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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04249180
Other study ID # RECHMPL20_0036
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 1, 2019
Est. completion date July 1, 2020

Study information

Verified date July 2020
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluate the illness experience of patients with keratoconus as well as the rubbing habits of this population compared to the general population. To do this, the investigators used a questionnaire made by a Bordeaux team with questions on the experience of the patients' illness, their management and their friction habits


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 1, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria:

- Having a keratonus at least in one eyes

Exclusion criteria:

- Refus to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France UH Montpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess whether eye rubbing is a risk factor for keratoconus Assess whether eye rubbing is a risk factor for keratoconus 1 day
Secondary Evaluate the habits of the population with a keratoconus Evaluate the habits of the population with a keratoconus by a questionnaire completed by the patient 1 day
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