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NCT03610425 Clinical Trial

A Standardized Bundle Protocol to Optimize Outcomes With Patients Undergoing Gynecological Surgery

Hysterectomy Clinical Trial

Official title:
A Standardized Bundle Protocol to Optimize Outcomes With Patients Undergoing Gynecological Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03610425
Other study ID # 1088437
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 17, 2017
Est. completion date February 28, 2018

Study information
Verified date July 2018
Source HonorHealth Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Difference in outcome measures with the addition of post-operative evidence based bundle pre-operative education compared to standard pre-operative education given to patients prior to hysterectomy.

Description:

The purpose of this project is to evaluate whether there is a difference in outcome measures (length of stay, occurrence of readmission, and patient satisfaction) with the addition of a post-operative evidence-based bundle/standard pre-operative education compared to standard pre-operative education alone that is given to patients prior to a hysterectomy (open, vaginal, or laparoscopic).

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date February 28, 2018
Est. primary completion date January 19, 2018
Accepts healthy volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who are admitted for all hysterectomies from October 1, 2017 through December 31, 2017, who speak English, and who are discharged home.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States HonorHealth Scottsdale Thompson Peak Scottsdale Arizona

Sponsors (1)
Lead Sponsor Collaborator
HonorHealth Research Institute

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Length of Stay Number of days spent in the hospital from the first post-operative day to the day of discharge 0 to 30 days
Primary Occurrence of Re-Admission Re-admission within 30 days will be measured through the EMR 0 to 30 days
Primary Patient Satisfaction Patient Satisfaction Survey that consists of 7 questions utilizing a likert scale from excellent to poor 0 to 30 days
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