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the Clinicaltrail of the Effection Which of Phrenic Block Using in Non-intubated Video-assisted Thoracoscopic Surgery

S

Southern University of Science and Technology

Status and phase

Unknown
Early Phase 1

Conditions

Phrenic Nerve Paralysis

Treatments

Procedure: phrenic block
Procedure: no phrenic block

Study type

Interventional

Funder types

Other

Identifiers

NCT03653494
daizhongliang-02

Details and patient eligibility

About

Putting 80 patients divided into group S(non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia and Vagus block) and group D(non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia、Vagus block and Phrenic block)randomly,compare the volume of anesthetic and the number of increasing anesthetic during operation were compared between the two groups.If the date of group S greater than group D,it shows that the effect of anesthetic effect of group D is better than group S.

Full description

  1. Put 80 patients divided into group S(non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia and Vagus block) and group D(non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia、Vagus block and Phrenic block)randomly.
  2. Compare the volume of anesthetic drugs between the two groups.
  3. If the date of group S greater than group D,it shows that the effect of anesthetic effect of group D is better than group S.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patient agreed to perform non-intubated video-assisted thoracoscopic surgery, and informed the possibility of intraoperative tracheal intubation or thoracotomy.
  • No conventional anesthesia contraindication, no history of thoracic surgery, good cardiopulmonary function.
  • There is no severe adhesion and calcification in the thoracic cavity, and no artificial pneumothorax is affected.
  • the patient has no serious anxiety or depression.
  • Small surgical trauma, simple steps, short time.

Exclusion criteria

  • Mallampati≥3.
  • BMI≥26 kg/m2.
  • Hemodynamic instability.
  • INR≥1.5.
  • Respiratory infection, persistent cough or airway mucus hypersecretion, high risk of reflux.
  • nervous system disease,such as seizure or brain edema.
  • Extensive pleural adhesions or once chest surgery.
  • PaO2<60mmHg or PaCO2>50 mmHg.
  • Central hypopnea syndrome.
  • Lung isolation should be used to protect the healthy side of the lung.
  • Complicated operation, large trauma, long time, lack of experience or poor cooperation in the surgical team.
  • Contraindications to local anesthetic.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

80 participants in 2 patient groups

phrenic block group
Experimental group
Description:
non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia、Vagus block and Phrenic block
Treatment:
Procedure: phrenic block
Control group
Active Comparator group
Description:
non-intubated general anesthesia combine with Paravertebral blocks、surface spray anesthesia and Vagus block
Treatment:
Procedure: no phrenic block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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