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 @ 3:57 PM
Ignite Modification Date:
2025-12-24 @ 3:57 PM
NCT ID:
NCT05459792
Eligibility Criteria:
Inclusion Criteria:
1. Gender both males and females
2. ASA Class II
3. Age 18-70 years
4. Patients undergoing surgeries requiring radial arterial cannulation expected to be needed , and in place for the first 24 hours postoperatively as thoracic surgeries(e,g lobectomy, pneumonectomy),major vascular surgeries (carotid end arterctomy,abdominal aneurysm) , or major abdominal surgery .
Exclusion Criteria:
1. Hypersensitivity or knownallergy to amide local anesthetics
2. Pre-existing neurological deficit/peripheral neuropathy and Coagulation disorders.
3. Local infection at the site of block and at the planned cannulation site.
4. peripheral occlusive vascular disease, surgery for vascular injury or thromboembolic phenomena, cervical rib, and conditions associated with obstruction to arterial or venous flow.
5. Emergency operations and occlusion of the ipsilateral ulnar artery
6. patients on vasopressors and radial artery cannula removal before 24 hours postoperative.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT05459792
Study Brief:
Protocol Section:
NCT05459792