N/A
N=491
Evaluation of Postoperative Blood Pressure Changes After Benign Gynecologic Surgery
Urogynecology
Bottom Line
View on ClinicalTrials.gov: NCT00757484 ↗Enrolled (actual)
491
Serious AEs
—
Results posted
Dec 2015
Primary outcome: Primary: Percentage of Participants Who Underwent Gynecologic Surgery — 42; 32; 26 percentage of participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- University of Rochester
- Primary completion
- Sep 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Participants Who Underwent Gynecologic Surgery |
42; 32; 26 | — |
| SECONDARY Percentage of Women With Asymptomatic Hypotension |
22.8; 17.7 | — |
| SECONDARY Percentage of Participants Undergoing Different Types of Anesthesia |
92; 4; 6 | — |
| SECONDARY Surgical Time |
146 | — |
Summary
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.
Eligibility 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
Data sourced from ClinicalTrials.gov (NCT00757484). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.