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Clinical study on the treatment of diabetic ischemic optic neuropathy with insulated body needles and low-power needling of the Shangjingming point and Qiuhou point

Clinical study on the treatment of diabetic ischemic optic neuropathy with insulated body needles and low-power needling of the Shangjingming point and Qiuhou point

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081173
Enrollment
Unknown
Registered
2024-02-26
Start date
2024-02-29
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Diabetic ischemic optic neuropathy

Interventions

Test group:The treatment of the primary disease+ Insulated body needles and low-power needling of the Shangjingming point and Qiuhou point
Control group:The treatment of the primary disease+ Conventional western medicine

Sponsors

Xiyuan Hospital of CACMS
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnosis of diabetic ischemic optic neuropathy. (2) Be between the ages of 45-75 years, (both 45 and 75 years) for both sexes. (3) Have not participated in any other clinical studies in the last 3 months. (4) Those who are informed about the study, sign the informed consent form, and voluntarily participate in and cooperate with the trial.

Exclusion criteria

Exclusion criteria: (1) Those who do not meet the diagnosis of diabetic ischemic optic neuropathy; (2) Those with broken skin at the site of acupuncture point extraction; (3) Those who have undergone fundus total retinal photocoagulation treatment; (4) Those who have combined glaucoma, serious diseases affecting the refractive system such as corneal disease, crystal dislocation, or serious fundus abnormalities such as acute fundus hemorrhage; (5) Combined with serious cardiac, cerebrovascular, hepatic and renal and other systemic diseases, long-term use of anticoagulant drugs and coagulation disorders; (6) Those who have a history of allergy to methylcobalamin, procaine and acupuncture needle metal; (7) Pregnant and lactating women; (8) Those who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity (BCVA);Visual field indicators;Optic disk blood flow ;

Secondary

MeasureTime frame
Intraocular pressure (IOP);Safety indicators;

Countries

China

Contacts

Public ContactLiqun Chu

Xiyuan Hospital of CACMS

chuliqunok@126.com+86 62835137

Outcome results

None listed

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