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Prospective Evaluation of the Use of Thunderbeat Vessel Sealing Device in Laparoscopic Surgery

NCT01999296 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2015-07-17

No results posted yet for this study

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.

Conditions

  • Indication for Laparoscopic Surgery (Any)

Interventions

DEVICE

Use of Thunderbeat (TM) in laparoscopic surgery

Sponsors & Collaborators

  • Cantonal Hosptal, Baselland

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2015-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01999296 on ClinicalTrials.gov