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

Cryptorchidism Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00435383
• Other study ID #: HSC-MS-02-220
• Status: Completed
• Phase: Phase 2
• First received: February 13, 2007
• Last updated: December 11, 2015
• Start date: March 2003
• Est. completion date: October 2008

Study information

• Verified date: December 2015
• Source: The University of Texas Health Science Center, Houston
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: October 2008
• Est. primary completion date: February 2007
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 1 Year to 6 Years

Eligibility

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 Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Cryptorchidism

Locations

Country	Name	City	State
United States	University of Texas,Anesthesiology Department	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States,