Loss of Resistance, w/wo Stimulation, For Epidural Placement
Completed · Phase 4
Conditions studied: Anesthesia
In brief
The purpose of this randomized, observer-blinded, investigative trial is to determine if the use of electrical stimulation, compared to the traditional loss of resistance technique alone, improves the success rate of epidural catheter placement at an academic teaching institution.
Key facts
- Study ID
- NCT03087604
- Run by
- Wake Forest University Health Sciences
- People needed
- 100
- Starts
- 2017-03-17
- Expected to finish
- 2017-10-11
- Last updated by the study team
- 2020-06-17
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults undergoing intra-thoracic or intra-abdominal procedures that normally would receive thoracic epidurals for post-operative analgesia will be eligible.
You may not qualify if…
- Subjects with contraindications to regional anesthesia:
- history of allergy to amide local anesthetics
- presence of a progressive neurological deficit
- patients that are on anticoagulant medications that prohibit placement of an epidural
- Systemic infection
- Infection at the site of placement
Where it is running
- WakeForestUBMC — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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