Bioavailability of Bimatoprost Ophthalmic Solution in Human Aqueous.

ClinicalTrials.gov ID: NCT00355446

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Official title

Bioavailabilty of Bimatoprost Ophthalmic Solution in Human Aqueous.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assay human aqueous for bimatoprost and the presence of any metabolites, especially prostaglandin analogs. Hypothesis:Bimatoprost is not metabolized to a prostaglandin F-2-alpha analog in human eyes * Bimatoprost levels in human aqueous peak approximately three hours post dosing

Study identification

NCT ID: NCT00355446
Recruitment status: Completed
Study type: Interventional
Phase: Phase 4
Lead sponsor: Indiana University; Other
Enrollment: 48 participants

Conditions and interventions

Conditions

Cataract

Interventions

Bimatoprost 0.03% Drug

Drug

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jul 2001 (Type not available)
Primary completion: Not listed
Completion: Oct 2004 (Type not available)
Last update posted: Oct 17, 2007

2001 – 2004

United States locations

U.S. sites: 4
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
University Hospital	Indianapolis	Indiana	46202	—
Veterans Affairs Medical Center	Indianapolis	Indiana	46202	—
Wishard Memorial Hospital	Indianapolis	Indiana	46202	—
IU Eye at Carmel	Indianapolis	Indiana	46290	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00355446, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Oct 17, 2007 · Synced Nov 15, 2026