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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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SLCTR |
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Last refreshed on:
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27 April 2013 |
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Main ID: |
SLCTR/2012/006 |
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Date of registration:
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13/06/2012 |
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Primary sponsor: |
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Public title:
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A study to determine the improvement of oxygenation by adopting the normal sleeping body position in individuals during artificial ventilation
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Scientific title:
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A study to determine the improvement of oxygenation by adopting the normal sleeping body position in individuals during artificial ventilation |
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Date of first enrolment:
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1/8/2012 |
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Target sample size:
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174 (87 subjects per group) |
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Recruitment status: |
Pending |
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URL:
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http://www.slctr.lk/trial_details.asp?reg_id={AD5DB50F-7301-48F2-9337-CA5A37C381FE} |
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Study type:
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Interventional |
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Study design:
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Single center, single blind, parallel group, randomized controlled trial
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Countries of recruitment
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Sri Lanka
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Contacts
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Name:
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Dr. Vasanthi Pinto
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Address:
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Department of Anaesthesiology, Faculty of Medicine, Peradeniya, Sri Lanka
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Telephone:
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0773662199 |
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Email:
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vasantipinto@yahoo.com |
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Affiliation:
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Consultant Anaesthetist , Senior Lecturer |
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Name:
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Dr. Vasanthi Pinto
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Address:
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Department of Anaesthesiology, Faculty of Medicine, University of Peradeniya, Sri Lanka
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Telephone:
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0773662199 |
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Email:
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vasantipinto@yahoo.com |
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Affiliation:
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Consultant Anaesthetist, Senior Lecturer |
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Key inclusion & exclusion criteria
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Inclusion criteria: Patients receiving mechanical ventilation in SIMV mode
Exclusion criteria: Asthma, COPD, segmental lung pathologies, chest deformities, cerebral oedema with evidence of raised intracranial pressure, clinical conditions that may contraindicate the change of position such as fractures, spinal injuries, haemodynamic instability
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Oxygenation in ventilated patients
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Intervention(s)
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Following randomization, the following will be carried out on the intervention group:
1.Stabilization in semi recumbent position (the normal nursing position in ICU)
2.Patients placed in normal sleeping position (head and arm position) for 1 hour
3.Return to semi recumbent position
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Primary Outcome(s)
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1. Arterial blood gas readings
2. Arterial oxygen saturation
3. Spontaneous tidal volume
4. Respiratory rate
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Secondary Outcome(s)
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1.Time taken to wean from the ventilator
2. Mortality at the discharge from the ICU
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Source(s) of Monetary Support
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None
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