Trials / Completed
CompletedNCT01993238
Evaluation of Procedural Analgesia for Liposonix Treatment
An Evaluation of Procedural Analgesia for Out-Patient Liposonix Treatment
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 11 (actual)
- Sponsor
- Solta Medical · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
The objectives of this study are to evaluate the safety and effectiveness of procedural analgesia for improvements in tolerability of treatment with the Liposonix System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Liposonix System (Model 2) | Treatment of subcutaneous adipose tissue of the abdomen using high intensity focused ultrasound (Liposonix System Model 2). |
| DRUG | Pre-treatment analgesia | Pre-treatment analgesia (combination of ondansetron, ketorolac, and hydromorphone) |
Timeline
- Start date
- 2013-11-01
- Primary completion
- 2014-01-01
- Completion
- 2014-01-01
- First posted
- 2013-11-25
- Last updated
- 2014-04-29
- Results posted
- 2014-04-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01993238. Inclusion in this directory is not an endorsement.