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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04426097
Other study ID # TMU-JIRB N201803027
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date July 1, 2022

Study information

Verified date March 2020
Source Taipei Medical University WanFang Hospital
Contact Lin Jui An, PhD
Phone +886-66382736,
Email greenscatter1031@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Currently, there is a trend toward non-intubated anesthesia methods for video-assisted thoracic surgery in our hospital. During the surgery, intrathoracic vagus nerve blockade is suggested for inhibit cough reflex in previous paper. However, right and left side of vagus nerves both deep near the aorta or trachea respectively. To achieving the procedure may induce cough reflex by lobar traction even result vital organ damage. This study aims to apply alternative vagus nerve blockade at neck level via ultrasound guidance and test if the procedure real reduce cough reflex then previous method. We also follow up the patient's vital sign, vocal cord and diaphragm movement, horner syndrome and hoarseness to evaluating if cervical vagal blockade has the potential risk involve other surrounding nerves


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Study Design


Related Conditions & MeSH terms

  • Video-assisted Thoracoscopic Surgery

Intervention

Procedure:
Cervical Vagal Blockade
Cervical Vagal Blockade with 0.5 % ropivacaine 2.5 ml and 2% xylocaine 2.5 ml
Without Blockade
Without Blockade

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

References & Publications (9)

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Outcome

Type Measure Description Time frame Safety issue
Primary Effect of Cervical Vagal Blockade on Cough Incidence number of coughing episodes During the VATS procedure
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