Main
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Note: This record shows only 22 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. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT02091180 |
Date of registration:
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15/03/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Mannitol Improves Cerebral Oxygen Saturation
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Scientific title:
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Effect of Preoperative Mannitol Infusion on Cerebral Oxygen Saturation and Patients' Recovery After Laparoscopic Cholecystectomy |
Date of first enrolment:
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January 2013 |
Target sample size:
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40 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT02091180 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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Saudi Arabia
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Contacts
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Name:
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Hany A Mowafi, MD |
Address:
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Telephone:
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Email:
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Affiliation:
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University of Dammam |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- American Society of Anesthesiologists physical status I or II
- aged between 25 and 50 years
- with a body mass index (BMI) 22-34 kg/m2
Exclusion Criteria:
- obstructive or restrictive pulmonary disease
- cardiac dysfunction
Age minimum:
25 Years
Age maximum:
50 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Anesthesia
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Intervention(s)
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Drug: Mannitol
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Drug: Control
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Primary Outcome(s)
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rSO2
[Time Frame: participants will be followed for the duration of surgery, an expected average of 1 hour]
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Secondary Outcome(s)
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extubation time
[Time Frame: intraoperative]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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