Inadequate Emergence After Laparoscopic Surgery in Trendelemburg Position

Sponsor
Corporacion Parc Tauli (Other)
Overall Status
Unknown status
CT.gov ID
NCT02101671
Collaborator
(none)
140
1
7
19.9

Study Details

Study Description

Brief Summary

The purpose of this study is to determinate if the patients submitted to laparoscopic surgery in trendelemburg position develope more inadequate anaesthesic emergence than patients submitted to laparoscopic surgery in other positions.

Study Design

Study Type:
Observational
Anticipated Enrollment :
140 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Inadequate Emergence After Anaesthesia in Laparoscopic Surgery in Trendelemburg Position
Study Start Date :
May 1, 2014
Anticipated Primary Completion Date :
Aug 1, 2014
Anticipated Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
trendelemburg positioning

Patients undergone laparoscopic surgery in trendelemburg position

Not trendelemburg positioning

Patients undergone laparoscopic surgery not in trendelemburg position

Outcome Measures

Primary Outcome Measures

  1. Inadequate emergence after anaesthesia [10 minutes after the arrival of the patient in the postsurgical unit]

    The inadequate emergence after anaesthesia will be evalueted with the Richmond Agitation Sedation Scale, defining as inadequate emergence a punctuation >= +1 (delirium form) and <=-2 (hypoactive form).

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • laparoscopic surgery

  • general anaesthesia

  • trendelemburg positioning

  • extubated in the operatory theater

Exclusion Criteria:
  • unable of communicate

  • dementia

  • psychiatric history

  • neurosurgery

  • alchohol and drugs addictions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Anaesthesia and Reanimation Department, Hospital Parc Tauli Sabadell Barcelona Spain 08208

Sponsors and Collaborators

  • Corporacion Parc Tauli

Investigators

  • Principal Investigator: Morena Basso, Corporacion Parc Tauli

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Morena Basso, MD, Corporacion Parc Tauli
ClinicalTrials.gov Identifier:
NCT02101671
Other Study ID Numbers:
  • 2014/522
First Posted:
Apr 2, 2014
Last Update Posted:
Apr 2, 2014
Last Verified:
Mar 1, 2014

Study Results

No Results Posted as of Apr 2, 2014