Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00614263 · ClinicalTrials.gov registry record

A Study to Examine Levels of Sedation During Outpatient Colonoscopies

A clinical trial, sponsored by Baylor Research Institute.

Completed
Registry status
100
Enrollment target

NCT00614263: Completed study, sponsored by Baylor Research Institute.

NCT00614263 is a clinical trial that has completed, run by Baylor Research Institute. The registered enrollment target is 100 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00614263 has completed, sponsored by Baylor Research Institute.

COMPLETED
Registry status
100 participants
Enrollment target

Study Summary

Examine levels of sedation required for patients to comfortably undergo colonoscopy using propofol and if adjunct monitoring equipment promotes patient safety.

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2006-03
Est. Completion 2006-12
Baylor Research Institute

180 total trials

What the finished NCT00614263 record still lists

NCT00614263 is an observational study that tracks outcomes without assigning an intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT00614263 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00614263 about?

NCT00614263 is a clinical study titled "A Study to Examine Levels of Sedation During Outpatient Colonoscopies". Examine levels of sedation required for patients to comfortably undergo colonoscopy using propofol and if adjunct monitoring equipment promotes patient safety.

What is the current status of trial NCT00614263?

This trial is currently completed. The enrollment target is 100 participants. The study started on 2006-03. Estimated completion is 2006-12.

Who is sponsoring clinical trial NCT00614263?

This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00614263, the US trial registry maintained by the National Library of Medicine. NCT00614263 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.