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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-IOR-17011150 |
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Date of registration:
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2017-04-16 |
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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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Sufentanyl improves the analgesia effect of continuous femoral nerve block after total knee arthroplasty
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Scientific title:
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Sufentanyl improves the analgesia effect of continuous femoral nerve block after total knee arthroplasty |
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Date of first enrolment:
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2017-04-17 |
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Target sample size:
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Group SR:30;Group R:30; |
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Recruitment status: |
Recruiting |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=18663 |
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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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Quanguang Wang
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Address:
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Shangcai Villiage, Nanbaixiang Street, Ouhai District, Wenzhou, Zhejiang
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Telephone:
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+86 13736935500 |
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Email:
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quanguangwang@sina.com |
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Affiliation:
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The First Affiliated Hospital of Wenzhou Medical University |
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Name:
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Fangfang Xia
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Address:
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Shangcai Villiage, Nanbaixiang Street, Ouhai District, Wenzhou, Zhejiang
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Telephone:
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+86 13806622872 |
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Email:
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helenxia4271@163.com |
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Affiliation:
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The First Affiliated Hospital of Wenzhou Medical University |
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Key inclusion & exclusion criteria
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Inclusion criteria: patients scheduled for bilateral total knee arthroplasty were included into the study, aged 53~82years, weight 47~81kg, height 150~179cm, ASA I or II.
Exclusion criteria: Exclusion of neurologic or neuromuscular disease, allergy to local anesthetics, chronic opiate usage or unlikely to be fully cooperative during the study, such as having psychiatric disorders
Age minimum:
53
Age maximum:
82
Gender:
Both
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Health Condition(s) or Problem(s) studied
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total knee arthroplasty
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Intervention(s)
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Group SR:0.2% ropivacaine plus sufentanyl;Group R:0.2% ropivacaine;
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Primary Outcome(s)
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The intensity of postoperative pain of bilateral lower limbs;
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Secondary Outcome(s)
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patients’ degree of satisfaction about the analgesia of each side of the lower limb;The numbers of patients wakening up because of each side of the lower limb pain;the amount given by PCA;
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Source(s) of Monetary Support
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self-financing
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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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