Corneal ThicknessNCT01251705
Comparation of Different Devices to Measure Corneal Thickness
An observational study of Corneal Thickness, run by Technische Universität Dresden at 1 site in Germany.
Trial summary
Comparison of different methods for measuring peoples corneal thickness Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Corneal Thickness
- How many people
- 70 participants
- Where
- 1 siteGermany
- Study dates
- Nov 2010to Feb 2011
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: volunteers without corneal disease
Who may be able to join
- healthy cornea
Who cannot join
- myopia or astigmatism over 1,5 dpt
- corneal surgery
- acute ocular inflammation
- lost of vision
Trial locations and contacts
1 site in 1 country.
Germany1 site, 1 recruiting
- Recruiting
Departement of Ophthalmology
Dresden, Saxony, 01307
Haustein, Doctor med., 0049351458 ext. 3381, Michael.Haustein@uniklinikum-dresden.de
Wozniak, 0049351458 ext. 3381, Kathleen.Wozniak@uniklinikum-dresden.de
About this study
Comparison of different methods for measuring peoples corneal thickness
Read the detailed description
Volunteers with healthy corneas will be measured by different instruments to detect their corneal thickness. First interindividual difference between the instruments will be reviewed. People will be measured again two times on two different days to examine an interindividual difference in all instruments.
- Conditions
- Corneal Thickness
- Keywords
- Cornea, SL OCT, Spectral OCT Cornea modul, ultrasound pachymetry, Pentacam
- Medical subject headings
- Corneal Diseases
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Dec 2010 (estimated)
- Study startNov 2010
- Primary completionDec 2010 (estimated)
- Study completionFeb 2011 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Corneal ThicknessStudies of the same condition, open and under way.
- More trials run by Technische Universität DresdenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 70 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Technische Universität Dresden
- Sponsor type
- University, hospital or other
- Investigators
- Haustein, Doctor med., Principal investigator, Departement of Ophthalmology University of Dresden
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01251705
- Sponsor's protocol ID
- CompCornea
- Status last verified
- Dec 2010
- First submitted
- 1 Dec 2010
- Last updated
- 2 Dec 2010
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Dec 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparation of Different Devices to Measure Corneal Thickness
- ClinicalTrials.gov ID
- NCT01251705
- Acronym / sponsor ID
- CompCornea
- Conditions
- Corneal Thickness
- Keywords
- Cornea, SL OCT, Spectral OCT Cornea modul, ultrasound pachymetry, Pentacam
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 70 participants (estimated)
- Lead sponsor
- Technische Universität DresdenUniversity, hospital or other
- Study start
- Nov 2010
- Primary completion
- Dec 2010 (estimated)
- Study completion
- Feb 2011 (estimated)
- First posted
- 2 Dec 2010 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Comparison of different methods for measuring peoples corneal thickness
Detailed description
Volunteers with healthy corneas will be measured by different instruments to detect their corneal thickness. First interindividual difference between the instruments will be reviewed. People will be measured again two times on two different days to examine an interindividual difference in all instruments.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- volunteers without corneal disease
Key inclusion criteria (1 listed)
- healthy cornea
Key exclusion criteria (4 listed)
- myopia or astigmatism over 1,5 dpt
- corneal surgery
- acute ocular inflammation
- lost of vision
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Dec 2010.
Related trials for Corneal Thickness
Not yet recruitingObservational study
Thick Cornea with High Back Elevation
Corneal Thickness Measurement
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Haustein, Doctor med. principal investigator
Departement of Ophthalmology University of Dresden
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Corneal Thickness, run by Technische Universität Dresden at 1 site in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 2 Dec 2010. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Haustein, Doctor med. (0049351458 ext. 3381, Michael.Haustein@uniklinikum-dresden.de), or a site near the patient. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Dec 2010; AzTrials last refreshed its copy on 7 Nov 2026.