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:
2025-12-25 @ 4:12 AM
Ignite Modification Date:
2025-12-25 @ 4:12 AM
NCT ID:
NCT06969820
Eligibility Criteria:
Inclusion Criteria:
* Age \> 39 years
* Typical clinical picture of plantar fasciitis for at least 3 months without associated trauma, other musculoskeletal co-morbidities or degenerative joint disease
* Patients with first-time application of LDRT to the affected joint
* Willingness to cooperate and accessibility of patients, especially geographical proximity, for treatment and follow-up
* Patients for whom LDRT is indicated independently of the study
* Karnofsky Index \>70%
Exclusion Criteria:
* Achillodynia ("dorsal" calcaneal spur)
* Previous trauma to the foot (fracture, tendon rupture)
* Musculoskeletal comorbidities of the foot
* Acute infections/open wounds in the area of the tendon to be examined or other relevant damage to the tendon to be examined
* Local steroid injections into the tendon prior to the study
* Rheumatic or vascular diseases, lymphedema
* Patients with tumors
* Individuals of childbearing potential who do not use adequate contraceptive measures consistently during therapy
* Persistent drug, medication or alcohol abuse
* Patients who have already undergone radiotherapy for the treatment of cancer
* Patients with an increased risk of an MRI examination, including the presence of metal implants, pacemakers or claustrophobia
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
40 Years
Study:
NCT06969820
Study Brief:
Protocol Section:
NCT06969820