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Vagus Nerve Preservation and Chronic Cough in Non-small Cell Lung Cancer Surgery

Primary Purpose

Lung Cancer, Vagus Nerve Injuries, Cough

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Pulmonary branch of vagus nerve preserved
Pulmonary branch of vagus nerve not preserved
Sponsored by
Seoul National University Bundang Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subjects clearly understand the purpose of the study, are willing and able to comply with the requirements to complete the study, and can sign the informed consent.
  2. Clinically suspicious of non-small cell lung cancer or tissue confirmed preoperatively
  3. Clinical stage T1-3/N0-1/M0
  4. Preoperative ECOG performance status 0-1
  5. Preoperative ASA class I-III
  6. Preoperative pulmonary function test FEV1 ≥ 60%, DLCO ≥ 60%
  7. Patients expected to achieve R0 (complete resection) via simple lobectomy and mediastinal lymph node dissection

Exclusion Criteria:

  1. Patients who smoked within 2 weeks prior to operation
  2. Patients who received antitussives and expectorants 2 weeks prior to operation
  3. Patients who are pregnant or breast feeding
  4. Patients with severe or uncontrolled psychological disorders
  5. Patients with severe pulmonary adhesion
  6. Patients who are ineligible for minimally invasive surgery; thoracotomy conversion
  7. Patients diagnosed with other malignancies within 2 years prior to operation
  8. Patients who received chemotherapy or radiotherapy within 6 months prior to operation
  9. Patients suspicious of clinical N2 or received neoadjuvant therapy prior to operation
  10. Patients with cough-related diseases; COPD, asthma, ILD, GERD
  11. Patients suspicious of lymph node metastasis/invasion around vagus nerve during the preoperative clinical staging evaluation

Sites / Locations

  • Seoul National UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Pulmonary branch of vagus nerve preserved

Pulmonary branch of vagus nerve not-preserved

Arm Description

Pulmonary branch of vagus nerve is preserved during the mediastinal lymph node dissection using minimally invasive surgery

Pulmonary branch of vagus nerve is not preserved during the mediastinal lymph node dissection using minimally invasive surgery

Outcomes

Primary Outcome Measures

Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Qualitative measurement of postoperative cough
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Quantitative measurement of postoperative cough
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.

Secondary Outcome Measures

Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Pulmonary function test
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Pulmonary function test
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Pulmonary function test
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Pulmonary function test
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Pulmonary function test
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Incidence of postoperative pulmonary complications, hospital stay and readmission, ICU care
Histopathologic review of the total number of mediastinal lymph node dissected
Total number of dissected mediastinal lymph nodes and metastatic lymph nodes will be analyzed. Patient's preoperative clinical N stage and pathologic N stage will be compared; if pathologic N stage is higher than that of the clinical N stage, it will be considered as nodal upstaging.

Full Information

First Posted
May 23, 2021
Last Updated
October 24, 2022
Sponsor
Seoul National University Bundang Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04923412
Brief Title
Vagus Nerve Preservation and Chronic Cough in Non-small Cell Lung Cancer Surgery
Official Title
Prospective Randomized Controlled Study on the Effects of Vagus Nerve Pulmonary Branch Preservation During Video-assisted Thoracic Surgery Lobectomy in Non-small Cell Lung Cancer: Can it Decrease Postoperative Cough and Pulmonary Complications
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Bundang Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Lung cancer is the leading cause of cancer death worldwide. Surgical resection is the main treatment for resectable non-small-cell lung cancer (NSCLC), and lobectomy with systemic mediastinal lymph node dissection is the standard surgical method. However, a significant number of patients experience postoperative chronic cough; it is observed in about 60% of patients during the first year of outpatient clinic follow-up, and persistently lasts in about 24.7-50% during the 5 year follow-up period. Several studies showed the association between vagus nerve and chronic cough. The bronchopulmonary vagal afferent C-fibers are responsible for cough, chest tightness and reflex bronchoconstrictions. It is expected that during the mediastinal lymph node dissection, the inevitable injuries to the pulmonary branch of vagus nerve is largely responsible for development of chronic cough. In other words, preservation of pulmonary branch of vagus nerve may reduce the incidence of chronic cough and relevant detrimental effects on quality of life. Therefore, this prospective, randomized and controlled clinical study, aims to evaluate the effect of vagus nerve preservation on postoperative chronic cough in patients undergoing lobectomy with mediastinal lymph node dissection. In addition, the feasibility and oncologic safety of preserving pulmonary branch of vagus nerve during mediastinal lymph node dissection with minimally invasive surgery compared with conventional mediastinal lymph node dissection with minimally invasive surgery will also be investigated. This trial will provide a new basis for oncologically feasible, safe and effective new surgical technique for mediastinal lymph node dissection in patients with early lung cancer undergoing minimally invasive surgery. Furthermore, the preventive effect of vagus nerve preservation on incidence of chronic cough will be objectively be proven and thus help to broaden the current knowledge of the role of vagus nerve and postoperative chronic cough.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Vagus Nerve Injuries, Cough

