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 @ 7:45 PM
Ignite Modification Date:
2025-12-24 @ 7:45 PM
NCT ID:
NCT02058303
Eligibility Criteria:
Inclusion Criteria:
* patients 18 years or older having hand, wrist, or finger surgery
* ability to understand and provide informed consent
* American Society of Anesthesiologists status I-III
* presence of a responsible adult caregiver for 48-72 hours after surgery
Exclusion Criteria:
* patient refusal or inability to provide informed consent
* true allergy, not sensitivity to local anesthetics, midazolam, fentanyl, hydromorphone, propofol
* pregnancy
* hepatic or renal failure
* evidence of infection at or near the proposed needle insertion site
* any sensorimotor deficit of the upper extremity
* BMI greater than or equal to 35
* uncontrolled or severe pulmonary disease
* anticoagulant use (not aspirin or non-steroidal anti-inflammatories)
* chronic pain patients
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02058303
Study Brief:
Protocol Section:
NCT02058303