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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04806256
Other study ID # 2020-4-40915
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 11, 2020
Est. completion date December 2022

Study information

Verified date March 2021
Source Peking University Third Hospital
Contact Liyuan Tao, PhD
Phone +8610-82265571
Email tendytly@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project is based on artificial intelligence (AI) algorithms to screen the effective methods of traditional Chinese medicine intervention for dry eye and its applicable conditions, and optimize the traditional Chinese medicine intervention plan for dry eye through the evaluation of evidence-based medicine and expert consensus, and construct the Clinical Decision support system of traditional Chinese medicine intervention for dry eye, secondly, a real-world prospective cohort study design is adopted, the CDSS system is used in the ophthalmology clinic, and its practical application effect on patients with dry eye is evaluated.


Description:

Dry eye is a common disease that affects tears and ocular surface. It can cause ocular surface discomfort, visual impairment and even blindness, affect the quality of life of patients and cause social and psychological harm. Interventions related to traditional Chinese medicine can effectively alleviate the clinical symptoms and signs of patients with dry eye, and are an indispensable part of the treatment of dry eye. However, at present, patients with dry eye are mainly diagnosed at the western medicine ophthalmology clinic. Due to the lack of knowledge of Chinese medicine by western medicine ophthalmologists, they are unable to provide patients with good guidance on Chinese medicine intervention measures, which may cause patients to miss Chinese medicine-related treatments. This project provides doctors of Western medicine with a clinical decision support system (CDSS) of Chinese medicine interventions for dry eye syndrome, so as to improve doctors' guidance and decision-making of Chinese medicine for patients. This project is based on artificial intelligence (AI) algorithms to screen the effective methods of traditional Chinese medicine intervention for dry eye and its applicable conditions, and optimize the traditional Chinese medicine intervention plan for dry eye through the evaluation of evidence-based medicine and expert consensus, and construct the Clinical Decision support system of traditional Chinese medicine intervention for dry eye, secondly, a real-world prospective cohort study design is adopted, the CDSS system is used in the ophthalmology clinic, and its practical application effect on patients with dry eye is evaluated.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date December 2022
Est. primary completion date March 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Ages 18 to 80 year-old. 2. Meet the diagnostic criteria for dry eye, including ocular surface symptoms and signs. Exclusion Criteria: 1. There are contradictions in diagnostic information, and the real condition of the disease is doubtful; 2. The absence of necessary observation indicators; 3. Lack of necessary prognostic information; 4. The informed consent is not approved.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Clinical Decision Support System
This project is based on the artificial intelligence (AI) algorithm to screen the effective methods of traditional Chinese medicine intervention for dry eye and its applicable conditions, and optimize the traditional Chinese medicine intervention plan for dry eye through the evaluation of evidence-based medicine and expert consensus, and construct the traditional Chinese medicine intervention Clinical Decision Support Systems (CDSS) for dry eye. At the same time, the CDSS is provided to clinicians for their selection.
Other:
Routine intervention
The routine intervention without CDSS is also the clinically common intervention at present.

Locations

Country Name City State
China Peking University Third Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ocular Surface Disease Index Ocular Surface Disease Index (OSDI) is a potential useful instrument for the assessment of vision. Change from Before OSDI at 12 months after treatment
Primary Meibomain Gland Scale Meibomian gland function score (MGFS) is used to evaluate the function of the meibomian glands and whether there is meibomian gland dysfunction. Change from Before MGFS at 12 months after treatment
Secondary Tear Meniscus Height Tear Meniscus Height (TMH) refers to the level of tear fluid at the junction of the light band on the surface of the cornea and conjunctiva and the light band on the lower eyelid margin. Change from Before TMH at 12 months after treatment
Secondary Tear Break up time Tear Break up time (TBUT) is usually used to diagnose dry eye syndrome. Diluted fluorescein sodium liquid is instilled into the conjunctival fornix of the lower eyelid, and the patient is instructed to blink and hold it, and start timing. The time when the first rupture spot appears is the tear film rupture time. Change from Before TBUT at 12 months after treatment
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