Medical Information Only. Consult your healthcare provider before considering clinical trial enrollment.

ClinicalTrials.gov 22 recruiting now later-stage tilt

Myopia: later-stage trial registry

22 of 91 indexed Myopia trials are currently recruiting, with more weight in Phase 3-4.

Corpus placement: #151 of 28,707 conditions by registered trial count.

91 US clinical trials · 22 currently recruiting · #151 of 28,707 conditions by registered trial count

Myopia: 91 US clinical trials tracked, 22 recruiting.

Myopia is the subject of 91 registered US clinical trials on ClinicalTrials.gov, 22 of them currently open to new participants. 4 are in Phase 3-4 (later-stage) and 2 in Phase 1-2 (earlier-stage). The most active sponsor is CooperVision, running 13 of these trials.

Enrollment posture brief

Registry condition myopia

OPEN 22 | RECR 24% | LATE 4 | EARLY 2 | RANK #151 | SPON 13

Nearest open-share peer: HIV/AIDS (24% recruiting · 62 trials)

Cerebral Palsy48.9%Critical Illness44.6%Sepsis36.3%Metastatic Melanoma34.8%Myopia (this)24%
Open-enrollment share among volume-matched conditions near Myopia

Myopia lists 22 open slots (24% of 91 indexed trials). Peers are matched on registered volume, not therapeutic-area browse lists. How peer matching works →

Key findings

What ClinicalTrials.gov does not surface for Myopia on its own pages , computed from the registry mirror as of 2026-08-08. Each line carries its own denominator so it can be quoted as it stands.

  1. Myopia is recruiting below its size-band peers.

    22 of 91 indexed trials (24.2%) are open to enrollment, against a 39.7% average across 762 conditions with 20-99 trials. The peer set uses the same ClinicalTrials.gov-derived counts as this page.

  2. Sponsorship of Myopia trials is spread across many organizations.

    CooperVision accounts for 13 of 91 trials (14.3%). 44 distinct sponsors appear on at least one study for this condition label.

  3. Typical Myopia enrolment sits around 80 participants.

    Median target enrolment is 80 among the 91 trials that report a genuine target (sentinel values excluded). 51 of those (56%) plan for fewer than 100 participants.

  4. Myopia research is mostly interventional.

    78 interventional and 13 observational studies make up this index (85.7% interventional). Study type is sponsor-reported on ClinicalTrials.gov.

Phase 22Phase 31Phase 43

Open and recent trials

91 total, page 2 of 2

COMPLETED NA 173 participants

Safety and Efficacy of a Contact Lens for Daily Disposable Use

Bausch & Lomb Incorporated

NCT01365039

COMPLETED NA 159 participants

Myopia Control With a Innovative Spectacle Lens

Essilor International

NCT05174780

COMPLETED NA 118 participants

DAILIES TOTAL1 Versus ACUVUE TruEye - Effects on the Biology of the Ocular Surface and Lid Margin

University of Texas Southwestern Medical Center

NCT02347631

COMPLETED NA 114 participants

A Multi-Center Investigation of Patient Acceptability of OPTI-FREE RepleniSH® Multi-Purpose Disinfecting Solution (MPDS)

Alcon Research

NCT00772707

COMPLETED NA 112 participants

Clinical Performance of Two Commercial, Daily Disposable Contact Lenses

Alcon Research

NCT05010512

COMPLETED NA 109 participants

Comparative In-Vivo Wetting Characteristics of Silicone Hydrogel Materials With Selected Lens Care Systems

Alcon Research

NCT01699750

COMPLETED 108 participants

Air Optix Night and Day Aqua (AONDA) Retrospective Study 1

Alcon Research

NCT05790928

COMPLETED NA 107 participants

DD T2 Daily Disposable Registration Trial

Alcon Research

NCT03305770

COMPLETED NA 100 participants

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens

Bausch & Lomb Incorporated

NCT01412983

COMPLETED NA 90 participants

Clinical Evaluation of Stenfilcon A Soft Contact Lens When Compared to Ocufilcon B Soft Contact Lens

CooperVision

NCT01354223

COMPLETED NA 90 participants

Multi-Center Clinical Evaluation of Two Reusable Soft Contact Lenses

CooperVision

NCT02542072

COMPLETED NA 85 participants

Study of Theories About Myopia Progression (STAMP)

Ohio State University

NCT00335049

COMPLETED NA 79 participants

Comparison of Two Daily Disposable Lenses

Alcon Research

NCT04013789

COMPLETED NA 77 participants

Clinical Evaluation of Reusable Soft Contact Lenses

CooperVision International Limited (CVIL)

NCT06119191

COMPLETED NA 69 participants

Performance Evaluation of Daily Disposable Contact Lenses in Habitual Lens Wearers Who Use Digital Devices Frequently

CooperVision

NCT05805150

COMPLETED NA 66 participants

A Study to Evaluate a New Silicone Hydrogel Contact Lens

Bausch & Lomb Incorporated

NCT01309893

COMPLETED NA 66 participants

Evaluation of a New Silicone Hydrogel Contact Lens

Bausch & Lomb Incorporated

NCT01309880

COMPLETED NA 66 participants

Clinical Assessment of a Daily Wear Monthly Replacement Soft Silicone Hydrogel Contact Lens

