Prospective Evaluation of the Use of Thunderbeat Vessel Sealing Device in Laparoscopic Surgery
- Conditions
- Indication for Laparoscopic Surgery (Any)
- Registration Number
- NCT01999296
- Lead Sponsor
- Cantonal Hosptal, Baselland
- Brief Summary
All patients undergoing laparoscopic visceral and gynecologic procedures using the combined bipolar and ultrasonic vessel sealing and dissection device Thunderbeat are entered in a prospective registry. Data will be analysed concerning the safe use of the instrument and perioperative blood loss.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 250
Inclusion Criteria
- all patients undergoing laparoscopic visceral or gynecologic surgery
- need for a vessel sealing device during surgery
Exclusion Criteria
- non able to understand informed consent or missing consent
- age <18
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Use of additional vessel sealing devices one day Intra- and postoperative device-related complications 30 days
- Secondary Outcome Measures
Name Time Method Duration of Surgery one day Perioperative Blood Loss 30 days
Trial Locations
- Locations (1)
Kantonsspital Baselland Bruderholz
🇨🇭Bruderholz, Switzerland
Kantonsspital Baselland Bruderholz🇨🇭Bruderholz, Switzerland