- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05042583
Effect of Ultrasound-guided Left Stellate Ganglion Block on Rapid Recovery in Patients With Liver Lobectomy and Its Mechanism
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: zhonghua chen, master's degree
- Phone Number: 13625751526
- Email: chenbeijing116@163.com
Study Locations
-
-
Zhejiang
-
Shaoxing, Zhejiang, China, 312000
- Recruiting
- Shaoxing People's Hospital
-
Contact:
- zhonghua chen, master's degree
- Phone Number: 18279563090
- Email: 429065940@qq.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:Sixty patients with elective lobectomy; heart function grade I or II;ASA grade I or II;aged 18-70 years.
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Exclusion Criteria:Non-lobectomy patients; age <18 and > 70 years old;heart function grade ≥ III, ASA grade ≥ III; Hypersensitivity to local anesthesia;combined with immune disease or immunosuppression;severe mental illness unable to cooperate with SGB;abnormal neck anatomy;Stellate ganglion block failure;the patient refused to participate in the study.
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Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
The experimental group was injected with 0.5% ropivacaine 6ml
|
The probe direction was 30-45 degrees from the sagittal plane of the neck.
The anterior nodules of the transverse process of the sixth cervical vertebra were displayed.
The important anatomical structures were distinguished, and the internal carotid artery and longus cervical muscle were observed.
A 25G, 6cm puncture needle was used with the tip beveled downward, and the needle path and tip were shown under ultrasound.
The tip reached the high-echo sieve structure between the carotid artery and longus cervical muscle, and the drug solution was injected after withdrawal without blood and gas .
The experimental group was injected with 6ml 0.5% ropivacaine.
|
|
Placebo Comparator: Control group
control group was injected with 6ml normal saline.
|
The probe direction was 30-45 degrees from the sagittal plane of the neck.
The anterior nodules of the transverse process of the sixth cervical vertebra were displayed.
The important anatomical structures were distinguished, and the internal carotid artery and longus cervical muscle were observed.
A 25G, 6cm puncture needle was used with the tip beveled downward, and the needle path and tip were shown under ultrasound.
The tip reached the high-echo sieve structure between the carotid artery and longus cervical muscle, and the drug solution was injected after withdrawal without blood and gas .
The experimental group was injected with 6ml 0.5% ropivacaine.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative complications
Time Frame: Within one week after surgery
|
pulmonary infection, oxygenation injury, arrhythmia, bleeding, intestinal paralysis, incision infection, renal insufficiency, cognitive dysfunction, etc.
|
Within one week after surgery
|
|
mortality rate
Time Frame: Within 30 days after surgery
|
mortality rate
|
Within 30 days after surgery
|
|
Plasma concentrations of IL-6,IL-10 and TNF-α
Time Frame: Within three days of the surgery
|
Plasma concentrations of IL-6,IL-10 and TNF-α were measured before operation, 6 h after operation, 24 h after operation, and 72 h after operation
|
Within three days of the surgery
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1 (Other Identifier: Mobile Health and Wellness Program)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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