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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-11001192 |
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Date of registration:
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2011-02-23 |
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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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Efficacy of ultrasound-guided transversus abdominis plane (TAP) block as postoperative analgesia in unilateral hernioplasty surgery: a randomized controlled trail
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Scientific title:
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Efficacy of ultrasound-guided transversus abdominis plane (TAP) block as postoperative analgesia in unilateral hernioplasty surgery: a randomized controlled trail |
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Date of first enrolment:
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2011-02-01 |
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Target sample size:
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Group A:20;Group B:20;Group C:20;Group D:20;Group E:20; |
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Recruitment status: |
Completed |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=8347 |
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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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Xue Tian
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Address:
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Central Operating Room, 4th Floor, Clinic Building, Peking University Peaple's Hospital
100044
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Telephone:
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+86 010 88325581 |
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Email:
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justine_troy@163.com |
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Affiliation:
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Peking University People's Hospital |
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Name:
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Yi Feng
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Address:
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Central Operating Room, Floor 4, Clinic Building, Peking University Peaple's Hospital
100044
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Telephone:
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+86 010 88325581 |
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Email:
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yifeng65@sina.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. Aged 18 to 70 years old;
2. ASA I/II;
3. Underwent unilateral hernioplasty surgery;
4. Suitable for local anaethesia;
5. Negative of cognitive/expressive dysfunction, accept post-operative analgesia out of free will, and sign the consent form.
Exclusion criteria: 1. Reject relative procedure;
2. Procedure failed.
Age minimum:
18
Age maximum:
79
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Acute pain
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R52.051
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Intervention(s)
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Group A:0.9% NaCl surgery side transversus abdominis plane block ;Group B:0.1% ropivacaine surgery side transversus abdominis plane block;Group C:0.25% ropivacaine surgery side transversus abdominis plane block ;Group D:0.375% ropivacaine surgery side transversus abdominis plane block ;Group E:0.5% ropivacaine surgery side transversus abdominis plane block ;
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Primary Outcome(s)
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Visual Analogue Scales;Satisfaction of analgesia;Using of remedial medicine;
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Secondary Outcome(s)
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Plane of blocking;First time of flatus/ defecation;First time of pain feeled;First time of standing/ walking with assistance;Vital signs;
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Source(s) of Monetary Support
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Self -funding
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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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