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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04628312
Other study ID # 2706201911419 C
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 20, 2020
Est. completion date December 2, 2020

Study information

Verified date November 2020
Source Mayuben Private Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this clinical trial is to check the effects of dry needling in the Flexor digitorum Brevis. Twenty healthy subjects wil be recruited for a quasi-experimental study. Participants will be from 18 to 40 years old, not obese. Participants will be measured before and after bilateral dry neddling in Flexor digitorum Brevis. The investigators will measure static footprint variables. The footprint variables will be divided in bilateral rear foot, bilateral midfoot, bilateral fore foot.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date December 2, 2020
Est. primary completion date November 27, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Flat foot grade II or II with - Must have latent trigger point in Flexor Brevis Digitorum muscles Exclusion Criteria: - Previous lower extremities surgery. - History of lower extremities injury with residual symptoms (pain, "giving-away" sensations) within the last year. - Leg-length discrepancy more than 1 cm

Study Design


Intervention

Other:
Static footprint
The static footprint will measure the plantar pressures and surface area of the back of the foot, midfoot and forefoot. Subjects were instructed to stand barefoot on the force platform, participants were instructed to remain in a relaxed standing posture with feet shoulder-width apart and positioned 30 degrees from the midline.

Locations

Country Name City State
Spain Mayuben Clinic San Sebastián De Los Reyes Madrid

Sponsors (1)

Lead Sponsor Collaborator
Mayuben Private Clinic

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variables of plantar pressures with platform before dry puncture During 30 seconds we will record the plantar pressure variables in grams per square centimeter. Through study completion, an average of 1 week
Primary Variable footprint plantar surface with platform before dry puncture For 30 seconds we will record the area of the footprint in square centimeters. Through study completion, an average of 1 week
Primary Variables of plantar pressures with platform after dry puncture During 30 seconds we will record the plantar pressure variables in grams per square centimeter. Through study completion, an average of 1 week
Primary Variable footprint plantar surface with platform after dry puncture For 30 seconds we will record the area of the footprint in square centimeters. Through study completion, an average of 1 week
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