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 @ 2:33 AM
Ignite Modification Date:
2025-12-25 @ 2:33 AM
NCT ID:
NCT06888934
Eligibility Criteria:
Inclusion Criteria:
* Patient requiring treatment of arthritis and/or correction of bone alignement defaultin the toes (mallet toes, claw toes, hammer toes),
* Use of the Lync® intramedullary osteosynthesis implantable medical device,
* No associated surgical procedures except:▪Flexor release/tenotomy
* MTP Arthrolysis / Extensor Lengthening
* Tendon transfers
* Phalangeal osteotomy
* Adult patient,
* Patient capable of respecting the prescriptions and recommendations of his surgeon,
* Patient able to read and understand the information note and the consent form,
* Patient able to sign a consent form.
Exclusion Criteria:
* Patient presenting a contraindication to the device under investigation;
* Simultaneous participation in another clinical investigation protocol;
* Adults subject to legal protection (judicial protection, curatorship, guardianship),persons deprived of their liberty, pregnant or breastfeeding women, minors
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06888934
Study Brief:
Protocol Section:
NCT06888934