Trials / Completed
CompletedNCT01806012
Use of the Enseal Intrument for Laparoscopic Supracervical Hysterectomy
Use of the Enseal Intrument for Laparoscopic Supracervical Hysterectomy: a Randomized, Single-Blinded Study Comparing the Efficacy to the Routine Procedure
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 160 (actual)
- Sponsor
- University Hospital Tuebingen · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The use of the EnSeal® instrument for laparoscopic supracervical hysterectomy in a randomized, single-blinded comparison to the conventional procedure. The objective of the study is to investigate if the use of the Enseal sealing instrument for supracervical hysterectomy leads to a shortening of the operation time.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Sealing tissue with the Enseal device | |
| PROCEDURE | Conventional supracervical hysterectomy |
Timeline
- Start date
- 2010-08-01
- Primary completion
- 2011-08-01
- Completion
- 2011-08-01
- First posted
- 2013-03-06
- Last updated
- 2013-03-06
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01806012. Inclusion in this directory is not an endorsement.