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:
2025-12-24 @ 2:14 PM
Ignite Modification Date:
2025-12-24 @ 2:14 PM
NCT ID:
NCT06795295
Eligibility Criteria:
Inclusion Criteria:
* Free from any systemic disease.
* Free from any medical or surgical conditions that cause dysphagia (swallowing problems).
* A sufficient residual alveolar bone quantity (height and width). This was verified by a CT scan using cone-beam computed tomography for each patient.
* All patients had sufficient bone either D2 or D3 by measuring the Hounsfield unit on CBCT scan.
* Residual ridges are covered by firm healthy mucosa.
* Class I maxilla-mandibular relationship.
* sufficient inter-arch space and restorative space for locator retained mandibular overdenture.
Exclusion Criteria:
* Patient with absolute contraindications for implant placement such as active cancer, immunosuppression, bleeding issues, and metabolic diseases that directly affect the bone such as osteoporosis, and hyperparathyroidism.
* Patients with relative contraindication: history of para functional habits such as bruxism, clenching, and bad habits such as smoking and alcoholism, uncontrolled diabetic patients.
* Patients with local contraindications for implant placement due to localized bone defects.
* Non-cooperative patients who don't follow instructions during and after the operation.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
45 Years
Maximum Age:
70 Years
Study:
NCT06795295
Study Brief:
Protocol Section:
NCT06795295