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

NCT ID: NCT01999296

Last Updated: 2015-07-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-10-31

Brief Summary

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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

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Conditions

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Indication for Laparoscopic Surgery (Any)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients undergoing laparoscopic surgery

Use of Thunderbeat (TM) in laparoscopic surgery

Intervention Type DEVICE

Interventions

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Use of Thunderbeat (TM) in laparoscopic surgery

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cantonal Hosptal, Baselland

OTHER

Sponsor Role lead

Responsible Party

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Daniel Steinemann, MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kantonsspital Baselland Bruderholz

Bruderholz, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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Thunderbeat in Laparoscopy

Identifier Type: -

Identifier Source: org_study_id

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