Trials / Completed
CompletedNCT01706588
Injectable Diclofenac for the Prevention of Post-operative Dental Pain
Preliminary Evaluation of the Efficacy and Local Tolerability of Injectable Diclofenac at 5, 12.5, 25 and 50 mg/mL, Administered Locally Prior to Surgery for the Prevention of Post-operative Pain After Third Molar Surgery
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 75 (actual)
- Sponsor
- IBSA Institut Biochimique SA · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, randomised, double-blind, placebo-controlled, parallel group study in approximately 75 patients undergoing surgical removal of an impacted lower third molar.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Diclofenac sodium | One single diclofenac injection into the surgical area before surgery but as soon as the anaesthetic has taken effect. |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2013-05-01
- Completion
- 2013-05-01
- First posted
- 2012-10-15
- Last updated
- 2014-09-05
- Results posted
- 2014-08-28
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT01706588. Inclusion in this directory is not an endorsement.