High Ankle Block Versus Regional Block for Acute Pain Control After Ankle Surgery
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Jacksonville, Florida: 18-002398
NCT ID: NCT03894098
Sponsor Protocol Number: 18-002398
About this study
The purpose of this study is to assess high ankle block versus regional block for acute pain control after ankle surgery.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:
- Patients undergoing ankle surgery
- Age 18 and older who agree to enroll
Exclusion Criteria:
- Neurologic disorders such as peripheral neuropathy, complex regional pain syndrome, neurologic surgery, narcotic dependency, and anyone unable to receive an ankle block.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Jacksonville, Fla.
Mayo Clinic principal investigator Glenn Shi, M.D. |
Closed for enrollment |
|
More information
Publications
Publications are currently not available