Clinical trial registry record

A Phase Ⅱ Clinical Study of Sanhuangjingshimingwan in Wet( Neovascular)Age-related Macular Degeneration(wAMD) Subjects

A registered PHASE2 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Completed.
Evidence
Registered phase 2 study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated November 25, 2022.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT04486963
Last registry update
November 25, 2022
Status
Completed
Phase
Phase 2
Sponsor
Tasly Pharmaceutical Group Co., Ltd
Enrollment
78
Countries
China
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered PHASE2 study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase 2
Study design
RANDOMIZED · PARALLEL · TREATMENT · QUADRUPLE
Evidence population
Human clinical study registration
Participants
78
Population
ALL · 50 Years to 80 Years
Duration
2020-07-24 to 2022-11-15
Intervention
Sanhuangjingshimingwan; Sanhuangjingshimingwan Placebo
Comparator
Sanhuangjingshimingwan Placebo group
Outcomes measured
The average number of reinjections — at week 24; The percentage of subjects in both arms receiving reinjection of Anti-VEGF injection — at screening;at week 4;at week 8…; The average number of days between the second injection and baseline injection — at screening;at week 4;at week 8;at we…; Change from baseline in BCVA — at screening;at week 4;at week 8;at week 12;at week 16;at week 20;at week 24; The BCVA increasing >5, >10 and > 15 letters change from baseline — at screening;at week 4;at week 8;at week 12;at week…; The BCVA decreasing<5, <10 and < 15 letters change form baseline — at screening;at week 4;at week 8;at week 12;at week…; The BCVA decreasing≥15, ≥30 letters change form baseline — at week 24; Change from Baseline in Central Retinal Thickness (CRT) — at screening;at week 4;at week 8;at week 12;at week 16;at wee…; Change from Baseline in Choroidal Neovascularization (CNV) area — at screening;at week 4;at week 8;at week 12;at week 1…; Change from Baseline in leakage area — at week 24; Change from Baseline in the number of polypoid choroidal vasculopathy(PCV) and Branching vascular network(BVN) area — a…; Change from Baseline in TCM(Traditional Chinese Medicine) syndrome scores — at screening;at week 4;at week 8;at week 12…; Change from Baseline in the effective TCM syndrome scores — at screening;at week 4;at week 8;at week 12;at week 16;at w…
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase 2A trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Vision ageing · 100%Title contains controlled term: age-related macular degeneration. Source terminology contains: age-related macular degeneration. Title supplies longevity context: age-related. Study type is explicitly identified as INTERVENTIONAL.

Automated source check 100% · update recency 50%. These figures help sort records; they are not medical ratings.