Confocal Laser Endomicroscopy
Primary Purpose
Digestive System Diseases
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Colonoscopy
Endoscopy
Sponsored by
About this trial
This is an interventional diagnostic trial for Digestive System Diseases focused on measuring Confocal laser endomicroscopy, cancerous and non-cancerous conditions, tolerance, intravenous fluorescein, Digestive symptoms or disease requiring an endoscopy procedure (upper GI endoscopy or colonoscopy) performed under general anaesthesia
Eligibility Criteria
Inclusion criteria:
- Patient between 18 to 70 years-old
- Symptoms or disease requiring an upper GI endoscopy or a colonoscopy performed under general anaesthesia
- Written informed consent obtained
Exclusion criteria:
- No indication for upper GI endoscopy or colonoscopy
- Treatment by beta-blockers
- Coagulopathy
- Dialysis for impaired renal function
- Pregnancy or breast-feeding
- Known allergy to fluorescein
- Pace-maker
- Severe cardiac or liver disease
- Emergency context- Zenker's diverticulum (for upper GI endoscopy) or recently complicated colonic diverticulosis (for colonoscopy)
- Patient's refusal
Sites / Locations
- Service d'Hépato-Gastroentérologie, Centre Hospitalier Lyon Sud
- Service d'Hépato-Gastroentérologie, Institut Paoli Calmettes
- Service d'Hépato-Gastroentérologie, CHU Nantes
- Service d' hépato-gastro-entérologie, CHU de ROUEN
- CHU de Rangueil
Outcomes
Primary Outcome Measures
To establish a safe and standardized practice of CLE in France, which should give a possibility, by providing high quality optical biopsies, to perform in vivo diagnosis of different digestive diseases
Secondary Outcome Measures
To assess the tolerance of CLE in terms of frequency and gravity of potential adverse events related to the injection of fluorescein
To assess the diagnostic yield of CLE in various clinical conditions (cancerous and non-cancerous diseases) by comparing optical biopsies with standard histology
To assess the interobserver agreement for this technique, using a database of optical biopsies created at the end of the study
Full Information
NCT ID
NCT00561938
First Posted
November 20, 2007
Last Updated
February 24, 2009
Sponsor
Nantes University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00561938
Brief Title
Confocal Laser Endomicroscopy
Official Title
Confocal Laser Endomicroscopy in the Digestive Tract: A Multicentre French Pilot Study.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Nantes University Hospital
4. Oversight
5. Study Description
Brief Summary
Confocal laser endomicroscopy (CLE) is a new diagnostic technique that allows microscopic examination of the digestive mucosa during ongoing endoscopy. Different types of tissue and diseases can be diagnosed immediately, and analysis of the in vivo microarchitecture is helpful to better target standard biopsies and reduce the number of biopsies required. CLE necessitates an intravenous injection of a fluorescent marker, e.g. fluorescein, to obtain 'optical biopsies' with a high level of magnification (up to 1000 fold). To date, more than 1000 endomicroscopy procedures have been performed in the world and different publications have shown the safety, feasibility and excellent diagnostic yield of CLE. No complication related to IV injection of fluorescein has been reported. However, all these data come from a very limited number of expert centres and need to be confirmed and validated at the multicenter level. The aims of this multicenter trial are: 1) to standardize CLE in all centres equipped in France, 2) to ensure the safety of intravenous fluorescein injection, 3) to test the diagnostic value of CLE in various conditions representative of the large spectrum of different cancerous and non-cancerous digestive diseases.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Digestive System Diseases
Keywords
Confocal laser endomicroscopy, cancerous and non-cancerous conditions, tolerance, intravenous fluorescein, Digestive symptoms or disease requiring an endoscopy procedure (upper GI endoscopy or colonoscopy) performed under general anaesthesia
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
61 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Colonoscopy
Intervention Description
microscope with a confocal window in its distal part. During ongoing endoscopy, 5 mL of 10% fluorescein (Novartis) will be injected intravenously to perform CLE imaging. In brief, CLE images are obtained few seconds after fluorescein injection by gentle positioning of the confocal window in contact with the digestive mucosa. To stabilize images, some suction can be applied using the operating channel of the endoscope. CLE images ('optical biopsies') will be stored and 1-2 standard biopsies will be performed in the examined area in order to further compare optical and standard biopsies. The overall duration of the procedure will be limited to 1 hour. During and after the procedure, patients will be monitored and surveyed continuously by anaesthesiologist. General tolerance and potential late adverse events will be assessed by the careful inquiry performed 1 month after the procedure by consultant gastroenterologist.
Intervention Type
Procedure
Intervention Name(s)
Endoscopy
Intervention Description
After obtaining a written informed consent from all the patients, standard upper GI endoscopy or colonoscopy will be performed under general anaesthesia using a videoendoscope EC-3870 (Pentax), which includes a miniaturized microscope with a confocal window in its distal part. During ongoing endoscopy, 5 mL of 10% fluorescein (Novartis) will be injected intravenously to perform CLE imaging. In brief, CLE images are obtained few seconds after fluorescein injection by gentle positioning of the confocal window in contact with the digestive mucosa. To stabilize images, some suction can be applied using the operating channel of the endoscope. CLE images ('optical biopsies') will be stored and 1-2 standard biopsies will be performed in the examined area in order to further compare optical and standard biopsies. The overall duration of the procedure will be limited to 1 hour. During and after the procedure, patients will be monitored and surveyed continuously by anaesthesiologist.
Primary Outcome Measure Information:
Title
To establish a safe and standardized practice of CLE in France, which should give a possibility, by providing high quality optical biopsies, to perform in vivo diagnosis of different digestive diseases
Secondary Outcome Measure Information:
Title
To assess the tolerance of CLE in terms of frequency and gravity of potential adverse events related to the injection of fluorescein
Title
To assess the diagnostic yield of CLE in various clinical conditions (cancerous and non-cancerous diseases) by comparing optical biopsies with standard histology
Title
To assess the interobserver agreement for this technique, using a database of optical biopsies created at the end of the study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Patient between 18 to 70 years-old
Symptoms or disease requiring an upper GI endoscopy or a colonoscopy performed under general anaesthesia
Written informed consent obtained
Exclusion criteria:
No indication for upper GI endoscopy or colonoscopy
Treatment by beta-blockers
Coagulopathy
Dialysis for impaired renal function
Pregnancy or breast-feeding
Known allergy to fluorescein
Pace-maker
Severe cardiac or liver disease
Emergency context- Zenker's diverticulum (for upper GI endoscopy) or recently complicated colonic diverticulosis (for colonoscopy)
Patient's refusal
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Paul Galmiche, PhD
Organizational Affiliation
Nantes University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service d'Hépato-Gastroentérologie, Centre Hospitalier Lyon Sud
City
Lyon
ZIP/Postal Code
69495
Country
France
Facility Name
Service d'Hépato-Gastroentérologie, Institut Paoli Calmettes
City
Marseille
ZIP/Postal Code
13009
Country
France
Facility Name
Service d'Hépato-Gastroentérologie, CHU Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Service d' hépato-gastro-entérologie, CHU de ROUEN
City
Rouen
ZIP/Postal Code
76031
Country
France
Facility Name
CHU de Rangueil
City
Toulouse
ZIP/Postal Code
31059
Country
France
12. IPD Sharing Statement
Learn more about this trial
Confocal Laser Endomicroscopy
We'll reach out to this number within 24 hrs