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COMPLETED

Effect of Anesthesia on Force Application During Colonoscopy

NCT02101099 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 102 participants
Start Date 2014-03
Est. Completion 2015-12

Sponsor

Artann Laboratories

6 total trials

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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. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02101099 reports 3 study locations spanning 3 distinct geographic areas — top geographies include District of Columbia, Maryland, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02101099?

The interventions under investigation include: Colonoscopy Force Monitor (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02101099?

This trial is sponsored by Artann Laboratories, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial