AzTrials
AzTrials

CataractsNCT01867541

Intra-operative Measurements to Predict the Position of the Intraocular Lens Post-operatively

An observational study of Cataracts, run by Prim. Prof. Dr. Oliver Findl, MBA.

Completed

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

Official record
Search all trials

Trial summary

Refractive outcome after cataract surgery mainly depends on the prediction of the intraocular lens that is implanted in the eye during surgery. Aim of this study is to measure the position of the lens capsule during surgery and to use this measurements to improve post-operative refractive outcomes. Read more about this study

Who is it for?
Ages 21 years and older
Conditions the study is for
Cataracts
How many people
70 participants
Where
No sites listed yet
Study dates
Dec 2010to Mar 2013
Phase
Observational
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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: patients who are sceduled for cataract surgery

Who may be able to join

  • Cataract
  • Age 21 and older
  • written informed consent prior to surgery

Who cannot join

  • Relevant other ophthalmic diseases such as: pseudoexfoliation, glaucoma, traumatic cataract, corneal scars, and other co-morbidity
  • In case of pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)

About this study

Official title: Predictability of the IOL Position Using an Intra-operative OCT

Refractive outcome after cataract surgery mainly depends on the prediction of the intraocular lens that is implanted in the eye during surgery.

Aim of this study is to measure the position of the lens capsule during surgery and to use this measurements to improve post-operative refractive outcomes.

Read the detailed description

During the last decades the refractive outcome after cataract surgery improved significantly.

The total prediction error in IOL power calculation (and therefore in the refractive outcome) can be divided into 3 main parameters:

  • Axial eye length (in mm)
  • Corneal power (in dioptres)
  • Estimation of post-operative anterior chamber depth (ACD) (in mm)

Since the introduction of optical biometry (IOLMaster, Carl Zeiss Meditec AG, Jena, Germany), as a reliable non-contact measurement of the axial eye length the influence of the error of axial length measurement on the refractive error decreased from over 50% (when measured with applanation ultrasound) to 36%. The mean error of corneal power measurement is approximately 22%.

These results show that the estimation of the post-operative intra-ocular lens (IOL) position and therefore the estimated anterior chamber depth (ACD) is nowadays the main source of error (35%to 42%) in IOL power calculation and therefore for the refractive outcome of the patients after cataract surgery.

Early IOL power calculation formulas, such as the Binkhorst I formula, used a fixed ACD value to predict the position of the IOL, but the refractive results were not appropriate, because the post-operative position of the IOL varied significantly between patients. Later observations showed a correlation between the axial eye length and the post-operative ACD (longer=more myopic eyes showed a larger ACD post-operatively). These correlations were taken into account in later developed formulas (such as the Binkhorst II formula).

Olsen et al. measured the post-operative ACD and substituted the predicted post-operative ACD with the true, post-operative ACD in each case. The result after correcting the IOL position was a highly accurate IOL power calculation, where no fudge factors were needed.

Nowadays the pre-operatively measured ACD is taken into account for several IOL power calculation formulas, such as the Haigis formula, the Holladay II formula and the Olsen formula.

However, this new generation of formulas uses the pre-operative ACD, without considering the thickness of the crystalline lens. The ACD is measured as the distance between the anterior surface of the cornea (anatomically correct would be the posterior surface of the cornea, but in an optical context, as in IOL power calculations, the anterior surface is used) and the anterior surface of the crystalline lens . Therefore the thickness of the crystalline lens has a significant impact on the predicted post-operative position of the IOL. This parameter was first taken into account by Olsen and later modified by Norrby.

It should be mentioned that IOL power calculations developed from theoretical calculations based on Gaussian optics to regression formulas, such as the SRK formula 11 that uses retrospective data of a large number of patients. Nowadays ray tracing is available that uses a numerical solution to calculate the IOL power.

All these findings suggest that a proper measurement of the position and the size of the crystalline lens as well as of the lens capsule after removing the crystalline lens is necessary to improve IOL power calculation.

Recently a device was introduced that allows measurements of the crystalline lens as well as the lens capsule itself after removing the crystalline lens of cataract patients intra-operatively. This device uses optical coherence tomography (OCT) technology to create high resolution B-scans (=images) of the anterior segment of the eye. The OCT was shown to be highly reproducible for ACD measurements pre-operatively and small changes of the IOL/crystalline lens can be detected.

