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Clinical Observation of Combined Acupuncture Points with Deep Puncture at the Acupoint Jingming BL1 for Glaucoma Treatment

Clinical Observation of Combined Acupuncture Points with Deep Puncture at the Acupoint Jingming BL1 for Glaucoma Treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028604
Enrollment
Unknown
Registered
2019-12-28
Start date
2020-02-03
Completion date
Unknown
Last updated
2020-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Interventions

Case series:deep puncture treatment

Sponsors

Jalan University, Malaysia
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Study participants will be those who are: 1. of either gender; 2. > 18 and < 80 years of age; 3. diagnosed as POAG according to the diagnostic criteria of POAG used in current ophthalmology practice; 4. not legally blind by the official definition of having central visual acuity of 20/200 or less in the better eye with corrective lenses, and /or a visual field of 20 degrees or less in the better eye; 5. never before treated with deep acupuncture at acupoint Jingming BL1 for glaucoma.

Exclusion criteria

Exclusion criteria: Exclusion criteria will be as follows: 1. Participants with cardiovascular, kidney, liver, or hematopoietic system diseases, mental health disorders, cancer or other severe diseases for whom acupuncture may be inappropriate or unsafe; 2. Participants with other diseases that could interfere with acupuncture treatment, e.g., clotting disorders or leukopenia, active skin infection, epilepsy, or on anticoagulant therapy (aspirin, warfarin etc); 3. Participants with a pacemaker, metal allergy, or severe fear of needles; 4. Women who are pregnant or lactating; 5. Participants who have difficulties in attending the trial (e.g. paralysis, cancer, dementia, drug addiction, time constraints, surgical operation).

Design outcomes

Primary

MeasureTime frame
Intraocular Pressure;

Countries

Malaysia

Contacts

Public ContactTe Kian Keong

Jalan University, Malaysia

tekk@utar.edu.my+60 1 62085808

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026