Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

MinIAttention - Attention Management in Minimal Invasive Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03363152
Recruitment Status : Recruiting
First Posted : December 6, 2017
Last Update Posted : December 6, 2017
Sponsor:
Information provided by (Responsible Party):
Klugsberger Bettina, Ludwig Boltzmann Institute for Operative Laparoscopy

Brief Summary:
Laparoscopic surgical suboptimal outcomes in patient safety measures are correlated with (i) cognitive load / level of attention of the operating surgeon, (ii) the frequency and degree of disruptions to the surgical workflow, and (iii) the misalignment of visual and motor axes in laparoscopic equipment / setting (eye-hand coordination).

Condition or disease
Disturbance of Attention

  Show Detailed Description

Layout table for study information
Study Type : Observational
Estimated Enrollment : 42 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: MinIAttention - Attention Management in Minimal Invasive Surgery
Actual Study Start Date : July 6, 2016
Estimated Primary Completion Date : January 30, 2019
Estimated Study Completion Date : December 30, 2020



Primary Outcome Measures :
  1. surgeon´s attention [ Time Frame: july 2017 until December 2019 ]
    surgeon´s attention during laparoscopic surgery



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Sampling Method:   Non-Probability Sample
Study Population
surgeons for General and Visceral surgery
Criteria

Inclusion Criteria:

  • laparoscopic cholecystectomy

Exclusion Criteria:

  • open surgical procedures

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03363152


Contacts
Layout table for location contacts
Contact: Andreas Shamiyeh, Prof. Dr. +4357680832133 andreas.shamiyeh@kepleruniklinikum.at
Contact: Alois Ferscha, Prof. Dr. +43-732-2468-4760 ferscha@pervasive.jku.at

Locations
Layout table for location information
Austria
Kepler university clinic Recruiting
Linz, Upper Austria, Austria, 4020
Contact: Andreas Shamiyeh, Prof. Dr.    +4357680832133    andreas.shamiyeh@kepleruniklinikum.at   
Sponsors and Collaborators
Ludwig Boltzmann Institute for Operative Laparoscopy

Publications:
Layout table for additonal information
Responsible Party: Klugsberger Bettina, Dr. Bettina Klugsberger, Ludwig Boltzmann Institute for Operative Laparoscopy
ClinicalTrials.gov Identifier: NCT03363152     History of Changes
Other Study ID Numbers: Minatt-017
First Posted: December 6, 2017    Key Record Dates
Last Update Posted: December 6, 2017
Last Verified: November 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No