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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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TCTR |
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Last refreshed on:
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29 April 2024 |
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Main ID: |
TCTR20140903003 |
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Date of registration:
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03/09/2014 |
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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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Direct field block with 40 ml of 0.125%Bupivacaine improved postoperative pain control after C/S on the top of spinal morphine
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Scientific title:
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Direct field block with 40 ml of 0.125%Bupivacaine improved postoperative pain control after C/S on the top of spinal morphine |
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Date of first enrolment:
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31/08/2014 |
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Target sample size:
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Recruitment status: |
Completed |
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URL:
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https://www.thaiclinicaltrials.org/show/TCTR20140903003 |
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Study type:
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Interventional |
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Study design:
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Randomized
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Phase:
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Phase 4
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Countries of recruitment
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Thailand
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Contacts
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Name:
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Thitima
Chinachoti |
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Address:
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Department of Anesthesiology,Sayammin Building 11th floor,Faculty of Medicine Siriraj Hospital, Mahi
10700
Bangkok
Thailand |
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Telephone:
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6681-308-2438 |
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Email:
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sitci35@gmail.com |
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Affiliation:
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Faculty of Medicine Siriraj Hospital, Mahidol University |
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Name:
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Thitima
Chinachoti |
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Address:
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Department of Anesthesiology, Sayammin Building 11th floor, Faculty of Medicine Siriraj Hospital, Ma
10700
Bangkok
Thailand |
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Telephone:
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6681-308-2438 |
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Email:
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sitci35@gmail.com |
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Affiliation:
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Faculty of Medicine Siriraj Hospital, Mahidol University |
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Key inclusion & exclusion criteria
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Inclusion criteria: Parturient undergoing non-emergency cesarean delivery under spinal anesthesia
ASA class I-II, having a full understanding of the question in this trial
Exclusion criteria: Patients with pre-eclampsia
History of progressive neurological deficit or any contraindications for spinal anesthesia
Allergy to the medication used in this trial including local anesthetic, opioid, parecoxib, paracetamol or history of drug abuse
Age minimum:
18 Years
Age maximum:
50 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Direct field block
Transversus abdominis plane block
Postoperative analgesia after cesarean section
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Effectiveness of direct field block on the top of intrathecal morphine
Postoperative analgesia after cesarean section
Direct field block
Transversus abdominis plane block
Postoperative analgesia after cesarean section
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Intervention(s)
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Local infiltration with 40 ml of 0.125% bupivacaine at incisional margin along transversus plane, anterior and posterior rectus sheath at wound closure on the top of spinal block,Spinal block with 0.5% bupivacaine with 0.2 mg morphine total 2.2 ml
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Transversus abdominis plane block,Spinal block alone
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Experimental Drug,No Intervention No treatment
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Primary Outcome(s)
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Postoperative pain free period 48 hours postoperative Pain Numeric Rating Scale
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Secondary Outcome(s)
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Morphine comsumption in 24 hours 24 hours postoperative Milligram
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Source(s) of Monetary Support
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Self support
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Ethics review
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Status: Submitted, approved
Approval date:
Contact:
siethics@mahidol.ac.th
Siriraj Institutional Review Board
662-419-2667-72 Ext.
siethics@mahidol.ac.th
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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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31/08/2014 |
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URL:
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