Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01641419

Trial Comparing Duration of Analgesia After Popliteal Fossa Sciatiac Nerve Block With Ropivacaine 0.5% When Combined With Placebo, Dexamethasone 4mg or Dexamethasone 8 mg

Randomized, Controlled Trial Comparing Duration of Analgesia After Popliteal Fossa Sciatiac Nerve Block With Ropivacaine 0.5% When Combined With Placebo, Dexamethasone 4mg or Dexamethasone 8 mg

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Baylor College of Medicine · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

The purpose is to find out if the addition of dexamethasone to ropivacaine 0.5% increases the duration of pain relief provided by popliteal sciatic nerve block performed for foot/ankle surgery. The investigators also want to find out if there is a difference between 4 and 8 mg dose of dexamethasone.

Conditions

Interventions

TypeNameDescription
DRUGPlacebo2 ml of saline added to 30 ml of ropivacaine 0.5% solution for nerve block
DRUGDexamethasone 4 mg2 ml of dexamethasone 4 mg solution added to 30 ml of ropivacaine 0.5% solution for nerve block
DRUGDexamethasone 8 mg2 ml of dexamethasone 8 mg solution added to 30 ml of ropivacaine 0.5% solution for nerve block

Timeline

Start date
2012-07-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2012-07-16
Last updated
2015-03-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01641419. Inclusion in this directory is not an endorsement.