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OpenTrials
Completed

NCT Number: NCT00435383

Comparing Oxygen Saturation in Post Anesthesia Care Unit After Different Methods of Pain Relief

To determine the which method of pain relief is better after current anesthesia care.

Completed

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Key information

Age range

1 year–6 year

Sex eligibility

Male

Study type

Observational

Primary location

University of Texas,Anesthesiology Department

Houston, Texas, 77030, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Official study title

Oxygen Saturation During Transfer From Operating Room to Post Anesthesia Care Unit After Current Anesthesia Care

Important dates

Study start
2003
Primary completion
2007
Study completion
2008
First posted
Feb 15, 2007
Registry last updated
Dec 14, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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