Trials / Unknown
UnknownNCT00737425
Safety and Efficacy Study of Pain Shield Device to Treat Subjects Following Laparoscopic-Assisted Abdominal Surgery
Evaluation of Safety and Efficacy of the PainShield Device for the Treatment of Subjects Who Underwent Laparoscopic-Assisted Abdominal Surgery
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- Sponsor
- Shaare Zedek Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate safety and efficacy of PainShield device, based on ultrasound technology, for postoperative pain relief and wound healing following a laparoscopic-assisted abdominal surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PainShield | |
| DEVICE | Sham PainShield |
Timeline
- Start date
- 2008-09-01
- First posted
- 2008-08-19
- Last updated
- 2008-10-28
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT00737425. Inclusion in this directory is not an endorsement.