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:
Information provided by:
Anaxsys Technology Ltd
ClinicalTrials.gov Identifier:
NCT01120951
First received: May 9, 2010
Last updated: May 17, 2010
Last verified: May 2010
  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

Ages Eligible for Study:   12 Years and older
Genders Eligible for Study:   Both
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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

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
Study First Received: May 9, 2010
Last Updated: May 17, 2010
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency

Keywords provided by Anaxsys Technology Ltd:
Respiratory rate R8 Anaxsys

ClinicalTrials.gov processed this record on July 23, 2014