the first phalanx assess by X-ray scan 6 month
See also
  Status Clinical Trial Phase
Recruiting NCT03575338 - Minimally Invasive Versus Open Scarf Osteotomy for Hallux Valgus Correction: a Randomized Controlled Trial N/A
Completed NCT03504462 - Feasibility of Specific Anesthesia of the Forefoot Preserving the Sensitivity of the Heel for Foot Surgery N/A