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Completed

NCT Number: NCT04870242

Studding the Implementation of ERAS Protocols in Pediatric Surgery

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

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Key information

Conditions

ERAS Appendicitis Cecal Diseases Digestive System Diseases Endocrine System Diseases Gastroenteritis Gastrointestinal Diseases Genital Diseases Genital Diseases, Male Gonadal Disorders Hydrocele Infections Intestinal Diseases Intraabdominal Infections Male Urogenital Diseases Pediatric Disorder Testicular Diseases Testicular Hydrocele Urogenital Diseases

Age range

6 month–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Of Jordan

Amman, Amman, Jordan, 11941, Jordan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Observational study, non-interventional

Other

observational study for the ERAS protocols in pediatric surgery

Primary outcomes

  1. Duration of Hospital stay,

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

  2. Total Hospital expenses

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

  3. readmission within 30 days

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

  4. reoperation within 90 days

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

  5. post op ER visits

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

  6. Pain control, according to a scale from 0-10, post-operative pain after implementation of ERAS protocols

    Time frame: retrospectively studied. data collection done at least 1 year after surgery

Sponsors and collaborators

Lead sponsor

University of Jordan

Other

Registry information

Official study title

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

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
May 3, 2021
Registry last updated
May 3, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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