Trials Sponsors Conditions Drugs Pricing

Conditions

General Anesthesia Laparoscopic Surgery Postoperative Surgery

Keywords

temperaturemonitorsurgery

Outcome Measures

Primary Outcomes (1)

To determine the accuracy of various temperature-monitoring methods and sites suitable for Post Anesthesia Care Unit use.
Discharge from Post Anesthesia Care Unit

Secondary Outcomes (1)

To quantify the core temperature changes that occur during transport from the Operating Room to the PostAnesthesia Care Unit.
PostAnesthesia Care Unit

Study Arms (1)

observation group

Patients undergoing laparoscopic surgery requiring general anesthesia and a bladder catheter.

Device: Body temperature thermometers

Interventions

Body temperature thermometersDevice

Temperature readings every 30 minutes during and post surgery using internal stethoscope, catheter and adhesive patches/electronic thermometer.

Also known as: 1. Distal esophagus (Mon-a-therm, Tyco-Mallinckrodt Anesthesia Products,, 2. Bladder (Mon-a-therm, Tyco-Mallinckrodt Anesthesia Products,, 3. Infrared-aural canal bilaterally (GENIUS Model 3000A, Kendall Healthcare), 4. Temporal artery with an electronic scanning thermometer (Model TAT-5000, Exergen), 5. Posterior sublingual pocket with electronic thermometer (Turbo Temperature Model 2180CX01EE), 6. Forehead skin thermocouple (Mon-a-therm, Tyco-Mallinckrodt Anesthesia Products), 7. Axilla with an electronic probe (Mon-a-therm, Tyco-Mallinckrodt Anesthesia Products), 8. Forehead liquid-crystal (Crystaline II), 9. Intermittent axillary temperature (Turbo Temperature Model 2180CX01EE), 10. "Deep" temperature with a 4-cm probe on the forehead, 11. "Deep" temperature with a 7-cm probe over the subclavicular region of the upper chest

observation group

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years - 80 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Patients undergoing laparoscopic surgery requiring general anesthesia and a bladder catheter.

You may qualify if:

to 80 years of age

Sponsors & Collaborators

The Cleveland Clinic
Otherlead

Study Sites (1)

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Study Officials

Daniel I Sessler, MD
The Cleveland Clinic
STUDY CHAIR
Daniel I Sessler, MD
The Cleveland Clinic
PRINCIPAL INVESTIGATOR

Enrollment

50 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

January 31, 2008

First Posted

February 13, 2008

Study Start

January 2008

Date type not reported

This date has not been verified as actual or estimated.

Temperature Measurement in Post-Anesthesia Care Units

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

observation group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

observation group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations