Evaluation of Postoperative Blood Pressure Changes After Benign Gynecologic Surgery

This study is currently recruiting participants.

Verified by University of Rochester, September 2008

First Received: September 19, 2008 Last Updated: September 22, 2008 History of Changes

Sponsored by:	University of Rochester
Information provided by:	University of Rochester
ClinicalTrials.gov Identifier:	NCT00757484

Purpose

The purpose of this study is to establish normal postoperative changes in blood pressure in women undergoing scheduled gynecologic surgery requiring inpatient postoperative care. Also, to establish if there is a difference in normal postoperative blood pressure changes between elderly and non-elderly women undergoing scheduled gynecologic surgery requiring inpatient postoperative care.

Condition
Urogynecology

MedlinePlus related topics: Surgery

U.S. FDA Resources

Study Type:	Observational
Study Design:	Cohort, Retrospective
Official Title:	Evaluation of Postoperative Blood Pressure Changes After Benign Gynecologic Surgery

Further study details as provided by University of Rochester:

Primary Outcome Measures:

Women who underwent scheduled gynecologic surgery requiring inpatient postoperative care [ Time Frame: January 2007 to January 2008 ] [ Designated as safety issue: No ]

Estimated Enrollment:	250
Study Start Date:	September 2008

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	Yes
Sampling Method:	Non-Probability Sample

Study Population

Gynecologic patients

Criteria

Inclusion Criteria:

Women who underwent scheduled gynecologic surgery requiring inpatient postoperative care between January 2007 - January 2008

Exclusion Criteria:

Women who experienced myocardial infarction, cardiac arrest or failure, pulmonary embolism, infection requiring intravenous antibiotics, intra- or postoperative hemorrhage requiring blood transfusion, renal failure

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00757484

Contacts

Contact: Erin Duecy, MD

585-273-3232

Locations

United States, New York
University of Rochester	Recruiting
Rochester, New York, United States, 14642
Contact: Erin Duecy, MD 585-273-3232

Sponsors and Collaborators

University of Rochester

Investigators

Principal Investigator:

Erin Duecy, MD

University of Rochester

More Information

No publications provided

Responsible Party:	University of Rochester ( Erin Duecy, MD )
Study ID Numbers:	25003
Study First Received:	September 19, 2008
Last Updated:	September 22, 2008
ClinicalTrials.gov Identifier:	NCT00757484 History of Changes
Health Authority:	United States: Institutional Review Board

ClinicalTrials.gov processed this record on May 07, 2009