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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06230393
Other study ID # DF6-CL-24-02
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date May 30, 2029

Study information

Verified date January 2024
Source New World Medical, Inc.
Contact Elysia Ison, OD
Phone 800 832 5327
Email eison@newworldmedical.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate long term safety and effectiveness of the STREAMLINE® SURGICAL SYSTEM


Description:

A Retrospective, nonrandomized, open-label study to evaluate the long term safety and IOP-lowering effectiveness of STREAMLINE® SURGICAL SYSTEM in patients with open-angle glaucoma who participated in the DF6-CL-20-01 protocol.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date May 30, 2029
Est. primary completion date April 30, 2029
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: participated in the DF6-CL-20-01 trial. Exclusion Criteria: lost to follow up in the DF6-CL-20-01 trial

Study Design


Intervention

Device:
STREAMLINE® SURGICAL SYSTEM
STREAMLINE® SURGICAL SYSTEM

Locations

Country Name City State
Costa Rica Clinica 20/20 San José

Sponsors (1)

Lead Sponsor Collaborator
New World Medical, Inc.

Country where clinical trial is conducted

Costa Rica, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in IOP From Screening to annual endpoints 24months; 36 months; 48months, 60 months
Secondary Number of IOP lowering medications Compared to screening in DF6-CL-20-01 trial 24months; 36 months; 48months, 60 months
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