Reversal of Spinal Anesthesia Residual Motor Block Via Intrathecal Catheter
Recruiting now · Phase 2
Conditions studied: Joint Replacement Surgery
In brief
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.
Key facts
- Study ID
- NCT07404982
- Run by
- Beth Israel Deaconess Medical Center
- People needed
- 24
- Starts
- 2026-03-19
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-07-31
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients having elective lower extremity joint replacement surgery
- Patients >18 years
You may not qualify if…
- Contraindications to spinal anesthesia (refusal, lumbar spinal hardware, 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
- Bromage score of 6 at the time of first PACU assessment post-enrollment
Where it is running
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States (enrolling)
Full record on ClinicalTrials.gov
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