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Evaluation of synergistic effect and relapse reduction of Jiajian Zhujingfang combined with Conbercept Opthalmic injection in the treatment of pathological myopia choroid neovascularization

Evaluation of synergistic effect and relapse reduction of Jiajian Zhujingfang combined with Conbercept Opthalmic injection in the treatment of pathological myopia choroid neovascularization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006435
Enrollment
Unknown
Registered
2022-08-04
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

pathological myopia

Interventions

test group:Intravitreal injection of Conbercept + Jiajian Zhujingfang Granules
control group:Intravitreal injection of Conbercept +placebo granules

Sponsors

Eye Hospital China of Academy Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ?At least one case meeting the above diagnostic criteria; ? TCM syndrome type is liver and kidney deficiency type; ?Age 18-60 years old (excluding 18 years old and 60 years old); ? Not receiving fundus laser or intrabulbar injection of anti-VEGF drugs within 3 months; ? The refractive interstitium is basically clear and does not hinder the fundus examination or fundus fluoroscopy examination; ? The subjects can understand and are willing to accept the treatment and re-examination according to the experimental plan; ? Sign the informed consent.

Exclusion criteria

Exclusion criteria: ?Combined age-related macular degeneration, glaucoma, diabetic retinopathy, retinal artery occlusion, retinal vein occlusion, idiopathic or secondary epimacular membrane, choroidopathy, optic nerve disease (optic neuritis, optic atrophy), macular hole, etc. eye disease that affects the outcome; ?The test eye has undergone intraocular surgery within 3 months; ? Those who have participated in clinical trials of any drug or medical device within 3 months before the trial, or those who plan to participate in other clinical trials during this trial; ? Those who are allergic to sodium fluorescein; ? Patients with moderate or severe liver dysfunction, or patients with severe heart, lung, kidney dysfunction, hematopoietic system diseases and mental illness; ? Those who cannot cooperate with the inspection process; ?Can not insist on tracking fundus examination; ? Pregnant and lactating patients; ? Participating in other clinical investigators.

Design outcomes

Primary

MeasureTime frame
best corrected visual acuity;

Secondary

MeasureTime frame
Recurrence rate;TCM symptom score;macular hemorrhage absorption;retinal thickness;Choroidal neovascular leakage;

Countries

China

Contacts

Public ContactZe-Feng Kang
zefeng2531@163.com13552597717

Outcome results

None listed

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