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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-TRC-13003639 |
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Date of registration:
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2013-09-07 |
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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 application of Analgesia Nociception Index guided Remifentanil administration during general anesthesia for Spinal Surgery
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Scientific title:
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The application of Analgesia Nociception Index guided Remifentanil administration during general anesthesia for Spinal Surgery |
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Date of first enrolment:
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2012-09-13 |
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Target sample size:
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ANI group:30;control group:30; |
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Recruitment status: |
Completed |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=5921 |
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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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Other
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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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Duan Yi
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Address:
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49 North Garden Road, Haidian District, Beijing, China
100191
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Telephone:
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+86 18810533317 |
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Email:
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yiduan1987@163.com |
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Affiliation:
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Department of Anesthesia, Third Hospital, Peking University |
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Name:
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Liping Zhang
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Address:
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49 North Garden Road, Haidian District, Beijing, China
100191
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Telephone:
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+86 13911113805 |
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Email:
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lipingzhang01@aliyun.com |
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Affiliation:
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Department of Anesthesia, Third Hospital, Peking University |
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Key inclusion & exclusion criteria
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Inclusion criteria: ASA status I-II, aged 18-70 years, BMI 17-33kg.m-2, scheduled for elective posterior lumbar decompression and internal fixation for treatment of lumbar canal stenosis and/or lumbar disc herniation.
Exclusion criteria: pregnancy, non sinus rhythms, ANS altering diseases or medications, allergy to drugs used in this study ,baseline hemodynamic index that would be considered as abnormal(such as SBP>160mmHg or SBP<90mmHg,HR>90min-1or HR<45 min-1).
Age minimum:
18
Age maximum:
70
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Lumbar spinal stenosis and/or lumbar intervertebral disc herniation
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Intervention(s)
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ANI group:ANI guide the administration of remifentanil;control group:remifentanil was adapted by Anaesthesiologist corresponding to clinical experiences ;
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Primary Outcome(s)
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total number of unwanted events;the consumption of anesthetics;
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Source(s) of Monetary Support
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self-finacing
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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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