Actively Recruiting
Reversal of Spinal Anesthesia Residual Motor Block Via Intrathecal Catheter
Led by Beth Israel Deaconess Medical Center · Updated on 2026-04-20
20
Participants Needed
1
Research Sites
88 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to determine the feasibility of administering a predetermined amount of normal saline into the intrathecal or subarachnoid space via a small spinal catheter to reduce or eliminate the effects of previously injected spinal anesthetic following lower extremity orthopedic surgery.
CONDITIONS
Official Title
Reversal of Spinal Anesthesia Residual Motor Block Via Intrathecal Catheter
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients having elective lower extremity joint replacement surgery
- Patients >18 years
You will not qualify if you...
- Contraindications to spinal anesthesia such as refusal, lumbar spinal hardware, or spinal abnormalities
- Patient on anticoagulation not withheld
- Patient receiving re-operation on the same joint
- Prior intra-cranial bleeding
- Patient's ASA status >3
- Non-English speaking
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
Research Team
A
Anna Fratello
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here