Skip to content

To study the effect and safety of Forskolin eye drops 1% in patients suffering from Open angle Glaucoma

To assess the efficacy and safety of Forskolin eye drops 1% in cases of Open angle Glaucoma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/12/004188
Enrollment
90
Registered
2013-12-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Adult male or female subjects with primary open angle glaucoma

Interventions

Intervention1: Forskolin eye drops 1%: Two drops three times a day for 28 days Control Intervention1: Nil: Nil

Sponsors

Sami labs Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Adult patients male or female having open angle glaucoma will be included in the study 2 Glaucoma with intra ocular pressure of more than 24 mm/Hg will be included. 3 No miotic or other therapy 24 hours before 4 off systemic therapy for glaucoma for at least 4 days 5 Informed consent given

Exclusion criteria

Exclusion criteria: 1 Inflammatory ophthalmic dose during the last 3 months 2 Secondary or closed angle glaucoma 3 Bronchial asthma 4 Chronic obstructive pulmonary disease 5 Uncompensated cardiac failure 6 Sinus bradycardia 7 2nd or 3rd degree AV Block 8 Concurrent drug intake for eg β blockers diamox etc 9 Pregnant women

Design outcomes

Primary

MeasureTime frame
Efficacy of Forskolin eye drops 1%Timepoint: Reduction in Intra ocular pressure as compared to Baseline. Tonometric readings will be recorded at 0.5,1,2,3,4,5 and 6 hours.

Secondary

MeasureTime frame
Safety of Forskolin eye drops 1%Timepoint: Adverse Events will be assessed at all visits - Day 1, Day 7, Day 14, Day 21 and Day 28.

Countries

India

Contacts

Public ContactMs Prachi Lad

ClinWorld(P)Limited

prachi@clinworld.org66981992

Outcome results

None listed

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