Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:20 PM
Ignite Modification Date:
2026-03-26 @ 3:20 PM
NCT ID:
NCT07483320
Eligibility Criteria:
Inclusion Criteria:
* Age 18-65 years
* Diagnosis of unilateral midportion Achilles tendinopathy
* Symptoms present for more than 3 months
* VISA-A score \<80 at baseline
* Pre-injury physical activity level ≥3 on the Physical Activity Scale
* Ability to participate in rehabilitation program
Exclusion Criteria:
* Symptoms present for less than 3 months
* Prior PRP injection or ESWT treatment to the Achilles tendon within 3 months
* Other lower extremity musculoskeletal injury affecting function
* Symptomatic arthritis affecting the ankle or foot
* Rheumatologic disease or connective tissue disorder
* Coagulopathy or anticoagulant therapy affecting platelet function
* Neuropathy affecting pain perception
* Known cardiac condition contraindicating treatment
* Poorly controlled diabetes (HbA1c \>9.0)
* Pregnancy
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT07483320
Study Brief:
Protocol Section:
NCT07483320