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AstigamtismNCT01121861

Prospective Comparative Study of Refractive Outcome of STAAR and Alcon Toric Intraocular Lenses

A study testing Phacoemulsification with implantation of toric IOL in people with Astigamtism, run by Singapore National Eye Centre at 1 site in Singapore.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Several methods have been developed to address and reduce preexisting astigmatism. The refractive results associated with the use of toric IOLs are likely to be more predictable. Read more about this study

Who is it for?
Ages 21 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Astigamtism
What is being tested?
Phacoemulsification with implantation of toric IOL
Type of treatment
Surgery or procedure
How many people
100 participants
Where
1 siteSingapore
Study dates
Jun 2007to Nov 2009
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 21 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Suitability for phacoemulsification surgery.
  • Regular corneal astigmatism of at least 1.25D and not exceeding 2.0D.
  • Age range between 21-80 years.
  • Informed consent of surgery and implantation of toric IOL obtained.

Who cannot join

  • Presence of irregular corneal astigmatism.
  • Regular corneal astigmatism less than 1.0D.
  • Presence of other ocular diseases that may compromise on the visual outcome such as glaucoma, retinal diseases, macular diseases and corneal diseases.

Trial locations and contacts

1 site in 1 country.

Singapore1 site
  • Singapore National Eye Centre

    Singapore, 168751

Other trials in Singapore

About this study

Official title: Prospective Comparative Study of the Efficacy, Predictability, Safety and Stability of the STAAR and Alcon Toric Intraocular Lenses Implanted in Asian Eyes During Phacoemulsification Surgery

Several methods have been developed to address and reduce preexisting astigmatism. The refractive results associated with the use of toric IOLs are likely to be more predictable. Other advantages of toric IOL include absence of need for any additional astigmatic correction procedure during cataract surgery, faster visual recovery as well as the reversibility of the procedure. There has not been any trial carried out to evaluate the results of toric IOL in either the investigators local population or in East Asia. Hence, the investigators set out to evaluate and compare the efficacy, safety, predictability and stability of the STAAR and Alcon toric IOL in Asian eyes.

Read the detailed description

The improvements in surgical technique as well as advances in technology employed during modern cataract surgery have made it a safe procedure in routine cases. Moving forwards, the single most pressing challenge facing cataract surgeons in the developed countries today is the ability to achieve predictable and accurate refractive outcomes. Increasingly, surgeons and patients alike have come to measure the success of their surgery by the refractive outcome.

Using partial coherence interferometry has led to more accurate biometry and consequently more predictable spherical results. This also helped paved the way for satisfactory correction of presbyopia with multifocal intraocular lenses (IOL).

Astigmatism is also an important component of the refractive equation. Estimates of the incidence of significant, naturally occurring astigmatism vary widely from 7.5% to 75%1. It is thought that 3% to 15% of eyes may have 2 or more diopters (D) of astigmatism2. Many surgeons would agree that astigmatism of greater than 0.5 D will have visual consequences such as symptoms of ghosting and shadows and they now aim for both spherical and astigmatic outcomes of +/ - 0.5 D3.

Several methods have been developed to address and reduce preexisting astigmatism. While corneal relaxing incisions for astigmatic correction can be unpredictable and highly surgeon dependent, the opposite is true for toric IOLs. The refractive results associated with the use of toric IOLs are likely to be more predictable as it is independent of corneal wound healing. The implantation of an IOL is also less surgeon dependent. Other advantages associated with toric IOLs include the absence of need for any additional astigmatic correction procedure during cataract surgery, faster visual recovery as well as the reversibility of the procedure.

