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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01480934
Other study ID # 01072007
Secondary ID
Status Completed
Phase N/A
First received November 24, 2011
Last updated November 28, 2011
Start date June 2005
Est. completion date June 2010

Study information

Verified date November 2011
Source Iladevi Cataract and IOL Research Center
Contact n/a
Is FDA regulated No
Health authority India: Institutional Review Board
Study type Observational

Clinical Trial Summary

To compare the development of posterior capsule opacification (PCO) between eyes with and without a history of diabetes mellitus (DM) after single-piece hydrophobic acrylic intraocular lens (IOL) implantation 4 years postoperatively.Diabetes mellitus would not increase the incidence of PCO at 4 years.


Description:

There is a paucity of available literature that prospectively evaluates the development of PCO with the single-piece hydrophobic acrylic IOL implantation in diabetic versus non-diabetic eyes on a long-term basis. Therefore, this study was designed to compare the degree of PCO after cataract surgery between diabetic and age-matched non-diabetic patients. This prospective, observational case control study comprised patients who underwent phacoemulsification .The patients were asked to return for postoperative follow-up visits at 1 month, 1 year and 4 years.

the digital images were analyzed for PCO .


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date June 2010
Est. primary completion date January 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

- Diabetes mellitus was defined as glycosylated haemoglobin (Hb A1c ) levels of 6% or more ,

- use of diabetic medication (oral hypoglycemic agents, insulin injection or diet restriction), or a physician's diagnosis of diabetes.

- Patients with uncomplicated age-related cataract who were otherwise healthy constituted the controls (n=75 eyes).

Exclusion Criteria:

- patients with glaucoma,

- high myopia (axial length > 27.0 mm),

- pseudoexfoliation,

- traumatic cataract,

- subluxated cataract,

- previous ocular surgeries,

- allergy to dilating drops.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Iladevi Cataract and IOL Research Center

Outcome

Type Measure Description Time frame Safety issue
Primary Development of Posterior capsule opacification. This prospective, observational case control study comprised patients who underwent phacoemulsification .Subjects with a history of diabetes mellitus (DM) were designated as cases (n=75 eyes).Inclusion criteria for cases: Diabetes mellitus was defined as glycosylated haemoglobin (Hb A1c ) levels of 6% or more , use of diabetic medication (oral hypoglycemic agents, insulin injection or diet restriction), or a physician's diagnosis of diabetes. Patients with uncomplicated age-related cataract who were otherwise healthy constituted the controls (n=75 eyes). 4 years No
Secondary duration of diabetes, stage of diabetic retinopathy The stage of diabetic retinopathy and duration of diabetes was correlated with the degree of PCO in the cases group. 4 years No