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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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KCT |
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Last refreshed on:
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24 June 2021 |
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Main ID: |
KCT0006271 |
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Date of registration:
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2021-06-18 |
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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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Compared the Analgesic effects of Ultrasound-guided single-dose Paravertebral Nerve Block and Erector Spinae Plane Block for Videoscopic assisted Thoracic Surgery
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Scientific title:
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Compared the Analgesic effects of Ultrasound-guided single-dose Paravertebral Nerve Block and Erector Spinae Plane Block for Videoscopic assisted Thoracic Surgery |
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Date of first enrolment:
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2021-06-09 |
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Target sample size:
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52 |
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Recruitment status: |
Not yet recruiting |
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URL:
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https://cris.nih.go.kr/cris/search/detailSearchEn.do?seq=19598 |
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Study type:
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Interventional Study |
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Study design:
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Primary Purpose : Treatment, Intervention Model : Parallel, Blinding/Masking : Single, Blinding Target : Subject, Allocation : RCT
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Phase:
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Not applicable
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Countries of recruitment
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Korea, Republic of
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Contacts
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Name:
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HYEJIN
DO |
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Address:
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20, Ilsan-ro, Wonju-si, Kangwon-do
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Telephone:
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+82-33-742-1536 |
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Email:
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dohyejin@yonsei.ac.kr |
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Affiliation:
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Yonsei University, Wonju Severance Christian Hospital |
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Name:
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JI HYUNG
PARK |
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Address:
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20, Ilsan-ro, Wonju-si, Kangwon-do
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Telephone:
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+82-33-742-1536 |
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Email:
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killerjhjh@naver.com |
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Affiliation:
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Yonsei University, Wonju Severance Christian Hospital |
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Key inclusion & exclusion criteria
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Inclusion criteria: - Among patients undergoing video assisted thoracic surgery, those who agreed to the pain control technique.
- Age: 19 to 80 years old
- ASA (American Society of Anesthesiologists Class) I-?
Exclusion criteria: - Patients who have difficulty in obtaining information and effects of nerve block related to the study due to cognitive decline.
- Patients who are contraindicated in nerve block. (INR>1.3 PTT>43 seconds without anticoagulant administration, coagulopathy, antiplatelet drug use within 48 hours, double antiplatelet therapy, surgical site infection, patient's refusal of procedure, allergic reaction to local anesthetic)
- Patients requiring therapeutic anticoagulant therapy after surgery.
- Pregnant woman
- Concomitant diseases: All comorbid diseases that the patient should be excluded from the study under the judgment of the anesthesiologist (sepsis, anatomical thoracic deformity, empyema, increased intracranial pressure, etc.)
Age minimum:
19?(Year)
Age maximum:
80?(Year)
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Diseases of the respiratory system
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Intervention(s)
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Procedure/Surgery : Following thoracic epidural block, which is considered the standard treatment for postoperative pain control, for patients who underwent video assisted thoracic surgery, paravertebral nerve block has been proven to be effective in pain control. Recently, a new technique called erector spinae plane block has been introduced and the frequency of its use is gradually increasing. The difference between the two procedures is the target point where the tip of the epidural needle inserted under ultrasound guidance is located. In the case of paravertebral nerve block, the needle tip is placed in the paravertebral space located between the transverse process, superior costotransverse ligament, intertransverse ligament, and the pleural structure, and then a local anesthetic is administered. In the case of erector spinae plane block, after checking the trapezius, rhomboids, erector spinae, and transverse processes, place the needle tip under the erector spinae muscle and administer a local anesthetic.
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Primary Outcome(s)
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VAS (Visual analog scale) of each group after surgery
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Secondary Outcome(s)
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Total consumption of opioids (Morphine equivalent dose)
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Analgesics taken by the patient in addition to the nerve block
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Source(s) of Monetary Support
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Yonsei University, Wonju Severance Christian Hospital
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Ethics review
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Status: Submitted approval
Approval date: 18/05/2021
Contact:
+82-33-741-1703
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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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