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Comparative Study of Nonintubated Uniport Thoracoscopic Surgery Using Thoracic Paravertebral Nerve Block Versus Intercostal Nerve Block for Peripheral Solitary Pulmonary Nodule Patients

S

Southern University of Science and Technology

Status

Completed

Conditions

Peripheral Solitary Pulmonary Nodule or Tuberculoma

Treatments

Drug: Propofol
Drug: Sulfentanyl
Drug: Dexmedetomidine
Drug: Ropivacaine
Drug: Lidocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT03086213
19800911

Details and patient eligibility

About

The aim of this study is to study the safety and effectiveness of the effects on the perioperative pain control comparing between the thoracic paravertebral nerve block using the camera guided and the intrathoracic intercostals nerve block for the management of nonintubated local regional analgesia in uniport thoracoscopic surgery for the undetermined solitary nodules patients.

Full description

Thoracoscopic minor lung resection has been the reasonable option for the diagnosis and treatment of management of the undetermined peripheral pulmonary nodules. Uniport procedure could reduce postoperative pain score, the length of hospital stay, moreover, nonintubated technique can avoid the disadvantages of conventional general anesthesia such as ventilator induced lung injury, sore throat or voice change. The nonintubated technique without tracheal intubation under spontaneous ventilation combined with uniport or single port thoracoscopic surgery has emerged as the least invasive procedure of wedge resection of peripheral pulmonary nodules, even the anatomical thoracoscopic lobectomy along with mediastinal lymph nodule dissection in case of the diagnosis of the primary lung cancer during the operation.

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).

Enrollment

48 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • written informed consent
  • 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

  • refusal or inability to comply with the informed consent
  • 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 2 patient groups

paravertebral nerve block group
Experimental group
Description:
non-intubated thoracic paravertebral nerve block of regional anesthesia Thoracic paravertebral nerve block of regional anesthesia at the T4 thoracic interspace
Treatment:
Drug: Lidocaine
Drug: Ropivacaine
Drug: Propofol
Drug: Sulfentanyl
Drug: Dexmedetomidine
intercostals nerve block group
Active Comparator group
Description:
non-intubated intercostal nerve block of regional anesthesia Thoracic intercostal nerve block of regional anesthesia at the T3/4/5 thoracic interspace
Treatment:
Drug: Lidocaine
Drug: Ropivacaine
Drug: Propofol
Drug: Sulfentanyl
Drug: Dexmedetomidine

Trial documents
3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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