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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01169688
Other study ID # NWKSC_2007_01
Secondary ID
Status Completed
Phase N/A
First received July 22, 2010
Last updated July 22, 2010
Start date December 2007
Est. completion date April 2008

Study information

Verified date December 2007
Source Northwest Kansas Surgery Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study was done to compare efficacy, safety and efficiencies of various methods of pupil dilation prior to cataract surgery.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Ability to self administer eye or have a helper for the task of administering eye drops.

- Ability to follow and eye drop administration schedule.

- No noted ocular abnormalities.

- Bilateral cataract surgery anticipated.

Exclusion Criteria:

- Inability to self administer eye drops or have assistance with eye drop administration.

- Health problems that would contraindicate self administration of dilating eye drops such as poor cardiovascular or respiratory status.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms

  • Cataract
  • Mydriasis
  • Pupil Dilation Prior to Cataract Surgery In-patient
  • Pupil Dilation Prior to Cataract Surgery Out-patient

Intervention

Other:
Pupil dilation with phenylephrine 10% vs cyclopentolate 2%


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Northwest Kansas Surgery Center