Confocal Laser Endomicroscopy in Patients With Eosinophilic Esophagitis
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ClinicalTrials.gov Identifier: NCT01234376 |
Recruitment Status :
Completed
First Posted : November 4, 2010
Last Update Posted : December 14, 2020
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Confocal laser endomicroscopy enables in vivo microscopic imaging within the mucosa layer of the gut at a subcellular resolution. Various studies have addressed the potential of endomicroscopy for the in vivo diagnosis of esophageal squamous cell carcinoma, Barrett´s esophagus and esophageal adenocarcinoma. Currently, there is only one case report from our group who noted the utility of endomicroscopy for the in vivo diagnosis of eosinophilic esophagitis.
The purpose of this study is to determine whether endomicroscopy is effective for the in vivo diagnosis of eosinophilic esophagitis.
Condition or disease | Intervention/treatment |
---|---|
Eosinophilic Esophagitis | Device: Confocal laser endomicroscopy |
Study Type : | Observational |
Actual Enrollment : | 45 participants |
Observational Model: | Other |
Time Perspective: | Prospective |
Official Title: | Confocal Laser Endomicroscopy in Patients With Eosinophilic Esophagitis |
Actual Study Start Date : | November 2010 |
Actual Primary Completion Date : | November 2014 |
Actual Study Completion Date : | December 2014 |

Group/Cohort | Intervention/treatment |
---|---|
Control patients |
Device: Confocal laser endomicroscopy
Confocal laser endomicroscopy |
Patients with eosinophilic esophagitis |
Device: Confocal laser endomicroscopy
Confocal laser endomicroscopy |
- Effectiveness of endomicroscopy for the in vivo diagnosis of eosinophilic esophagitis [ Time Frame: November 2010 - November 2012 ]
- Differentiation of mucosal alterations in patients with eosinophilic esophagitis compared to patients with gastroesophageal reflux disease. [ Time Frame: November 2010 - November 2012 ]

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Ages Eligible for Study: | 18 Years to 85 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Probability Sample |
Patients with eosinophilic esophagitis who underwent EGD for the evaluation of their symptoms.
Control patients who underwent EGD because of other reasons.
Inclusion Criteria:
- Written informed consent
- Age 18-85 years
- Ability of subjects to understand character and individual consequences of clinical trial
- Subjects undergoing EGD
Exclusion Criteria:
- Inability to provide written informed consent
- Severe Coagulopathy (Prothrombin time < 50% of control, Partial thromboplastin time > 50 s)
- Impaired renal function (Creatinine > 1.2 mg/dl)
- Pregnancy or breast feeding
- Active gastrointestinal bleeding
- Known allergy to fluorescein, acriflavin or cresyl violet
- Residing in institutions (e.g. prison)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01234376
Germany | |
University of Erlangen-Nuremberg | |
Erlangen, Bayern, Germany, 91054 |
Study Director: | Markus F. Neurath, M.D., Ph.D. | University of Erlangen-Nürnberg | |
Principal Investigator: | Helmut Neumann, M.D., Ph.D. | University of Erlangen-Nürnberg |
Responsible Party: | University of Erlangen-Nürnberg Medical School |
ClinicalTrials.gov Identifier: | NCT01234376 |
Other Study ID Numbers: |
HN-0003 |
First Posted: | November 4, 2010 Key Record Dates |
Last Update Posted: | December 14, 2020 |
Last Verified: | December 2020 |
Esophagitis Eosinophilic Esophagitis Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases Gastroenteritis |
Eosinophilia Leukocyte Disorders Hematologic Diseases Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |