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Clinical Evaluation of Two Frequent Replacement Soft Spherical Contact Lenses

NCT05656885 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2023-12-27

Study results available
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Summary

This was a single-blind (participant masked), interventional, prospective, direct refit, bilateral wear short-term fitting study.

Conditions

  • Myopia
  • Hyperopia

Interventions

DEVICE

Lens A

Soft spherical hydrogel contact lens for 15 minutes

DEVICE

Lens B

Soft spherical silicone hydrogel contact lens for 15 minutes

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Juan G Carracedo Rodríguez, OD,MSc,PhD · University Complutense of Madrid

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-27
Primary Completion
2022-10-18
Completion
2022-10-18
FDA Device
Yes

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05656885 on ClinicalTrials.gov