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

NCT ID: NCT01120951

Last Updated: 2010-05-18

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

COMPLETED

Total Enrollment

220 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-01-31

Study Completion Date

2010-04-30

Brief Summary

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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.

Detailed Description

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Conditions

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Respiratory Rate Changes

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Anaxsys Technology Ltd

INDUSTRY

Sponsor Role lead

Responsible Party

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Directorate of Anaesthesia, University Hospital of North Staffordshire, UK

Locations

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Papworth Hospital NHS Foundation Trust

Cambridge, Cambridgeshire, United Kingdom

Site Status

University Hospital of North Staffordshire

Stoke-on-Trent, Staffordshire, United Kingdom

Site Status

St. Peter's and Ashford Hospital NHS Trust

Guildford, Surrey, United Kingdom

Site Status

Russells Hall Hospital

Dudley, West Midlands, United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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ATL01009

Identifier Type: -

Identifier Source: org_study_id

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