The intra-operative OCT may allow measurements of the crystalline lens, of the lens capsule and furthermore of the position of the IOL intra-operatively. Therefore it may be possible for the first time, to directly observe the correlation of the position and size of the crystalline lens to the IOL position intra-operatively.

Number of subjects In total, 50 eyes of 50 subjects will be included.

  • Standard eyes (IOL power 18 - 23 D): 30 eyes
  • Long (myopic) eyes (IOL power < 18 D) - 10 eyes
  • Short (hyperopic) eyes (IOL power > 23 D) - 10 eyes

Study Visits On the day of pre-operative examination, the patient will undergo a full ophthalmic assessment and routine biometry will be performed for axial length measurement and Keratometry (IOLMaster, Carl Zeiss Meditec AG, Jena, Germany). Furthermore pre-operatively the ACD and lens thickness (LT) will be measured (ACMaster, Carl Zeiss Meditec AG, Jena, Germany).

Surgery is performed in topical anaesthesia. The standard preoperative therapy is tropicamide 1% gtt, phenylephrine 2.5% gtt, cyclopentolate 1% gtt. An on-axis self-sealing incision, injection of viscoelastic substance, capsulorhexis, phacoemulsification, irrigation/aspiration of cortical material are performed as standard procedure. After measurement, the IOL will be implanted using the dedicated injector system.

Intra-operative study-related measurements:

OCT scans will be performed at 4 different stages intra-operatively:

  1. At the beginning of the surgery
  2. After removing the natural crystalline lens with phakoemulsification and irrigation/aspiration (I/A). The infusion handpiece of the I/A set (that is used routinely) will be placed into the paracentesis and the bottle height will be adjusted to control the pressure in the anterior chamber. It will be set to result in an estimated pressure of approximately 20mmHg. Therefore a hydraulic table with memory function will be used that can be set at exactly the same height for each patient and the infusion bottle will be placed at a height of 27cm above the eye (27.2cmH2O = 20mmHg). Then an OCT scan will be performed.
  3. Then ophthalmic viscosurgical device (OVD) is inserted and a capsular tension ring (CTR) will be implanted. Therefore the OVD is irrigated and aspirated and the measurement repeated.
  4. Afterwards the IOL is implanted and the viscoelastic is removed.

Outcome variables

Main outcome variable:

  • Intra-operative posterior capsule position with CTR in place Additional outcome variable
  • Posterior capsule position in phakic eyes
  • Posterior capsule position intra-operatively without CTR
  • Comparison of posterior capsule position of eyes with different axial eye length
Conditions
Cataracts
Keywords
cataract surgery, intraocular lens power calculation, effective lens position, improving the refractive outcome after cataract surgery, predicting the IOL position
Medical subject headings
Cataract

What is being measured

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

  1. Correlation of intra-operative lens capsule measurements and the post-operative lens position

    Aim of this outcome parameter is to detect, if intra-operative measurements (with an optical coherence tomogrophy system) help to detect the position of the artificial lens post-operatively

    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 posted4 Jun 2013 (estimated)
  2. Study startDec 2010
  3. Primary completionDec 2012
  4. Study completionMar 2013

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01867541
Sponsor's protocol ID
intraOP_OCT_1
Status last verified
May 2013
First submitted
26 May 2013
Last updated
4 Jun 2013
Results posted
No
Data monitoring committee
No

Publications

  • Hirnschall N, Amir-Asgari S, Maedel S, Findl O. Predicting the postoperative intraocular lens position using continuous intraoperative optical coherence tomography measurements. Invest Ophthalmol Vis Sci. 2013 Aug 5;54(8):5196-203. doi: 10.1167/iovs.13-11991.

    PubMed 23761092

Questions about this trial

What is this clinical trial studying?

An observational study of Cataracts, run by Prim. Prof. Dr. Oliver Findl, MBA.

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 3 inclusion and 2 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 4 Jun 2013. Status can change between updates, so confirm with the study contact before making plans.

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?

Correlation of intra-operative lens capsule measurements and the post-operative lens position (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 NCT01867541, which also lists 1 linked publication.

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 4 Jun 2013.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in