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NCT02101099 · ClinicalTrials.gov registry record
Effect of Anesthesia on Force Application During Colonoscopy
A clinical trial of Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases, sponsored by Artann Laboratories.
- Completed
- Registry status
- 102
- Enrollment target
- 3
- Study locations
NCT02101099: Completed study of Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases, sponsored by Artann Laboratories.
NCT02101099 is a study of Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases that has completed, run by Artann Laboratories. The registered enrollment target is 102 participants. The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02101099, a study of Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases, has completed, sponsored by Artann Laboratories.
- COMPLETED
- Registry status
- 102 participants
- Enrollment target
- 3
- Study locations
Study Summary
The aim of the study is to determine if more force is used during colonoscopy when patients receive monitored anesthesia with propofol versus conscious sedation. Force measurements will be performed using the colonoscopy force monitor (CFM). This device measures the magnitude and direction of force applied to the insertion tube of a standard colonoscope during colonoscopy.
Conditions Studied
Interventions
- DEVICE Colonoscopy Force Monitor
Study Locations (3)
District of Columbia
- Georgetown University Medical Center, Gastroenterology - Washington D.C.
Maryland
- Chevy Chase Endoscopy Center - Chevy Chase
Pennsylvania
- Univeristy of Pennsylvania Medical Center - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 102 participants |
| Start Date | 2014-03 |
| Est. Completion | 2015-12 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02101099
The ClinicalTrials.gov registry entry for NCT02101099 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 102 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Artann Laboratories, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases appearing as the primary indexed condition, and to 1 intervention - of which Colonoscopy Force Monitor is the first listed.
NCT02101099 reports 3 study locations spanning 3 distinct geographic areas - top geographies include District of Columbia, Maryland, Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT02101099 about?
NCT02101099 is a clinical study titled "Effect of Anesthesia on Force Application During Colonoscopy". The aim of the study is to determine if more force is used during colonoscopy when patients receive monitored anesthesia with propofol versus conscious sedation. Force measurements will be performed using the colonoscopy force monitor (CFM). This device measures the magnitude and direction of force ...
What is the current status of trial NCT02101099?
This trial is currently completed. The enrollment target is 102 participants. The study started on 2014-03. Estimated completion is 2015-12.
What conditions does trial NCT02101099 study?
This clinical trial studies the following conditions: Outpatient Colonoscopy for Colorectal Cancer Screening or for Symptoms Suggestive of Colonic Diseases.
What interventions are being tested in trial NCT02101099?
The interventions under investigation include: Colonoscopy Force Monitor (DEVICE).
Who is sponsoring clinical trial NCT02101099?
This trial is sponsored by Artann Laboratories, which has 14 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02101099 being conducted?
This trial has 3 study locations across District of Columbia, Maryland, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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