Alcon Research

NCT04476784

COMPLETED NA 64 participants

Performance Comparison Between Fanfilcon A and Senofilcon A Sphere Lenses

CooperVision

NCT02956460

COMPLETED NA 63 participants

A Study to Evaluate the Product Performance of the PureVision®2 High Definition (HD) Contact Lens

Bausch & Lomb Incorporated

NCT01416142

COMPLETED 61 participants

An Outcomes Study Comparing the Intralase FS 60 to the Intralase iFS When Performing LASIK Surgery for Nearsightedness

Stanford University

NCT01365728

COMPLETED 58 participants

A Dispensing Clinical Trial of Test Contact Lens Against Marketed Contact Lens

CooperVision

NCT03499067

COMPLETED NA 53 participants

Performance Evaluation of Reusable Contact Lenses When Worn For One Month By Habitual Soft Contact Lens Wearers

CooperVision

NCT06098339

COMPLETED NA 52 participants

A Dispensing Comparison of a Test Daily 1 Day Lens Against a Control 1 Day Lens.

CooperVision

NCT03951610

COMPLETED Phase 4 51 participants

Effect of Preoperative Pupil Size on Quality of Vision After Wavefront-Guided LASIK

Stanford University

NCT00889941

COMPLETED NA 51 participants

IntraLase vs Hansatome Flaps in LASIK

Stanford University

NCT00691431

COMPLETED NA 50 participants

Patient Satisfaction With Contoura Vision Topography-Guided LASIK

Rush Eye Associates

NCT04903301

COMPLETED 50 participants

Patient Reported Satisfaction With Contoura LASIK Utilizing the Phorcides Analytic Software

Mann Eye Institute

NCT05848817

COMPLETED NA 50 participants

Apioc Contact Lens Feasibility

Lentechs

NCT03688672

COMPLETED NA 50 participants

A Prospective Evaluation of Contrast Sensitivity and Disability Glare in Refractive Surgery, a Sub-Study of: Initial Evaluation of Excimer Laser Keratorefractive Surgery in U.S. Army Personnel (WU # 2335-99)

Walter Reed Army Medical Center

NCT00413868

COMPLETED NA 50 participants

Vistakon Investigational Lens Worn as a Single Use Daily Wear

Johnson & Johnson Vision Care

NCT01031004

COMPLETED 49 participants

Quality of Vision and Quality of Life With LASIK

Edward E. Manche

NCT02161263

COMPLETED NA 45 participants

A One-Week Crossover Dispensing Evaluation of New Daily Wear Soft Contact Lenses

CooperVision

NCT03306641

COMPLETED NA 44 participants

Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)

University of Utah

NCT00713856

COMPLETED Phase 2 35 participants

Cannabinoid vs Opioid for Photorefractive Keratectomy Pain Control

University of Florida

NCT05477875

COMPLETED 35 participants

Clinical Validation of the Apollo Daily Disposable Soft Contact Lenses

CooperVision

NCT05035017

COMPLETED Phase 4 32 participants

The Influence of Atropine on Choroidal Thickness

State University of New York College of Optometry

NCT03158142

COMPLETED NA 31 participants

A 6-Hour Clinical Evaluation of New Daily-Wear Soft Contact Lenses

CooperVision

NCT03235089

COMPLETED 20 participants

Bromday Versus Nevanac Eye Drops to Control Pain Following Photorefractive Keratectomy

Virdi Eye Clinic

NCT01475877

COMPLETED NA 18 participants

A Contralateral Dispensing Clinical Trial of Study Test Sapphire Lens Against Enfilcon A Silicone Hydrogel Lens

CooperVision

NCT02518490

COMPLETED NA 10 participants

Dynamic Change in Accommodation After Wearing Multifocal Soft Contact Lenses for Myopia Control

State University of New York College of Optometry

NCT04763694

← Previous Page 2 of 2

Phase Distribution

PhaseTrial count
Phase 2 2
Phase 3 1
Phase 4 3

Named interventions

Most-linked intervention names on Myopia records (sponsor-reported on ClinicalTrials.gov). Counts are trial links, not unique products.

senofilcon A Device
3 trials
Test lens Device
3 trials
LASIK Procedure
3 trials
Spectacle lenses Device
3 trials
Novel spectacle lens design Device
3 trials
nelfilcon A contact lens Device
2 trials
Control Lens Device
2 trials
Test Lens Device
2 trials

US sites by state

Facility locations filed on Myopia trials. A trial with sites in several states counts in each.

California 36 trials
Florida 26 trials
Texas 23 trials
New York 23 trials
Ohio 19 trials
Kansas 14 trials
Illinois 14 trials
Tennessee 12 trials

Source: ClinicalTrials.gov, National Library of Medicine. Data is informational only.

What to do with this Myopia page

91 registered trials, 22 currently recruiting, is a starting point for a conversation, not a diagnosis or a recommendation.

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This Myopia condition card totals 91 registered trials; most-linked intervention senofilcon A; top US site state California. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.