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Study of herbal drug of HESA-A on dry Age related Macular Degeneration

Comparison of herbal drug of HESA-A with placebo from the view point of their influence on visual acuity and side effects on patients suffering from dry Age related Macular Degeneration

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013091514667N1
Enrollment
60
Registered
2013-10-21
Start date
2008-12-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Dry age related macular degeneration. Senile Macular Degeneration( Atrophic)

Interventions

Intervention 1: HESA-A wil be available as coated pills (996 mg) from Osveh pharmaceutical company. Drug will be given to treatment group as 50 mg bid in the first month then it will be given a week
Treatment - Drugs
Placebo
HESA-A wil be available as coated pills (996 mg) from Osveh pharmaceutical company. Drug will be given to treatment group as 50 mg bid in the first month then it will be given a week in a month as ab
Placebo will be given to control group as coated pills from Osveh pharmaceutical company in the dose of 50 mg/kg bid in the first month then it will be given a week in a month as above dose.

Sponsors

Hamedan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are mild or moderate loss of vision due to AMD including: non-central atrophy, RPE changes, multiple intermediate drusens (64-124 microns) or one large drusen ( diameter more than 124 microns) at least in one eye. Exclusion criteria are Corrected visual acuity less than 20/200, CNV or presence of any other ocular disease except mild cataract (1+)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Corrected visual acuity. Timepoint: before intervention and every month. Method of measurement: snellen chart.

Secondary

MeasureTime frame
Choroidal neovascularization. Timepoint: before intervention and every month. Method of measurement: fluorescein angiography and OCT of retina.;Ophthalmic or systemic side effects. Timepoint: every month in follow up period. Method of measurement: examination with slit lamp, super field lens and goldman tonometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Bashirian

Hamedan university of medical sciences

vc_research@umsha.ac.ir+98 81 1838 0574

Outcome results

None listed

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