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

NCT00695799 · ClinicalTrials.gov registry record

Propofol Concentration In The Ambient Air Of The Operating Room And In The Blood Of Anesthesia Care Providers

A clinical trial, sponsored by Rutgers, The State University of New Jersey.

Completed
Registry status
20
Enrollment target

NCT00695799: Completed study, sponsored by Rutgers, The State University of New Jersey.

NCT00695799 is a clinical trial that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00695799 has completed, sponsored by Rutgers, The State University of New Jersey.

COMPLETED
Registry status
20 participants
Enrollment target

Study Summary

The pollution of the operating room environment by anesthetic agents had been questioned, studied and documented in the past. These investigations demonstrated the existence of teratogenic effects in animals and the possibility of a decrease in mental performance, reduced fertility, fetal loss, spontaneous abortion and addictive potential in humans with chronic exposure to trace amounts of anesthetic agents. These findings led to the establishment of exposure limits and industry standards by consumer protection agencies, such as National Institute for Occupational Safety and Health (NIOSH). However, these standards applied to inhalation anesthetic agents that were excreted from the lungs of patients during expiration. These concerns about operating room pollution weaned away with the introduction of intravenous anesthetic agents, such as propofol, because it was believed propofol was excreted by systems other than the lungs. Recent research points to the contrary and demonstrates the excretion of propofol vapor in the expired gases of patients. Furthermore, animal experiments in our laboratory establish the existence of a biological mechanism responsible for addiction in animals exposed to trace amounts of propofol. We propose to study the exposure levels of anesthesia care providers in the operating room, during propofol use, under standardized conditions. Our findings will help to establish preventive measures for propofol addiction in anesthesia care providers.

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2008-06
Est. Completion 2010-12

What the finished NCT00695799 record still lists

NCT00695799 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.

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

NCT00695799 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00695799 about?

NCT00695799 is a clinical study titled "Propofol Concentration In The Ambient Air Of The Operating Room And In The Blood Of Anesthesia Care Providers". The pollution of the operating room environment by anesthetic agents had been questioned, studied and documented in the past. These investigations demonstrated the existence of teratogenic effects in animals and the possibility of a decrease in mental performance, reduced fertility, fetal loss, spon...

What is the current status of trial NCT00695799?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2008-06. Estimated completion is 2010-12.

Who is sponsoring clinical trial NCT00695799?

This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 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

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

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 NCT00695799, the US trial registry maintained by the National Library of Medicine. NCT00695799 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.