- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00435383
Comparing Oxygen Saturation in Post Anesthesia Care Unit After Different Methods of Pain Relief
December 11, 2015 updated by: Samia Khalil, The University of Texas Health Science Center, Houston
Oxygen Saturation During Transfer From Operating Room to Post Anesthesia Care Unit After Current Anesthesia Care
To determine the which method of pain relief is better after current anesthesia care.
Study Overview
Status
Completed
Conditions
Detailed Description
We hypothesized that in children, the current anesthesia care (combined light general anesthesia and caudal analgesia) may decrease incidence of intra and or postoperative de-saturation( SaO2 < %95), the need of oxygen during child's transport to the PACU and during his stay in the recovery room, compared with children who receive intravenous narcotics for intra and postoperative pain relief.
Study Type
Observational
Enrollment (Anticipated)
42
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Texas
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Houston, Texas, United States, 77030
- University of Texas,Anesthesiology Department
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 6 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Sampling Method
Probability Sample
Study Population
Children scheduled for elective uni or bilateral orchidopexy.
Description
Inclusion Criteria:
- Healthy children
- ASA physical status 1 or 2
- 1-6 yr old
- Scheduled for elective uni or bilateral orchidopexy
Exclusion Criteria:
- Children with compromised pulmonary, cardiac, neurological, hematological, renal condition, with history of prematurely or are obese will be excluded.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Observational
Group 1 received a presurgical caudal block and group 2 received a intravenous narcotics.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Samia Khalil, M.D., University of Texas, Houston, Texas
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2003
Primary Completion (Actual)
February 1, 2007
Study Completion (Actual)
October 1, 2008
Study Registration Dates
First Submitted
February 13, 2007
First Submitted That Met QC Criteria
February 14, 2007
First Posted (Estimate)
February 15, 2007
Study Record Updates
Last Update Posted (Estimate)
December 14, 2015
Last Update Submitted That Met QC Criteria
December 11, 2015
Last Verified
December 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HSC-MS-02-220
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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