To Evaluate the Short-term and Long Term Efficacy of Acupuncture in Ocular and Oral Dryness Symptoms of Dry Eye Syndrome

NCT04877483 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2022-12-13

No results posted yet for this study

Summary

This study wants to use a randomized, single-blind, controlled trial to evaluate the efficacy of receiving acupuncture GB20 or GB20 plus BL2 on alleviating the ocular dryness symptom from dry eye syndrome and Sjögren's syndrome. One hundred dry eye syndrome subjects are composed of 50 dry eye syndrome subjects and 50 Sjögren's syndrome' dry eye subjects, and all are randomized into 40 Group GB20 and 40 Group GB20 plus BL2 (GBL), and 20 Group Waiting list; while we also include 20 healthy controls. Fifty dry eye syndrome subjects are randomized into 20 Group GB20, 20 Group GBL and 10 Group Waiting list in first year; while both Group GB20 or GBL received acupuncture twice a week 8 weeks for efficacy evaluation, and 10 Group Waiting list receive no any acupuncture treatment. And we could use the Whole-genome genotyping, oral microbiota, Schirmer's test, Tear breakup time, Cytokines, OSDI, TCM pattern, Traditional Chinese Medicine (TCM) tongue diagnosis, TCM pulse diagnosis, and TCM heart rate variability for this purpose. In second year, another 50 dry eye syndrome subjects are also enrolled and randomized into randomized into 20 Group GB20, 20 Group GBL and 10 Group Waiting list; while both Group GB20 or GBL received acupuncture twice a week 8 weeks for efficacy evaluation with above outcome measurements, and 10 Group Waiting list receive no any acupuncture treatment. Meanwhile, we also include 20 healthy controls, and we want to find the difference with the comparison between the dry eye syndrome, Sjögren's syndrome and healthy control in second year. Through the analysis for dry eye syndrome and Sjögren's syndrome, we could find the biomarker to differentiate dry eye syndrome, Sjögren's syndrome and healthy control. In the future, this work could be applied for screening and diagnosis of pre-dry eye syndrome and Sjögren's syndrome, and this integrated TCM with Western Medicine plan could be applied for the goal of holistic health care.

Conditions

  • Dry Eye Syndrome
  • Xerophthalmia

Interventions

PROCEDURE

Acupuncture

Acupuncture is a form of treatment that inserting very thin needles through a person's skin at specific points on the body. Group GB20 and Group GB20 plus BL2 will received the acupuncture treatment.

DIAGNOSTIC_TEST

Oral microbiota

Group GB20, Group GB20 plus BL2 and Healthy control will take the oral microbiota analysis.

DIAGNOSTIC_TEST

Schirmer's test

Group GB20 and Group GB20 plus BL2 will take the Schirmer's test.

DIAGNOSTIC_TEST

Tear breakup time

Group GB20 and Group GB20 plus BL2 will take the tear breakup time test.

DIAGNOSTIC_TEST

OSDI(Ocular Surface Disease Index)

Group GB20 and Group GB20 plus BL2 will take the OSDI test.

DIAGNOSTIC_TEST

TCM pattern

Group GB20, Group GB20 plus BL2 and Healthy control will take the Traditional Chinese Medicine pattern diagnosis.

DIAGNOSTIC_TEST

Traditional Chinese Medicine (TCM) tongue diagnosis

Group GB20, Group GB20 plus BL2 and Healthy control will take the Traditional Chinese Medicine(TCM) tongue diagnosis.

DIAGNOSTIC_TEST

TCM pulse diagnosis

Group GB20, Group GB20 plus BL2 and Healthy control will take the Traditional Chinese Medicine(TCM) pulse diagnosis.

DIAGNOSTIC_TEST

TCM heart rate variability

Group GB20, Group GB20 plus BL2 and Healthy control will take the TCM Heart rate variability.

DIAGNOSTIC_TEST

ESSPRI(EULAR Sjögren's Syndrome Patient Reported Index)

Group GB20 and Group GB20 plus BL2 will take the ESSPRI.

DIAGNOSTIC_TEST

Whole-genome genotyping(TWBv2.0)

Group GB20, Group GB20 plus BL2 and Healthy control will take the Whole-genome genotyping(TWBv2.0).

DIAGNOSTIC_TEST

Cytokine markers

Group GB20, Group GB20 plus BL2 and Healthy control will take the cytokine markers(IL-17、MMP-9、BAFF、BCMA) analysis.

DIAGNOSTIC_TEST

Blood biochemical analysis

Group GB20 and Group GB20 plus BL2 will take the Blood biochemical analysis(BUN,Cre,AST,ALT,ESR and CRP).

DIAGNOSTIC_TEST

complete blood count (CBC)

Group GB20 and Group GB20 plus BL2 will take the CBC(WBC、RBC、Hb、Platelet) analysis.

DIAGNOSTIC_TEST

SF-36(36-Item Short Form Survey )

Group GB20 and Group GB20 plus BL2 will take the SF-36 test.

Sponsors & Collaborators

  • Taipei Veterans General Hospital, Taiwan

    lead OTHER_GOV

Principal Investigators

  • Chang Ching-Mao, M.D., Ph.D. · Taipei Veterans General Hospital, Taiwan

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-06
Primary Completion
2022-12-31
Completion
2024-12-31

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04877483 on ClinicalTrials.gov