Completed

Blepharospasm Patient Survey: A Structured Interview Evaluating Previous and Current incobotulinumtoxinA, abobotulinumtoxinA and onabotulinumtoxinA Treatment for Patients With Blepharospasm

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What is being collected

Data Collection

Other
Who is being recruted

Eye Diseases

+ Eyelid Diseases

+ Blepharospasm

From 18 to 81 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: September 2012
See protocol details

Summary

Principal SponsorMerz Pharmaceuticals GmbH
Last updated: October 28, 2022
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2012

Actual date on which the first participant was enrolled.

This study is open to males and females > 18 years and < 81 years with a clinical diagnosis of blepharospasm.

Principal SponsorMerz Pharmaceuticals GmbH
Last updated: October 28, 2022
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

124 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 81 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Eye DiseasesEyelid DiseasesBlepharospasm

Criteria

3 inclusion criteria required to participate
Currently receiving incobotulinumtoxinA, abobotulinumtoxinA or onabotulinumtoxinA

Documented clinical diagnosis of blepharospasm

Male or female subject aged > 18 years and < 81 years

1 exclusion criteria prevent from participating
Previous treatment with rimabotulinumtoxinB in the last 2 treatment cycles

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 5 locations

Merz Investigative Site #0007

Fountain Valley, United StatesOpen Merz Investigative Site #0007 in Google Maps

Merz Investigative Site # 0002

Sarasota, United States

Merz Investigative Site # 0001

Boston, United States

Merz Investigative Site #003

Durham, United States
Completed5 Study Centers