Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01130974 · ClinicalTrials.gov registry record · NA

A Study to Assess the Safety and Efficacy of a Daily Disposable Contact Lens

A NA study, sponsored by Bausch & Lomb Incorporated.

Completed
Registry status
NA
Development phase
200
Enrollment target

NCT01130974: Completed NA study, sponsored by Bausch & Lomb Incorporated.

NCT01130974 is a NA study that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01130974, a NA study, has completed, sponsored by Bausch & Lomb Incorporated.

COMPLETED
Registry status
NA
Development phase
200 participants
Enrollment target

Study Summary

The objective of this study is to evaluate the safety and efficacy of the Bausch \& Lomb daily disposable tint contact lens (Test) compared to a currently marketed daily disposable cosmetic tint contact lens (Control).

Primary Outcome

Graded Slit lamp findings (epithelial edema, epithelial microcysts, corneal staining, limbal injection, bulbar injection, upper lid tarsal conjunctival abnormalities, corneal neovascularization, and corneal infiltrates) \> grade 2 over all follow-up visits, summarizes the worst case over all follow-up visits. Graded 0-4 with 0=none and 4=severe

Interventions

  • DEVICE Bausch & Lomb contact lens
  • DEVICE Marketed daily disposable contact lens

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2010-04
Est. Completion 2010-09
Phase NA
Bausch & Lomb Incorporated

174 total trials

What the finished NCT01130974 record still lists

NCT01130974 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower).

The record links to 0 conditions, and to 2 interventions - of which Bausch & Lomb contact lens is the first listed.

NCT01130974 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01130974 about?

NCT01130974 is a clinical study titled "A Study to Assess the Safety and Efficacy of a Daily Disposable Contact Lens". The objective of this study is to evaluate the safety and efficacy of the Bausch \& Lomb daily disposable tint contact lens (Test) compared to a currently marketed daily disposable cosmetic tint contact lens (Control).

What is the current status of trial NCT01130974?

This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2010-04. Estimated completion is 2010-09.

What interventions are being tested in trial NCT01130974?

The interventions under investigation include: Bausch & Lomb contact lens (DEVICE), Marketed daily disposable contact lens (DEVICE).

Who is sponsoring clinical trial NCT01130974?

This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01130974's enrollment target sits among peer trials

200 506th of 2000 higher than 1,434 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00107289 · 200 participants · Phase 2

    Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma

  • NCT00109174 · 200 participants · NA

    MRS Measurement of Glutamate and GABA Metabolism in Brain

  • NCT00177268 · 200 participants

    Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research

  • NCT00493688 · 200 participants

    A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01130974, the US trial registry maintained by the National Library of Medicine. NCT01130974 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.