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 @ 1:29 PM
Ignite Modification Date:
2025-12-24 @ 1:29 PM
NCT ID:
NCT02195895
Eligibility Criteria:
Inclusion Criteria:
* Prior enrollment in protocol "Effect of Teriparatide, Vibration and the Combination on Bone Mass and Bone Architecture in Chronic Spinal Cord Injury", (NCT01225055).
* Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy.
* Ability to understand and the willingness to sign a written informed consent.
Exclusion Criteria:
* Individual with renal insufficiency (calculated creatinine clearance \< 30 ml/min).
* Individuals who are not able to sit or stand upright for at least 30 minutes after taking their medication.
* Individuals with poor dental hygiene.
* Individuals with esophageal abnormalities.
* Individuals who are not able to tolerate alendronate treatment.
* Individuals who will not be able to return for all study visits.
* Patients may not be receiving any other investigational agents.
* Other medical conditions that in the opinion of the investigator would preclude the subject from completing the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
21 Years
Study:
NCT02195895
Study Brief:
Protocol Section:
NCT02195895