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Clinical Trials/NCT04008654
NCT04008654
Completed
Not Applicable

Implementation of ERAS Protocol in Patients Undergoing Surgery for Urinary Incontinence or Pelvic Organ Prolapse

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country120 target enrollmentJuly 5, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Urinary Incontinence
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Enrollment
120
Locations
1
Primary Endpoint
Hospital stay
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

ERAS protocols have been shown to improve recovery in terms of reduced pain, shortened time to ambulation and length of hospital stay. This study aims to investigate the impact of ERAS protocol on time to mobilization and length of hospital stay in patients undergoing surgery for urinary incontinence and pelvic prolapse.

Detailed Description

ERAS protocols containing several preoperative, intraoperative and postoperative measures have been shown to improve recovery in terms of reduced pain, shortened time to ambulation and length of hospital stay in patients undergoing surgery. However, data concerning the role of ERAS protocols in urogynecological surgery is limited. The present study, therefore, aimed to address the role of ERAS protocols in patients undergoing surgery for urinary incontinence and pelvic prolapse.

Registry
clinicaltrials.gov
Start Date
July 5, 2019
End Date
February 20, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Huseyin Kiyak

Principal Investigator, M.D.

Kanuni Sultan Suleyman Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Must be scheduled for surgery because of urinary incontinence or pelvic organ prolapse

Exclusion Criteria

  • Insulin dependent diabetes

Outcomes

Primary Outcomes

Hospital stay

Time Frame: Up to 1month

Length of hospital stay

Ambulation

Time Frame: Up to 1 week

Time to ambulation

Study Sites (1)

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