Clinical Trials Directory

Trials / Terminated

TerminatedNCT00934661

Low Dose Extended-release Epidural and Lumbar Plexus Block Compared to Lumbar Plexus Block for Total Hip Resurfacing

Low Dose Extended-release Epidural Morphine in Conjunction With Lumbar Plexus Block Versus Lumbar Plexus Block Alone for Total Hip Resurfacing Arthroplasty: A Randomized Controlled Trial.

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Wake Forest University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

At Wake Forest University, the investigators have been using Extended Release Epidural Morphine (EREM), since late 2004, as part of multimodal analgesia in patients having gynecologic surgeries and hip arthroplasties. Hypothesis: In patients undergoing a Birmingham total hip arthroplasty (BHA), low dose EREM in conjunction with lumbar plexus block (LPB) will be better than lumbar plexus block alone in increasing proportion of patients who meet discharge criteria within 24 hours.

Detailed description

Extended release epidural morphine (EREM, DepoDur®: Endo Pharmaceuticals, Chadds Ford PA) has been studied and increasingly utilized as a method to allow for the improved post-operative analgesia of epidural analgesia without infusions. At Wake Forest University, the investigators have been using EREM, since late 2004, as part of multimodal analgesia in patients having gynecologic surgeries and hip arthroplasties. The investigators initially decreased our dosages from those recommended (15 mg for lower extremity surgery and 10-15 mg for abdominal surgery), because side effects (nausea, vomiting and hypotension) were felt to be limiting to recovery. The investigators now use 4-7.5 mg in most patients, with 7.5 mg being the exception and have achieved better results. For hip arthroplasties, the investigators currently use 4-5 mg and have performed two retrospective chart reviews on this use; both suggesting that this approach is efficacious. However, these doses have not been studied in a prospective, randomized, double blind trial. The investigators would like to evaluate the efficacy of this dose of EREM used as part of a multimodal regimen. The investigators will compare EREM 4 mg with lumbar plexus block versus lumbar plexus block alone, (providing the rest of our multimodal approach for both patients).

Conditions

Interventions

TypeNameDescription
DRUGExtended Release Epidural Morphine (EREM)A single Four mg (0.4 ml)dose of EREM will be administered into the epidural space and flushed with 1 ml of saline
DRUGPlaceboA single epidural injection will be a placebo consisting of 0.4 ml of saline followed by 1 ml saline flush

Timeline

Start date
2010-01-01
Primary completion
2013-03-01
Completion
2013-03-01
First posted
2009-07-08
Last updated
2018-09-12
Results posted
2018-01-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT00934661. Inclusion in this directory is not an endorsement.