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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ChiCTR |
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Last refreshed on:
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11 September 2017 |
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Main ID: |
ChiCTR-INR-17012623 |
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Date of registration:
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2017-09-08 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Clinical evaluation of different femtosecond laser fragmentation patterns of the nucleus in cataract surgery
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Scientific title:
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Clinical evaluation of different femtosecond laser fragmentation patterns of the nucleus in cataract surgery |
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Date of first enrolment:
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2017-09-11 |
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Target sample size:
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1:60;2:60;3:60; |
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Recruitment status: |
Recruiting |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=20895 |
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Study type:
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Interventional study |
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Study design:
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Randomized parallel controlled trial
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Phase:
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New Treatment Measure Clinical Study
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Countries of recruitment
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China
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Contacts
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Name:
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Ke Yao
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Address:
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88 Jiefang Road, Hangzhou, Zhejiang, China
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Telephone:
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+86 13906517262 |
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Email:
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xlren@zju.edu.cn |
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Affiliation:
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Eye Center of Second Affiliated hospital of Zhejiang University School of Medicine |
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Name:
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Zeren Shen
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Address:
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88 Jiefang Road, Hangzhou, Zhejiang, China
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Telephone:
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+86 13732229034 |
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Email:
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zrshen@zju.edu.cn |
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Affiliation:
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Eye Center of Second Affiliated hospital of Zhejiang University School of Medicine |
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Key inclusion & exclusion criteria
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Inclusion criteria: Male or female patients, 18-90 years of age, with cataract were enrolled. Patients were schedule to undergo femtosecond laser-assisted cataract surgery.
Exclusion criteria: Excluded were patients with allergy to any of the study medications, corneal diseases or ocular infectious disease, history of ocular chemical or thermal burn or any ocular operation, glaucoma or ocular hypertension, history of serious systemic disease, or other conditions that in the opinion of the investigator precluded enrollment. Patients who were initially included were excluded if they had intraoperative or postoperative complications. Women who were pregnant or lactating were not permitted to be in the study.
Age minimum:
18
Age maximum:
90
Gender:
Both
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Health Condition(s) or Problem(s) studied
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cataract
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Intervention(s)
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1:4-segments Chop Mode;2:6-segments Chop Mode;3:Frag Mode;
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Primary Outcome(s)
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IOP;UDVA;CDVA;endothelial cell density;central corneal thickness;
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Source(s) of Monetary Support
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N/A
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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