Comparative Study of Nonintubated Uniport Thoracoscopic Surgery Using Thoracic Paravertebral Nerve Block Versus Intercostal Nerve Block for Peripheral Solitary Pulmonary Nodule Patients
NCT ID: NCT03086213
Last Updated: 2020-05-07
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
48 participants
INTERVENTIONAL
2017-03-01
2019-09-05
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.
Ultrasound-Guided Serratus Anterior Plane Block in Pneumothorax Surgery
NCT04191850
Comparative Study of Nonintubated Anesthesia Versus Intubated General Anesthesia in Single Port Thoracoscopic Bullectomy
NCT02109510
The Impact of Ultrasound-Guided Superficial and Deep Paravertebral Nerve Blocks at the Superior Costotransverse Ligament on Hemodynamics During the Induction Phase of Thoracoscopic Lung Lobectomy: A Multicenter, Double-Blind, Randomized Controlled Trial
NCT06841822
Ultrasound-Guided Serratus Anterior Plane Block for Additional Pain Relief After Lung Surgery
NCT04238455
Mid-point Transverse Process to Pleura Block Versus Thoracic Paravertebral Block in Posterolateral Thoracotomy
NCT06361121
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The initial experience of nonintubated thoracoscopic surgery included the intravenous controlled sedation and pain , thoracic epidural analgesia and thoracic vagus nerve block, due to series of adverse events of the epidural analgesia, operator was willing to perform the intrathoracic intercostal nerve block guided by camera during the operation and was considered as the simple and safety method for regional analgesia .However, the intercostal nerve block can not employ the adequate pain control ,after the surgery, the patient controlled analgesia is as usual needed.
The previous study showed that paravertebral block was the same effect on relieved pain as thoracic epidural analgesia and had the less complications such as hypotension, nausea or vomiting. With the advance in the technique of application of ultrasound, it is more interesting that using the ultrasound technique before the surgery is performed for the adequate pain control of the local regional analgesia in nonintubated surgery under spontaneous ventilation. However, ultrasound technique is difficult to have the skilled experience for the most anaesthetists and increase the related puncture complications such as hematoma, bleeding or pneumothorax. The method used study is guided by camera which is very simple and safety by avoidance of the puncture of the partial pleura or intercostal blood vessel, The investigators once used this approach for postoperative pain control under general intubation for lung cancer patients, so the investigators have had a skilled experience for achieving regional analgesia of nonintubated uniport thoracoscopic wedge resection.
So far, there has been no articles about thoracic paravertebral nerve block for regional analgesia of nonintubated thoracoscopic procedure patients. The investigators designed the study to compare the short term outcome on thoracic paravertebral nerve block in nonintubated technique with those of intercostal nerve block in uniport nonintubated video-assisted thoracoscopic surgery(VATS) as the control group.
This study will be performed at the third people's hospital of Shenzhen. A total of 48 patients will be enrolled(24 patients in each arms).
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
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
paravertebral nerve block group
non-intubated thoracic paravertebral nerve block of regional anesthesia Thoracic paravertebral nerve block of regional anesthesia at the T4 thoracic interspace
Propofol
anaesthetic
Sulfentanyl
anaesthetic
Dexmedetomidine
anaesthetic
Lidocaine
local anaesthetics
Ropivacaine
local anaesthetics
intercostals nerve block group
non-intubated intercostal nerve block of regional anesthesia Thoracic intercostal nerve block of regional anesthesia at the T3/4/5 thoracic interspace
Propofol
anaesthetic
Sulfentanyl
anaesthetic
Dexmedetomidine
anaesthetic
Lidocaine
local anaesthetics
Ropivacaine
local anaesthetics
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Propofol
anaesthetic
Sulfentanyl
anaesthetic
Dexmedetomidine
anaesthetic
Lidocaine
local anaesthetics
Ropivacaine
local anaesthetics
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* the undetermined peripheral solitary pulmonary nodule or tuberculoma was enrolled
* the well cardiopulmonary function
* age between 18 and 65 years old
* less airway secretion
* body mass index less than 25
* I to II grade of the American Society of Anesthesiologists
* no metabolic diseases
Exclusion Criteria
* the nodule of the nature of the non small cell lung caner is excluded
* hypovolemia, blood disorders or abnormal clotting mechanism
* the abnormal cardiopulmonary function(the American Society of Anesthesiologists greater than 3)
* lower airway infection,more than airway secretion
* abnormal anatomy of the spine,the history of thoracic back surgery
* impaired lung function(forced expiratory volume in second 1 less than predicted), or asthma uncontrolled on medications
* constrained cardiac output such as hypertrophic cardiomyopathy, mitral stenosis or complete atrioventricular block
* extensive pleural adhesion
* overweight (body mass index no less than 25)
* difficulty airway
* chronic pain score more than 5 before the surgery
* the history of bilateral thoracotomy
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Shenzhen Third People's Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
xia zhaohua
Director, Head of thoracic surgical department, Principal investigator, Associate clinical professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
the Third People's Hospital of Shenzhen
Shenzhen, Guangdong, China
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Statistical Analysis Plan
Document Type: Study Protocol
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
19800911
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.