Post-Operative Pain Management in Patients Undergoing Uterine Artery Embolisation for Symptomatic Leiomyomata

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ClinicalTrials.gov Identifier: NCT00163930

Recruitment Status : Unknown

Verified September 2005 by Bayside Health.
Recruitment status was: Recruiting

First Posted : September 14, 2005

Last Update Posted : October 3, 2006

Sponsor:

Information provided by:

Bayside Health

No Study Results Posted on ClinicalTrials.gov for this Study

About Study Results Reporting on ClinicalTrials.gov

Recruitment Status :	Unknown
Primary Completion Date :	No date given
Study Completion Date :	December 2007

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Konstantatos AH, Kavnoudias H, Stegeman JR, Boyd D, Street M, Bailey M, Lyon SM, Thomson KR. A randomized, double-blind, placebo-controlled study of preemptive oral oxycodone with morphine patient-controlled anesthesia for postoperative pain management in patients undergoing uterine artery embolization for symptomatic uterine fibroids. Cardiovasc Intervent Radiol. 2014 Oct;37(5):1191-7. doi: 10.1007/s00270-014-0913-2. Epub 2014 Jul 1.

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