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
214 patients will be divided into two groups. Control group (N=107): Effort to preserve the pulmonary branch of vagus nerve preservation is not made in this group during mediastinal lymph node dissection Treatment group (N=107): Effort to preserve the pulmonary branch of vagus nerve preservation is made in this group during mediastinal lymph node dissection
Masking
None (Open Label)
Allocation
Randomized
Enrollment
214 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pulmonary branch of vagus nerve preserved
Arm Type
Experimental
Arm Description
Pulmonary branch of vagus nerve is preserved during the mediastinal lymph node dissection using minimally invasive surgery
Arm Title
Pulmonary branch of vagus nerve not-preserved
Arm Type
Experimental
Arm Description
Pulmonary branch of vagus nerve is not preserved during the mediastinal lymph node dissection using minimally invasive surgery
Intervention Type
Procedure
Intervention Name(s)
Pulmonary branch of vagus nerve preserved
Intervention Description
During the mediastinal lymph node dissection using minimally invasive surgery, efforts to preserve the pulmonary branch of vagus nerve is made.
Intervention Type
Procedure
Intervention Name(s)
Pulmonary branch of vagus nerve not preserved
Intervention Description
During the mediastinal lymph node dissection using minimally invasive surgery, efforts to preserve the pulmonary branch of vagus nerve is not made/ can be severed.
Primary Outcome Measure Information:
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Preoperative day
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Postoperative day (discharge day, an average of 1 week)
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Postoperative 1 month follow up at outpatient clinic
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Postoperative 2 month follow up at outpatient clinic
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Postoperative 6 month follow up at outpatient clinic
Title
Qualitative measurement of postoperative cough
Description
Cough Visual Analog Scale (VAS) will be used for survey. The Cough VAS is a numeric scale from 0-10 scale, with 0 indicating that patient experiences no distress from cough and 10 indicating severe distress from cough.
Time Frame
Postoperative 12 month follow up at outpatient clinic
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Preoperative day
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Postoperative day (discharge day, an average of 1 week)
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Postoperative 1 month follow up at outpatient clinic
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Postoperative 2 month follow up at outpatient clinic
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Postoperative 6 month follow up at outpatient clinic
Title
Quantitative measurement of postoperative cough
Description
The Korean version of the Leicester Cough Questionnaire will be used for survey. Comparison of preoperative and and postoperative change in objective cough frequency and quality of life among patients using the Leicester Cough Questionnaire, which is a 7 point Likert scale with a minimum value of 1 indicating chronic cough impacts participant life all of the time and a maximum value of 7 indicating chronic cough impacts participant life none of the time.
Time Frame
Postoperative 12 month follow up at outpatient clinic
Secondary Outcome Measure Information:
Title
Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Description
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Time Frame
Preoperative day
Title
Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Description
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Time Frame
Postoperative 1 day
Title
Serum TRPA1, TRPV1, bradykinin, PGE2 measurements
Description
Measurement of TRPA1 (ng/mL), TRPV1 (ng/mL), bradykinin (pg/mL), PGE2 (pg/mL) (released from C-fibers) via enzyme-linked immunosorbent assay (ELISA) test to quantitatively measure the injures of the vagus nerve during the mediastinal lymph node dissection.
Time Frame
Postoperative 2 month follow up at outpatient clinic
Title
Pulmonary function test
Description
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Time Frame
Preoperative day
Title
Pulmonary function test
Description
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Time Frame
Postoperative 1 month follow up at outpatient clinic
Title
Pulmonary function test
Description
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Time Frame
Postoperative 2 month follow up at outpatient clinic
Title
Pulmonary function test
Description
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Time Frame
Postoperative 6 month follow up at outpatient clinic
Title
Pulmonary function test
Description
Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function
Time Frame
Postoperative 12 month follow up at outpatient clinic
Title
Incidence of postoperative pulmonary complications, hospital stay and readmission, ICU care
Time Frame
from admission for operation to until the date of first documented postoperative complication or readmission, whichever came first), assessed up to 30 days
Title
Histopathologic review of the total number of mediastinal lymph node dissected
Description
Total number of dissected mediastinal lymph nodes and metastatic lymph nodes will be analyzed. Patient's preoperative clinical N stage and pathologic N stage will be compared; if pathologic N stage is higher than that of the clinical N stage, it will be considered as nodal upstaging.
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects clearly understand the purpose of the study, are willing and able to comply with the requirements to complete the study, and can sign the informed consent. Clinically suspicious of non-small cell lung cancer or tissue confirmed preoperatively Clinical stage T1-3/N0-1/M0 Preoperative ECOG performance status 0-1 Preoperative ASA class I-III Preoperative pulmonary function test FEV1 ≥ 60%, DLCO ≥ 60% Patients expected to achieve R0 (complete resection) via simple lobectomy and mediastinal lymph node dissection Exclusion Criteria: Patients who smoked within 2 weeks prior to operation Patients who received antitussives and expectorants 2 weeks prior to operation Patients who are pregnant or breast feeding Patients with severe or uncontrolled psychological disorders Patients with severe pulmonary adhesion Patients who are ineligible for minimally invasive surgery; thoracotomy conversion Patients diagnosed with other malignancies within 2 years prior to operation Patients who received chemotherapy or radiotherapy within 6 months prior to operation Patients suspicious of clinical N2 or received neoadjuvant therapy prior to operation Patients with cough-related diseases; COPD, asthma, ILD, GERD Patients suspicious of lymph node metastasis/invasion around vagus nerve during the preoperative clinical staging evaluation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kwhanmien Kim, MD. PhD
Phone
+82-31-787-7130
Email
kmkim0070@snubh.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kwhanmien Kim, MD. PhD
Organizational Affiliation
Department of Thoracic and Cardiovascular Surgery, Seoul National University Bundang Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Seoul National University
City
Seongnam-si
State/Province
Bundang
ZIP/Postal Code
13620
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Beatrice C Shih, MD
Phone
821091094533
Email
82430@snubh.org
First Name & Middle Initial & Last Name & Degree
Kwhanmien Kim, MD.PhD.

12. IPD Sharing Statement

Plan to Share IPD
No
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Citation
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Vagus Nerve Preservation and Chronic Cough in Non-small Cell Lung Cancer Surgery

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