- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05441202
Lung Nodule Intervention Cohort Study (LNICS)
June 28, 2022 updated by: Chinese Chronic Respiratory Disease Research Network
The Efficacy of Transdermal Therapy for Lung nodule---an Real Word Observational Study
Incident lung nodule is quite common in China.
The major treatment method is long-term floolow up without a specific intervention.
We aim to investigate the efficacy an safty of a novel transdermal therapy with Chinese herb.
The study included two arms: one arm is routine treatment and another arm is routine treatment plus transdermal therapy.
The study end point is the change of lung nodule size under CT scan.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: xiaohong liu, MD
- Phone Number: +8618364166279
- Email: 18364166279@163.com
Study Contact Backup
- Name: Guangxi Li
- Email: li.guangxi@mayo.edu
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100053
- Recruiting
- Guang An Men Hospital
-
Contact:
- XIAOHONG LIU, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
any patient with incident lung nodule after health check up
Description
Inclusion Criteria:
- incident lung nodule patients
Exclusion Criteria:
- severe baseline conditions
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change of lung nodule size
Time Frame: three months minimal
|
change of lung nodule size before and after intervention
|
three months minimal
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 1, 2022
Primary Completion (ANTICIPATED)
July 31, 2022
Study Completion (ANTICIPATED)
January 1, 2025
Study Registration Dates
First Submitted
June 28, 2022
First Submitted That Met QC Criteria
June 28, 2022
First Posted (ACTUAL)
July 1, 2022
Study Record Updates
Last Update Posted (ACTUAL)
July 1, 2022
Last Update Submitted That Met QC Criteria
June 28, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- LN002
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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