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Clinical Assessment of the Use of the R8 Respiratory Rate Counter in Post-Operative Recovery in Adults and Adolescents

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01120951
First Posted: May 11, 2010
Last Update Posted: May 18, 2010
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. Read our disclaimer for details.
Information provided by:
Anaxsys Technology Ltd
  Purpose
The study aims to to establish whether or not measurement of respiratory rate taken using the Anaxsys Technology Ltd Respiratory Counter (R8 Counter) are equivalent to manual respiratory rate counting methods in patients receiving oxygen via a face mask.

Condition
Respiratory Rate Changes

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Clinical Assessment of the Use of the R8 Respiratory Rate Counter in Post-Operative Recovery in Adults and Adolescents

Further study details as provided by Anaxsys Technology Ltd:

Enrollment: 220
Study Start Date: January 2010
Study Completion Date: April 2010
Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   12 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Male or female patients aged 12 years and above following elective surgery under general anaesthesia
Criteria

Inclusion Criteria:

  • Male or female patients aged 12 years and above following elective surgery under general anaesthesia

Exclusion Criteria:

  • Patients admitted for emergency surgery
  • Patients having ASA rating of 3 or greater
  • Patients not receiving general anaesthesia
  • Patients expected to be in post-operative recovery for less than 15 minutes
  Contacts and Locations
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): NCT01120951


Locations
United Kingdom
Papworth Hospital NHS Foundation Trust
Cambridge, Cambridgeshire, United Kingdom, CB23 3RE
University Hospital of North Staffordshire
Stoke-on-Trent, Staffordshire, United Kingdom, ST4 6QG
St. Peter's and Ashford Hospital NHS Trust
Guildford, Surrey, United Kingdom, KT16 0PZ
Russells Hall Hospital
Dudley, West Midlands, United Kingdom, DY1 2HQ
Sponsors and Collaborators
Anaxsys Technology Ltd
  More Information

Responsible Party: Dr Ian Smith, Directorate of Anaesthesia, University Hospital of North Staffordshire, UK
ClinicalTrials.gov Identifier: NCT01120951     History of Changes
Other Study ID Numbers: ATL01009
First Submitted: May 9, 2010
First Posted: May 11, 2010
Last Update Posted: May 18, 2010
Last Verified: May 2010

Keywords provided by Anaxsys Technology Ltd:
Respiratory rate R8 Anaxsys