Skip to content

Evaluation of the effect of Hab-alZahab ( Daymolax) on glaucoma symptoms

The explanation of Glaucoma in Persian medicine and evaluation of the effect of Hab-alZahab drug on Intraocular pressure and symptoms of glaucoumatos patients, compared with commonly prescribed drugs ( Latanoprost ,Timolol ,Dorzolamide)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190624043994N1
Enrollment
68
Registered
2021-08-18
Start date
2021-08-06
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Glaucoma. Glaucoma

Interventions

Intervention 1: Intervention group:Hab_AlZahab ( daymolex ) produced by Daymond pharmaceutical company ? a500 mg tablet every night, for 4 weeks. Intervention 2: Control group: Placebo tablet produ

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 85 years old, Diagnosed with Chronic Glaucoma, Signed Written Informed Consent Form, Capable of Cooperation and Responding to Questions.

Exclusion criteria

Exclusion criteria: Allergy to Aleovera Chronic Systemic Diseases : Uncontrolled Hypertension Cardiac disease? Gastrointestinal (GI) disease , Malignancy , Abdominal Pain with Unknown Cause , Obstructive and Inflammatory Bowel Disease , Acute Glaucoma , Ophthalmic Surgery , Pregnancy , Breast Feeding , Taking Corticosteroids ,Diuretics and .Thiazids Drugs.

Design outcomes

Primary

MeasureTime frame
Intraocular pressure. Timepoint: 0,1,2,4 weeks after intervention. Method of measurement: Slit lamps.

Secondary

MeasureTime frame
Headache. Timepoint: Before intervention and 7,14,21 days after intervention. Method of measurement: ?Asking.;Abdominal pain. Timepoint: Before intervention and 7,14.21 days after intervention. Method of measurement: Asking.;Diarrhea. Timepoint: Before intervention and 7,14.21 days after intervention. Method of measurement: Asking.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAssie Jokar

Mazandaran University of Medical Sciences

e.heydari@mazums.ac.ir+98 11 3324 4893

Outcome results

None listed

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