Trials / Completed
CompletedNCT00564785
Synera™ for Epidural Needle Insertion
A Randomized, Double-Blind, Controlled Trial of the Synera™ vs. Lidocaine for Epidural Needle Insertion in Laboring Women
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 33 (actual)
- Sponsor
- IWK Health Centre · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
We hypothesized that the analgesic effect of Synera™ analgesic patch would be superior to traditional infiltration with lidocaine for pain of epidural needle insertion in laboring parturients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Synera(TM) | Synera(TM) patch applied 20 minutes prior to epidural |
| OTHER | Placebo patch | placebo patch applied 20 minutes prior to epidural |
Timeline
- Start date
- 2007-02-01
- Completion
- 2007-03-01
- First posted
- 2007-11-28
- Last updated
- 2007-11-28
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00564785. Inclusion in this directory is not an endorsement.