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
• Status: Completed
• 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
• 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
• 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.

Related Conditions & MeSH terms

• Hysterectomy

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