Studies have been carried out to evaluate the efficacy and rotational stability of the STAAR AA4203 TF/TL toric IOL since its FDA approval in November 1998. These trials have only been carried out on Caucasian eyes and have shown a significant reduction in the pre-existing refractive astigmatism, improvement of postoperative unaided visual acuity as well as excellent refractive as well as rotational stability (latter especially so with the TL model). Ruhswurm et al.6 reviewed 37 eyes with STAAR toric IOL over a mean duration of 20.3 months and found that 78.4% of eyes had residual refractive astigmatism within +/- 1.00 D and 48.6% within +/- 0.50D. 83.4% of these eyes achieved best-corrected visual acuity of 20/40 or better. Sun et al.7 demonstrated improved unaided visual outcome between eyes with toric (130 eyes; 86.4% with visual acuity 20/40 or better) and spherical IOL (51 eyes; 76% with visual acuity 20/40 or better). Similar results have also been obtained with the Alcon toric IOL. In Horn et al.9, the clinical trial results of 250 patients with Alcon toric IOL have been described, demonstrating good unaided visual acuity of 20/25 or better at the 6-month postoperative visit (66% of patients with unilateral toric implant and 97% with bilateral implants). 97% of these toric patients achieved spectacle freedom for distance vision, compared to 50% of control patients. It is well documented that the rotational stability of these toric IOL is crucial to the efficacy of astigmatic reduction. Theoretical calculations show that an estimated 1/3 of astigmatic correction is lost if the IOL is rotated by 10 degrees off axis, as well as potential worsening of preoperative astigmatism in the presence of more than 30 degrees of off-axis rotation. Toric IOL stability is dependent on multiple factors, one of which is the capsular bag size. Vass et al.11 showed a good correlation between axial length and capsular bag diameter (CBD), especially so in eyes with axial lengths of less than 25.0mm. On the other hand, highly myopic eyes are not shown to have a greater risk of having a larger CBD than those with normal axial lengths. A formula derived to calculate a predicted CBD (CBDp) showed that values greater than 10.3mm are likely to have existing larger CBD and hence benefit from implantation of longer toric IOL due to better centration.

To date, there has not been any trial carried out to evaluate the results of toric IOL in either our local population or in East Asia. There has also not been any prospective clinical trial conducted to compare the difference (if any) between a plate-haptic and loop-haptic toric IOL. Hence, we set out to evaluate and compare the efficacy, safety, predictability and stability of the STAAR and Alcon toric IOL in Asian eyes.

Conditions
Astigamtism
Being tested
Phacoemulsification with implantation of toric IOL
Keywords
efficacy, safety, predictability, stability, toric IOL, refractive astigmatism, phacoemulsification

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Phacoemulsification with implantation of toric IOLProcedure or surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Amount of astigmatism reduction

    Measured: 3 months

Secondary outcomes (1)
  1. Stability of toric IOL

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 May 2010 (estimated)
  2. Study startJun 2007
  3. Primary completionNov 2009
  4. Study completionNov 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01121861
Sponsor's protocol ID
R536/24/2007
Status last verified
May 2010
First submitted
10 May 2010
Last updated
12 May 2010
Results posted
No
Data monitoring committee
No

Publications

  • Horn JD. Status of toric intraocular lenses. Curr Opin Ophthalmol. 2007 Feb;18(1):58-61. doi: 10.1097/ICU.0b013e328011f9bf.

    PubMed 17159449
  • Till JS, Yoder PR Jr, Wilcox TK, Spielman JL. Toric intraocular lens implantation: 100 consecutive cases. J Cataract Refract Surg. 2002 Feb;28(2):295-301. doi: 10.1016/s0886-3350(01)01035-5.

    PubMed 11821213
  • Chang DF. Early rotational stability of the longer Staar toric intraocular lens: fifty consecutive cases. J Cataract Refract Surg. 2003 May;29(5):935-40. doi: 10.1016/s0886-3350(02)01843-6.

    PubMed 12781279
  • Sun XY, Vicary D, Montgomery P, Griffiths M. Toric intraocular lenses for correcting astigmatism in 130 eyes. Ophthalmology. 2000 Sep;107(9):1776-81; discussion 1781-2. doi: 10.1016/s0161-6420(00)00266-9.

    PubMed 10964844
  • Patel CK, Ormonde S, Rosen PH, Bron AJ. Postoperative intraocular lens rotation: a randomized comparison of plate and loop haptic implants. Ophthalmology. 1999 Nov;106(11):2190-5; discussion 2196. doi: 10.1016/S0161-6420(99)90504-3.

    PubMed 10571358

Questions about this trial

What is this clinical trial studying?

A study testing Phacoemulsification with implantation of toric IOL in people with Astigamtism, run by Singapore National Eye Centre at 1 site in Singapore.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 May 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Amount of astigmatism reduction (time frame: 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01121861, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2010.

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