Combined Capsular Tension Ring & IOL Implantation for Management of

Clinical Trial Summary

This study included cataract patients who underwent intraocular lens (IOL) implantation with or without capsular tension ring (CTR), which aimed to evaluate the contribution of the use of CTR in clinical visual outcomes and rotational stability of IOL after cataract surgery.

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT04226196` - Rotational Stability of a Hydrophobic Acrylic Plate Haptic Intraocular Lens Using a Capsular Tension Ring - An Intraindividual Comparative Study	N/A
	Recruiting	`NCT06294405` - Intraocular Lens Implant Registry Study

See also

Status

Clinical Trial

Phase

Recruiting

NCT04226196 - Rotational Stability of a Hydrophobic Acrylic Plate Haptic Intraocular Lens Using a Capsular Tension Ring - An Intraindividual Comparative Study

N/A

Recruiting

NCT06294405 - Intraocular Lens Implant Registry Study

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT05530473
Study type	Interventional
Source	Eye & ENT Hospital of Fudan University
Contact
Status	Completed
Phase	N/A
Start date	January 1, 2020
Completion date	March 30, 2023

Combined Capsular Tension Ring and IOL Implantation for Management of Cataracts

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms