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Clinical Trials/NCT05453721
NCT05453721CompletedNot Applicable

Effect and Long-Term Outcomes of Indocyanine Green Fluorescence Imaging Method Versus Modified Inflation-Deflation Method in Identification of Intersegmental Plane: A Multicenter、Prospective、Randomized Controlled Trial

The First Affiliated Hospital of Nanchang University1 site in 1 country272 target enrollmentStarted: August 4, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
272
Locations
1
Primary Endpoint
Success rate of intersegmental plane identification

Study Overview

Brief Summary

This study is a multi-center, prospective, randomized controlled clinical trial. The purpose is to compare the difference of indocyanine green fluorescence imaging method and modified inflation-deflation method in identifying intersegmental plane in segmentectomy, and provide high-level evidence for the selection of intersegmental plane identification method in early NSCLC segmental resection.

Detailed Description

In patients with early-stage lung cancer, segmentectomy has comparable long-term survival results compared with conventional lobectomy, but patients have a higher postoperative quality of life because more lung tissue is preserved.

Segmentectomy is based on accurate anatomy, and the identification of intersegmental plane is one of the keys to accurate anatomy of segmentectomy.

At present, differential ventilation and differential colorimetry are clinically used to cause the difference between the target segment and the adjacent lung segment to identify intersegmental plane, which both have advantages and disadvantages. Clinical consensus on the best method for intersegmental plane identification has not been formed.

This study is a multi-center, prospective, randomized controlled clinical trial. The study plans to enroll 272 patients with peripheral stage I NSCLC with tumor diameter ≤2cm and consolidation tumor rate <1. Eligible patients will be randomly divided into the experimental group (indocyanine green fluorescence imaging method) or control group (modified inflation-deflation method) at a ratio of 1:1.

This study is expected to compare the difference of indocyanine green fluorescence imaging method and modified inflation-deflation method in identifying intersegmental plane in segmentectomy, and provide high-level evidence for the selection of intersegmental plane identification method in early NSCLC segmentectomy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 18 to 80 years old;
  • According to the surgical standards of the Eighth edition of People's Medical Publishing House, patients whose blood pressure was under 160/100mmHg and blood glucose was under 5.6-11.2mmol /L with normal functions of major organs such as heart, lung, liver and kidney before surgery are included. The main criteria are as follows:
  • i. Cardiac function examination indicated Goldman index grade 1-2; ii. Pulmonary function examination suggested postoperative predicted FEV1≥40% and DLCO≥40%; iii. Total bilirubin ≤1.5 times the upper limit of normal; iv. Alanine aminotransferase and aspartate aminotransferase ≤2.5 times the upper limit of normal value; v. Creatinine ≤1.25 times the upper limit of normal value and creatinine clearance ≥60ml/min;
  • The center of the lesion is located in the other lobes except the middle lobe, and in the middle and outer third of the lung;
  • The maximum diameter of the tumor was not more than 2cm on TLC(Thin layer CT) scan and the clinical stage was cT1a-1bN0M0(according to AJCC staging criteria, eighth edition);
  • Consolidation tumor rate <1;
  • ECOG PSscore 0-1;
  • All relevant examinations should be completed within 28 days before surgery;
  • Patients who understand the study and have signed informed consent.

Exclusion Criteria

  • Patient with a history of iodine or indocyanine green allergy;
  • Patient who had received antitumor therapy (radiotherapy, chemotherapy, targeted therapy, immunotherapy) prior to surgery;
  • Patient with a history of other malignancies;
  • Patient with secondary primary cancer at enrollment;
  • Small cell lung cancer;
  • Prior history of unilateral thoracotomy;
  • Woman in pregnant or breastfeeding period;
  • Patient with interstitial pneumonia, pulmonary fibrosis or severe emphysema;
  • An active bacterial or fungal infection that is difficult to control;
  • Severe mental illness;
  • History of severe heart disease , heart failure , myocardial infarction or angina pectoris within the last 6 months;
  • patient that researcher considers inappropriate to participate in this study.

Arms & Interventions

Indocyanine green fluorescence imaging method group

Experimental

Using indocyanine green fluorescence imaging method to identify intersegmental plane in segmentectomy

Intervention: Indocyanine green fluorescence imaging method (Procedure)

Modified inflation-deflation method group

Active Comparator

Using modified inflation-deflation method to identify intersegmental plane in segmentectomy

Intervention: Modified inflation-deflation method (Procedure)

Outcomes

Primary Outcomes

Success rate of intersegmental plane identification

Time Frame: During the operation

Successful intraoperative appearance of the intersegmental plane is considered a success

Secondary Outcomes

  • Intersegment plane identification time(During the surgery)
  • Surgery time(During the surgery)
  • Intraoperatve blood loss(During the surgery)
  • Postoperative blood loss(Postoperative in-hospital stay up to 30 days)
  • Postoperative air leakage rate(Postoperative in-hospital stay up to 30 days)
  • Quality of life(EORTCQLQ-C30)(6/12 months after surgery)
  • Postoperative 30-day mortality(Within 30 days after surgery)
  • Postoperative air leakage time(Postoperative in-hospital stay up to 30 days)
  • Adverse event level(Through study completion, an average of 2 year)
  • Adverse event rate(Through study completion, an average of 2 year)
  • Surgical complication(Postoperative in-hospital stay up to 30 days)
  • Postoperative 90-day mortality(Within 90 days after surgery)
  • Reoperation rate(Within 30 days after surgery)
  • Number of stapler nail bin used for cutting(During the surgery)
  • R0 resection rate(Within 14 days after surgery)
  • Postoperative pulmonary function(6/12 months after surgery)
  • Preoperative pulmonary function(1 week before the surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jian Tang

M.D., Ph.D, Professor

The First Affiliated Hospital of Nanchang University

Study Sites (1)

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