Combination of Peripheral Nerve Block and DepoDur in Total Knee Joint Replacement

PHASE4TerminatedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

December 31, 2009

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2012

Conditions
Arthroplasty, Replacement, Knee
Interventions
DRUG

Depodur

7.5 mg Depodur via the epidural catheter

PROCEDURE

sciatic nerve block

The sciatic nerve will be identified at the subgluteal level with ultrasound. A point 3 cm lateral and 4 cm caudad will be marked. Patients will be placed in the lateral position. A 18 G Tuohy needle will be inserted at a 45° angle until a peroneal or tibial twitch is obtained at 1.5 mA. Once the current can be reduced to obtain a twitch less than 0.5 mA, a catheter will be inserted and placed perineurally. If placed preoperatively, the catheter will be flushed with normal saline or 5% dextrose and will not be dosed until after surgery. After the patient is in the PACU and the surgeons have verified the sciatic nerve function, the sciatic catheter will be dosed with 35 mL 0.25% ropivacaine.

Trial Locations (1)

40202

University of Louisville Hospital, Louisville

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

EKR Therapeutics, Inc

INDUSTRY

lead

University of Louisville

OTHER

NCT00895531 - Combination of Peripheral Nerve Block and DepoDur in Total Knee Joint Replacement | Biotech Hunter | Biotech Hunter