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An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance

R

Robin, Alan L., M.D.

Status and phase

Completed
Phase 4

Conditions

Glaucoma
Ocular Hypertension

Treatments

Drug: travoprost, latanoprost, or bimatoprost
Drug: Additional ocular hypotensive medication

Study type

Interventional

Identifiers

NCT00329095
GMED-01

Details and patient eligibility

About

This is an open-label study in patients who are currently using either a topical prostaglandin as sole ocular hypotensive medical therapy q.d., or a topical prostaglandin plus an adjunctive topical ocular hypotensive marketed product either q.d., or b.i.d. in the same eye(s). Compliance will be measured over the two months of participation.

Full description

This is an open-label study in patients who are currently using either a topical prostaglandin as sole ocular hypotensive medical therapy q.d., or a topical prostaglandin plus an adjunctive topical ocular hypotensive marketed product either q.d., or b.i.d. in the same eye(s). Compliance will be measured over the two months of participation.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Currently using one or two topical ocular hypotensive medications

Exclusion criteria

  • Hypersensitivity to any component of medication

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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