Ultrasound-guided Continuous Low Serratus Anterior Plane Block in Hepatocellular Carcinoma Surgery
NCT ID: NCT05531864
Last Updated: 2024-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
160 participants
INTERVENTIONAL
2021-01-01
2024-02-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effectivity and Safety of Ultrasound-guided Percutaneously Radiofrequency Ablation for Liver Cancer
NCT03026452
Laparoscopic Associating Liver Partition and Portal Vein Ligation for Staged Hepatectomy
NCT02203409
Effects of Anesthetic Methods on Hepatic Cancer Cell Malignancy
NCT03594188
Surgical Specification and Efficacy Evaluation of Total Laparoscopic Left Liver Resection
NCT02131441
Laparoscopic Versus Open Liver Resection for Hepatocellular Carcinoma
NCT02526043
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Continuous serratus anterior plane block
Ultrasound-guided continuous serratus anterior plane block.
Ultrasound-guided continuous low serratus anterior plane block
Low anterior serratus plane block, move the mid-axillary line 4 and 5 intercostal puncture points are moved down and the puncture is changed to 7 and 8 intercostal.
Single serratus anterior plane block combined with rectus sheath nerve block
Ultrasound-guided single serratus anterior plane block combined with rectus sheath nerve block.
Ultrasound-guided single serratus anterior plane block
Ultrasound-guided single anterior saw plane block was performed, and a needle was injected between the 4th and 5th costals in the midaxillary line.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Ultrasound-guided continuous low serratus anterior plane block
Low anterior serratus plane block, move the mid-axillary line 4 and 5 intercostal puncture points are moved down and the puncture is changed to 7 and 8 intercostal.
Ultrasound-guided single serratus anterior plane block
Ultrasound-guided single anterior saw plane block was performed, and a needle was injected between the 4th and 5th costals in the midaxillary line.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. ASAI-II;
3. BMI: 18-29 kg/m2
Exclusion Criteria
2. Comorbid psychiatric and neuromuscular disorders;
3. A history of allergy to anesthetic drugs;
4. Participation in other recent clinical or drug trials.
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Liu Di
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Liu Di
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
ailing wu, Doctor
Role: STUDY_DIRECTOR
First People's Hospital of Neijiang.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The First People's Hospital of Neijiang
Neijiang, Sichuan, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Hengchun Shen, master
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
JF20PJ288
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.