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Interdisciplinary Scoliosis Correction Program.

P

Pomeranian Medical University Szczecin

Status

Unknown

Conditions

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

Study type

Observational

Funder types

Other

Identifiers

NCT05159505
KB-0012/126/10/2021/Z

Details and patient eligibility

About

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.

Full 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.

Enrollment

120 estimated patients

Sex

All

Ages

10 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patient with age < 18 years
  • patient scheduled for idiopatic scoliosis surgery

Exclusion criteria

  • patient with age > 18years others type of scoliosis

Trial design

120 participants in 3 patient groups

"the before" group
Description:
40 teenagers after scoliosis surgery before interdisciplinary program implementation
"the after" group 1
Description:
40 teenagers after scoliosis surgery after ERAS program implementation
"the after" group 2
Description:
40 teenagers after scoliosis surgery after ERAS and educational program implementation

Trial contacts and locations

1

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Central trial contact

Jowita Biernawska, MD PhD

Data sourced from clinicaltrials.gov

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