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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03610425

Enrollment

Registered

2018-08-01

Start date

2017-10-17

Completion date

2018-02-28

Last updated

2018-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hysterectomy

Brief 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.

Detailed 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).

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

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.

Design outcomes

Primary

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

Countries

United States

Outcome results