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

Sponsor
Seoul National University Bundang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04923412
Collaborator
(none)
214
1
2
12
17.9

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Pulmonary branch of vagus nerve preserved
  • Procedure: Pulmonary branch of vagus nerve not preserved
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
214 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention 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 dissection214 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)
Primary Purpose:
Treatment
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
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Jun 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pulmonary branch of vagus nerve preserved

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

Procedure: Pulmonary branch of vagus nerve preserved
During the mediastinal lymph node dissection using minimally invasive surgery, efforts to preserve the pulmonary branch of vagus nerve is made.

Experimental: Pulmonary branch of vagus nerve not-preserved

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

Procedure: Pulmonary branch of vagus nerve not preserved
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.

Outcome Measures

Primary Outcome Measures

  1. Qualitative measurement of postoperative cough [Preoperative day]

    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.

  2. Qualitative measurement of postoperative cough [Postoperative day (discharge day, an average of 1 week)]

    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.

  3. Qualitative measurement of postoperative cough [Postoperative 1 month follow up at outpatient clinic]

    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.

  4. Qualitative measurement of postoperative cough [Postoperative 2 month follow up at outpatient clinic]

    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.

  5. Qualitative measurement of postoperative cough [Postoperative 6 month follow up at outpatient clinic]

    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.

  6. Qualitative measurement of postoperative cough [Postoperative 12 month follow up at outpatient clinic]

    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.

  7. Quantitative measurement of postoperative cough [Preoperative day]

    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.

  8. Quantitative measurement of postoperative cough [Postoperative day (discharge day, an average of 1 week)]

    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.

  9. Quantitative measurement of postoperative cough [Postoperative 1 month follow up at outpatient clinic]

    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.

  10. Quantitative measurement of postoperative cough [Postoperative 2 month follow up at outpatient clinic]

    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.

  11. Quantitative measurement of postoperative cough [Postoperative 6 month follow up at outpatient clinic]

    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.

  12. Quantitative measurement of postoperative cough [Postoperative 12 month follow up at outpatient clinic]

    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

  1. Serum TRPA1, TRPV1, bradykinin, PGE2 measurements [Preoperative day]

    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.

  2. Serum TRPA1, TRPV1, bradykinin, PGE2 measurements [Postoperative 1 day]

    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.

  3. Serum TRPA1, TRPV1, bradykinin, PGE2 measurements [Postoperative 2 month follow up at outpatient clinic]

    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.

  4. Pulmonary function test [Preoperative day]

    Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function

  5. Pulmonary function test [Postoperative 1 month follow up at outpatient clinic]

    Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function

  6. Pulmonary function test [Postoperative 2 month follow up at outpatient clinic]

    Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function

  7. Pulmonary function test [Postoperative 6 month follow up at outpatient clinic]

    Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function

  8. Pulmonary function test [Postoperative 12 month follow up at outpatient clinic]

    Routine PFT (FEV1%, FEV1/FVC%) check to evaluate the effects of vagus nerve preservation in pulmonary function

  9. Incidence of postoperative pulmonary complications, hospital stay and readmission, ICU care [from admission for operation to until the date of first documented postoperative complication or readmission, whichever came first), assessed up to 30 days]

  10. Histopathologic review of the total number of mediastinal lymph node dissected [through study completion, an average of 1 year]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seoul National University Seongnam-si Bundang Korea, Republic of 13620

Sponsors and Collaborators

  • Seoul National University Bundang Hospital

Investigators

  • Study Director: Kwhanmien Kim, MD. PhD, Department of Thoracic and Cardiovascular Surgery, Seoul National University Bundang Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Kwhanmien Kim, Principal Investigator, Seoul National University Bundang Hospital
ClinicalTrials.gov Identifier:
NCT04923412
Other Study ID Numbers:
  • B-2007-625-007
First Posted:
Jun 11, 2021
Last Update Posted:
Sep 27, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 27, 2021