Multi-center Clinical Trial on Corneal Morphology Analysis in Chinese Population

Sponsor
Tianjin Eye Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03010748
Collaborator
Jilin University (Other), Health Science Center of Xi'an Jiaotong University (Other), Second People's Hospital of Yunnan Province (Other), Wuhan General Hospital of Guangzhou Military Command (Other), Xinjiang Medical University (Other), Gansu Provincial Hospital (Other)
50,000
1
49
1020.7

Study Details

Study Description

Brief Summary

Based on the corneal morphometry instrumentation Oculus Pentacam, which is commonly used before and after clinical refractive surgery, we will collect the corneal morphological and biologic parameters of the population under refractive surgery screening in refractive surgery centers around the country, and construct corneal morphology database in different living areas of Chinese people. Based on this, compared with the suspected keratoconus and keratoconus population, the screening criteria and reference standards accord with the characteristics of keratoconus of Chinese ethnic will be achieved.

Condition or Disease Intervention/Treatment Phase
  • Device: Scheimpflug tomography system (Pentacam) measurement

Detailed Description

The safety of refractive surgery has always been the focus of attention, keratoconus screening is the most important part for the preoperative examination of refractive surgery. Favorable tools and appropriate indicators are the premise of fast and accurate screening, and the corneal morphology from various regions of China have various characteristics, the use of uniform standards developed by foreign screening will always induce a lot of problems, for example, the differences of cornea morphological features between European and American ethnic and Chinese race, as well as the corneal morphometric indicators between various regions of China, will cause varying degrees of false-positive or false-negative screening results. Based on this, in order to further improve the safety of refractive surgery effectively and to obtain the effective and accurate screening of suspected keratoconus population, this study will be conducted to collect the corneal morphological characteristics database of Chinese people from all over the country, and to develop a database of Chinese ethnographic characteristics for screening keratoconus indicators and reference valuable to guide clinical screening and surgical design.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50000 participants
Observational Model:
Case-Crossover
Time Perspective:
Cross-Sectional
Official Title:
Multi-center Clinical Trial on Corneal Morphology Analysis in Chinese Population
Study Start Date :
Nov 1, 2015
Anticipated Primary Completion Date :
Aug 1, 2019
Anticipated Study Completion Date :
Dec 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Chinese population

Chinese population of different nation from several provinces.

Device: Scheimpflug tomography system (Pentacam) measurement
The Scheimpflug tomography system (Pentacam,Oculus GmbH, Wetzlar, Germany) is a rotating Scheimpflug camera that measures 138,000 true elevation points to compute corneal topography. Patients were asked to blink twice and then look at the fixation device. Image acquisition was a 2-second scan of 50 rotational Scheimpflug images through the corneal sighting point, the point where the ray of light from the fovea to the fixation device crossed the cornea. All measurements were performed just after a blink to minimize the effect of tear film alteration on the data. Acceptable maps had at least 10.0 mm of corneal coverage with no extrapolated data in the central 9.0 mm zone.

Outcome Measures

Primary Outcome Measures

  1. corneal thickness [preoperative]

Secondary Outcome Measures

  1. corneal curvature measured by the Pentacam system [preoperative]

  2. coma aberration measured by the Pentacam system [preoperative]

  3. aspherical index measured by the Pentacam system [preoperative]

  4. spherical aberration measured by the Pentacam system [preoperative]

  5. corrected distance visual acuity [preoperative]

  6. uncorrected distance visual acuity [preoperative]

  7. refractive diopter [preoperative]

  8. corneal volume measured by the Pentacam system [preoperative]

  9. kapple angle measured by the Pentacam system [preoperative]

  10. introcular pressure [preoperative]

  11. corneal diameter measured by the Pentacam system [preoperative]

  12. anterior chamber depth measured by the Pentacam system [preoperative]

  13. anterior chamber angle measured by the Pentacam system [preoperative]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • No less than 18 years old, in good health, have no active disease in the body and eye, have permanent resident status and have lived in the local area for at least 5 years (please mark the nation).
Exclusion Criteria:
  • Eye diseases, glaucoma, ocular hypertension, glaucoma patients with normal pressure, fundus lesions, ptosis and other eyelid abnormalities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tianjin Eye Hospital Tianjin China

Sponsors and Collaborators

  • Tianjin Eye Hospital
  • Jilin University
  • Health Science Center of Xi'an Jiaotong University
  • Second People's Hospital of Yunnan Province
  • Wuhan General Hospital of Guangzhou Military Command
  • Xinjiang Medical University
  • Gansu Provincial Hospital

Investigators

  • Study Director: Yan Wang, director, Tianjin Eye Hospital
  • Principal Investigator: Xiaoyu li, Second People's Hospital of Yunnan Province
  • Principal Investigator: Yan Zhang, Jilin University
  • Principal Investigator: Jun Yang, Gansu Provincial Hospital
  • Principal Investigator: Jing Li, Health Science Center of Xi'an Jiaotong University
  • Principal Investigator: Xianglong Yi, Xinjiang Medical University
  • Principal Investigator: Zhengwei Shen, Wuhan General Hospital of Guangzhou Military Command

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Tianjin Eye Hospital
ClinicalTrials.gov Identifier:
NCT03010748
Other Study ID Numbers:
  • Tianjin EH-pentacam
First Posted:
Jan 5, 2017
Last Update Posted:
May 4, 2018
Last Verified:
May 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Tianjin Eye Hospital

Study Results

No Results Posted as of May 4, 2018