Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04676620
Other study ID # 2020-K-107
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 2020
Est. completion date December 2021

Study information

Verified date December 2020
Source Shanghai Guanghua Hospital of Integrated Traditional Chinese and Western Medicine
Contact Hongxia Wang, director
Phone 18302183233
Email whxeye@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Conductive keratoplasty (CK) had shown to be a safe and effective procedure for the treatment of low to moderate hypeopia. It had been approved by the U.S. Food and Drug Administration (FDA) to treat presbyope in early 2004. CK appeals to both surgeons and patients as it avoids the need for flap creation, the use of high intraocular pressure (IOP), or tissue ablation. It utilizes "blended vision" rather than the true monovision used with laser in situ keratomileusis (LASIK), which patients tolerate more readily. There is very little reported research about the induction of wavefront aberration by CK. The symptomatology of high order aberrations (HOA) and the way individual Zernike functions were correlated with visual acuity, contrast sensitivity, visual symptoms. This study measured the HOA created by surgically induced myopic shift via CK and LASIK in an effort to better understand the phenomena of regression, multifocality, pseudo-accommodation and monovision.


Description:

To investigate anterior corneal optical higher order aberration (HOA) induced by conductive keratoplasty (CK) and laser in situ keratomileusis (LASIK). 69 eyes with hyperopia or presbyopia were enrolled. 47 eyes of 47 patients underwent CK procedure, 22 eyes underwent LASIK. Data were acquired preoperatively, and at 3 and 6 months postoperatively. The total Root Mean Square (RMS) of the HOA as well as the individual Zernike polynomials of coma, trefoil, and spherical aberration were analyzed. In CK group, the high order RMS showed significant elevation at 3 months, but it returned to near preoperative levels at 6 months postoperatively. Trefoil (Z33) is the exclusive Zenike pattern to increase significantly following CK, peaking at 3 months and then decreasing back to near preoperative level at 6 months after CK. In the hyperopic LASIK group, coma increased to a peak at 3 month postoperatively, and persisted at sixth month after LASIK. Spherical aberration decreased significantly at 3 months and persisted till the sixth postoperative month. There was significant correlation between ΔSE and Δspherical aberration showed in both groups. The HOA and main Zernike polynomials pattern and their natural changes induced by CK is significantly different from that induced by LASIK in the hyperopic corrected treatment. The amount of achieved hyperopic corrections induced by CK or LASIK is not correlated to the change of HOA patterns such as coma and trefoil, but it is correlated to the change of spherical aberration.


Recruitment information / eligibility

Status Recruiting
Enrollment 69
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - age of over 40 years old (yrs) - stable refraction - planned to induce a myopic shift Exclusion Criteria: - age of less than 40 years old (yrs) - significant systemic illnesses - congenital myopia, - media opacity uveitis - glaucoma - intraocular surgery refractive surgery - neurologic diseases - retinal disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
CK surgery
CK and LASIK are both effective methods for the correction of hypeopia. They have been proved to offer many advantages in terms of visual acuity, corneal sensitivity, and corneal biomechanics compared with traditional refractive surgeries.

Locations

Country Name City State
China Shanghai Guanghua Integrated Traditional Chinese and Western Medicine Hospital Shanghai Shanghai

Sponsors (2)

Lead Sponsor Collaborator
Wang Hongxia Tianjin Eye Hospital

Country where clinical trial is conducted

China, 

References & Publications (3)

Du TT, Fan VC, Asbell PA. Conductive keratoplasty. Curr Opin Ophthalmol. 2007 Jul;18(4):334-7. Review. — View Citation

Lin DY, Manche EE. Two-year results of conductive keratoplasty for the correction of low to moderate hyperopia. J Cataract Refract Surg. 2003 Dec;29(12):2339-50. — View Citation

Pallikaris lG, Naoumidi TL, Panagopoulou SI, Alegakis AK, Astyrakakis NI. Conductive keratoplasty for low to moderate hyperopia: 1-year results. J Refract Surg. 2003 Sep-Oct;19(5):496-506. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary uncorrected visual acuity uncorrected visual acuity change from baseline at 6 months change from baseline with EDTRS chart at 6 months
Primary best spectacle-corrected visual acuity best spectacle-corrected visual acuity change from baseline with EDTRS chart at 6 months change from baseline with EDTRS chart at 6 months
Secondary near vision near vision change from baseline with EDTRS chart at 6 months change from baseline with EDTRS chart at 6 months
Secondary central and peripheral corneal ultrasound pachymetry central and peripheral corneal ultrasound pachymetry change from baseline with EDTRS chart at 6 months change from baseline with EDTRS chart at 6 months
See also
  Status Clinical Trial Phase
Recruiting NCT04075591 - Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects With Presbyopia N/A
Completed NCT03169153 - Clinical Comparison of Silicone Hydrogel Monthly Lenses N/A
Completed NCT02517567 - DAILIES TOTAL1® - Comparative Assessment of Tear Film Evaporation N/A
Recruiting NCT02844556 - International Multicenter Study on SMILE Surgery N/A
Completed NCT02214797 - Dispensing Study to Assess Visual Performance of Prototype Contact Lenses N/A
Completed NCT02235831 - DAILIES® AquaComfort Plus® Multifocal (MF) - Comparative Assessment of Visual Performance N/A
Completed NCT01917162 - Multi-Center Clinical Evaluation of Two Daily Disposable Contact Lenses (Study 2) N/A
Completed NCT01941498 - WaveLight® Refractive Myopic Study N/A
Completed NCT01629706 - Determination of Cell Population in Solution-Induced Corneal Staining (SICS) and Symptomatic Versus Asymptomatic Lens Wearers N/A
Completed NCT01440322 - AIR OPTIX® COLORS Registration Trial N/A
Completed NCT01211535 - Subjective Comfort With Multipurpose Care Solutions in Soft Contact Lens Wearers N/A
Completed NCT01233089 - Fitting Children With Contact Lenses N/A
Completed NCT01163760 - Clinical Evaluation of Two Daily Disposable Contact Lenses N/A
Completed NCT02484586 - Dispensing Study to Assess the Visual Performance of Optimised Prototype Contact Lenses N/A
Completed NCT02252133 - DAILIES TOTAL1® Lens Centration in a Japanese Population N/A
Completed NCT01941485 - WaveLight® Refractive Flap Accuracy Study N/A
Completed NCT02103309 - Comparative Evaluation of Contact Lens Centering of DAILIES® AquaComfort Plus® Versus 1-DAY ACUVUE® MOIST® in Japan N/A
Completed NCT01951573 - Evaluation of a New Daily Disposable Multifocal Contact Lens Design N/A
Recruiting NCT01718184 - Piggyback Sulcoflex Toric IOL for Correcting Refractive Error Following Corneal Transplantation N/A
Completed NCT01997216 - Multifocal Lens Design Evaluation N/A