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Real World Data Study Assessing The Persistency Of Xalacom And The Other Fixed Dose Combination Products, Duotrav And Ganfort, In The United Kingdom

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Viatris

Status

Completed

Conditions

Glaucoma
Ocular Hypertension

Treatments

Drug: Ganfort
Drug: Duotrav
Drug: XALACOM

Study type

Observational

Funder types

Industry

Identifiers

NCT01206361
A6111145

Details and patient eligibility

About

The hypothesis is that there is no difference in persistency between Xalacom and the alternative fixed dose combination products (Duotrav and Ganfort) over a 12 month period.

Enrollment

2,015 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who had received a prescription for either Xalacom, Ganfort and DuoTrav
  • Greater than 18 years old
  • Diagnosed with glaucoma or ocular hypertension
  • Registered at the primary care practice for > 12 months

Exclusion criteria

  • None

Trial design

2,015 participants in 1 patient group

fixed dose prostaglandin combination
Treatment:
Drug: Ganfort
Drug: Duotrav
Drug: XALACOM

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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