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Interdisciplinary Scoliosis Correction Program.

Strategies for the Implementation of an Interdisciplinary Juvenile Scoliosis Correction Program Based on ERAS Principles. Before-after Study.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05159505
Enrollment
120
Registered
2021-12-16
Start date
2021-12-01
Completion date
2022-09-30
Last updated
2021-12-16

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

Conditions

Complication of Surgical Procedure, Complication,Postoperative, ERAS, Scoliosis, Scoliosis Idiopathic, Scoliosis; Juvenile

Brief summary

The aim of this study is to compare the outcomes after scoliosis surgery before and after the implementation of an interdisciplinary juvenile scoliosis correction program in teenager based on ERAS (enhanced recovery after surgery) principles.

Detailed description

Creating an optimal protocol for interdisciplinary care in the perioperative period in terms of therapeutic management (anesthesia and surgery schedule), as well as care, rehabilitation and ensuring mental well-being determines the real impact on the reduction of the risk of complications in the perioperative period. Enhanced recovery after surgery (ERAS) protocol has been found to result in reduced lenght of stay and complications in adult patients. Data in pediatric population remains modest. In addition to ERAS principles our terapeutic team has created a special educational application for better patient preparation for surgery. The purpose of the application is to explain the general rules of conduct in the process of preparing and carrying out surgery, anesthesia, prehabilitation and physiotherapy in children undergoing orthopedics surgery (e.g. spine surgery for adolescent idiopathic scoliosis). Hypothesis: Implementing an interdisciplinary juvenile scoliosis correction program based on ERAS principles and special educational app. will improve patient outcomes leading to a statistically significant reduction in post-operative pain and opioids demand, complication rate, length of stay without increasing readmissions and cost.

Interventions

None listed

Sponsors

Pomeranian Medical University Szczecin
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* patient with age \< 18 years * patient scheduled for idiopatic scoliosis surgery

Exclusion criteria

* patient with age \> 18years others type of scoliosis

Design outcomes

Primary

MeasureTime frameDescription
type of complicationsup to 4 weeks after surgerysurgery and anaesthesia complications

Secondary

MeasureTime frameDescription
Postoperative length of hospital stayup to 4 weeks after surgeryPostoperative length of hospital stay
Number of Analgetics consumptionup to 6 days after surgeryconsumption including opioids and non-opioids drug
Time to first bowel motionup to 6 days after surgeryAble to eat without abdominal discomfort, nausea, or vomiting
Time to first verticalizationup to 6 days after surgery

Countries

Poland

Contacts

Primary ContactJowita Biernawska, MD PhD
lisienko@wp.pl501337073

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026