Continuous Lumbar Plexus Block With and Without Parasacral Block in Patients Undergoing Total Hip… (NCT02161484) | Clinical Trial Compass
TerminatedNot Applicable
Continuous Lumbar Plexus Block With and Without Parasacral Block in Patients Undergoing Total Hip Replacement
Stopped: The computer is crushed and all data is lost (IT was not able to recover it. Last data was collected 6.17.14)
United States10 participantsStarted 2014-01
Plain-language summary
The purpose of this research study is to evaluate the analgesic efficacy of adding a single shot parasacral (sciatic) nerve block to a continuous lumbar plexus block in patients undergoing total hip replacement.
Who can participate
Age range18 Years – 75 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Subject has signed and dated an Informed Consent Form.
✓. Subject is classified as a ASA (American Society of Anesthesiologists) status I-III
✓. Subject is age 18- 75 years old.
✓. Subject is having primary total hip arthroplasty
✓. No contraindication to peripheral nerve catheter ( local infection or hypocoagulable state)
✓. Patient willing to receive spinal anesthesia as operative anesthesia
✓. No known drug allergies to study medications
✓. Patients not expected to receive therapeutic anticoagulation in the postoperative period.
Exclusion criteria
✕. Subject inability to provide adequate informed consent.
✕. Age younger than 18 years or older than 75 years
✕. Any contraindication to the placement of lumbar plexus catheter, including local infection, hypocoagulable state.
✕. ASA (American Society of Anesthesiologists) physical status of IV or greater