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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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14 December 2015 |
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Main ID: |
NCT02362022 |
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Date of registration:
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04/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Effects of Morphine on Desflurane Consumption and Recovery Time
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Scientific title:
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Comparison of Two Different Doses of Intravenous Morphine on Desflurane Consumption and Recovery Time in Patients Undergoing Total Abdominal Hysterectomy |
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Date of first enrolment:
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September 2007 |
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Target sample size:
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90 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02362022 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator), 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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Turkey
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Contacts
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Name:
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cagla bali |
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Address:
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Telephone:
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Email:
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Affiliation:
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Baskent University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- undergoing total abdominal hysterectomy with general anaesthesia
Exclusion Criteria:
- renal dysfunction (cre>1.2), liver failure, cardiovascular, psychiatric, allergic and
metabolic disorders
Age minimum:
40 Years
Age maximum:
60 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Abdominal Hysterectomy (& Wertheim)
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Intervention(s)
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Drug: Morphine
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Primary Outcome(s)
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sedation scores for OASS scale
[Time Frame: postoperative first hour]
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postoperative desflurane consumption
[Time Frame: postoperative first hour]
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Secondary ID(s)
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14.09.2007/88-4
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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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