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NCT04870242 Clinical Trial

Studding the Implementation of ERAS Protocols in Pediatric Surgery

Appendicitis Clinical Trial

Official title:
Enhanced Recovery After Surgery in Pediatric Surgery in Jordan: A Retrospective Cohort Study in a Tertiary University Hospital

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04870242
Other study ID # 67/2019/6216
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date March 1, 2021

Study information
Verified date April 2021
Source University of Jordan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

this is a retrospective cohort, descriptive study, investigating the role of ERAS protocols, in pediatric surgery and evaluate the feasibility and effectiveness of implementing these protocols

Recruitment information / eligibility
Status Completed
Enrollment 178
Est. completion date March 1, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 6 Months to 18 Years
Eligibility Inclusion Criteria: - all patients aged 6months -18 years, who underwent pediatric surgeries at a single tertiary institution Exclusion Criteria: - patients who had co-morbidities that might affect the outcome of the enhanced recovery and those who were younger than 6 months.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Observational study, non-interventional
observational study for the ERAS protocols in pediatric surgery

Locations
Country Name City State
Jordan University Of Jordan Amman Amman, Jordan

Sponsors (1)
Lead Sponsor Collaborator
University of Jordan

Country where clinical trial is conducted

Jordan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Duration of Hospital stay, retrospectively studied. data collection done at least 1 year after surgery
Primary Total Hospital expenses retrospectively studied. data collection done at least 1 year after surgery
Primary readmission within 30 days retrospectively studied. data collection done at least 1 year after surgery
Primary reoperation within 90 days retrospectively studied. data collection done at least 1 year after surgery
Primary post op ER visits retrospectively studied. data collection done at least 1 year after surgery
Primary Pain control, according to a scale from 0-10, post-operative pain after implementation of ERAS protocols retrospectively studied. data collection done at least 1 year after surgery
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