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Exploration of Pupil Dilation in Horner's Patients Taking Flomax

D

Denver Health and Hospital Authority

Status and phase

Terminated
Phase 4

Conditions

Horner Syndrome

Treatments

Drug: 10% phenylephrine

Study type

Interventional

Funder types

Other

Identifiers

NCT03615508
COMIRB 18-0620

Details and patient eligibility

About

This study is evaluating the pupil dilation of Horner's Patients who have ever taken an alpha blocker such as Tamsulosin. Patients will undergo eye dilation as would occur at a yearly eye examination, but their pupil dilation measurements will be recorded.

Full description

This study will enroll 10 participants who have a unilateral Horner's Syndrome AND have a history of taking an alpha blocker such as Tamsulosin. Participants will be recruited based on those two enrollment criteria, and after consenting they will undergo pupil dilation with 10% phenylephrine. Once fully dilated the pupil size will be measured. Pupil dilation size of the eye affected by the Horner's Syndrome will be compared to the eye not affected by Horner's. Primary study outcome is the comparative dilation size of the Horner's affected eye to the non affected eye in all subjects.

Enrollment

1 patient

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Horner's Syndrome
  2. History of taking an alpha blocker (tamsulosin/ terazosin/doxazosin/alfuzosin/silodosin) medication

Exclusion criteria

  1. Subjects with untreated hypertension
  2. Subjects with thyrotoxicosis
  3. Pregnant women
  4. Prisoners
  5. Inability to consent
  6. Subjects with anatomical narrow angles who have never had a dilated exam

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1 participants in 1 patient group

10% phenylephrine
Other group
Description:
All patients will receive 10% phenylephrine at their eye examination as the drug to dilate the pupil. After pupil dilation, pupil size will be measured.
Treatment:
Drug: 10% phenylephrine

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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