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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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ChiCTR |
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Last refreshed on:
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18 April 2017 |
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Main ID: |
ChiCTR-IPC-14005348 |
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Date of registration:
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2014-10-17 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Propofol versus Propofol combined with Dezocine for flexible bronchoscopy: A Randomized Study
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Scientific title:
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Propofol versus Propofol combined with Dezocine for flexible bronchoscopy: A Randomized Study |
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Date of first enrolment:
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2014-11-01 |
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Target sample size:
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P:73;PD:73; |
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Recruitment status: |
Recruiting |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=9688 |
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Study type:
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Interventional study |
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Study design:
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Randomized parallel controlled trial
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Phase:
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I (Phase I study)
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Countries of recruitment
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China
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Contacts
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Name:
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Feng Yuan
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Address:
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No. 2, Jingba road of Jinshui District, Zhengzhou, China.
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Telephone:
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+86 13523099337 |
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Email:
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13523099337@163.com |
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Affiliation:
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The Second Affiliated Hospital of Zhengzhou University |
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Name:
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Tieli Dong
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Address:
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No. 2, Jingba road of Jinshui District, Zhengzhou, China.
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Telephone:
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+86 13783692658 |
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Email:
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tlddtl@126.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: The patients, aged between 18 to 75 years, with American Society of Anesthesiologists (ASA) physical classification system status of I to III.
Exclusion criteria: psychological disorders; hypersensitivity or allergy to the study drugs; uncontrolled hypertension (uncontrolled hypertension with blood pressure higher than 140/90 mmHg); major abnormalities of liver function; ischemic heart disease and severe respiratory disease.
Age minimum:
18
Age maximum:
75
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Propofol versus Propofol combined with Dezocine for flexible bronchoscopy
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Intervention(s)
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P:propofol ;PD:propofol combined with dezocine ;
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Primary Outcome(s)
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Pulse oxygen saturation;Heart rate;Mean arterial pressure;respiratory rates;time to initial sedation;total dosage of propofol;
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Secondary Outcome(s)
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cough scores;discomfort scores;
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Source(s) of Monetary Support
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self-raise
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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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