Early Standing in Children and Adolescent Operated on for Idiopathic Scoliosis

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The implementation of an enhanced rehabilitation after surgery (ERAS) program in major orthopedic surgery and in scoliosis surgery in children and adolescents has become a marker of good practice. Investigators are already applying anesthetic, surgical, peri-operative medicine and rehabilitation techniques allowing accelerated and improved rehabilitation for scoliosis operated patients in the establishment. To improve patient care, the Investigators want to develop the ERAS program. The objective of this research will be to validate the feasibility of getting up early on D0 in post-anesthesia care unit (PACU) or ICU in children who have just had surgery for idiopathic scoliosis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 18
Healthy Volunteers: f
View:

• Programming of spinal surgery via the posterior approach for idiopathic scoliosis eligible for an ERAS program

• Person affiliated or beneficiary of a social security scheme

• Free, informed and written consent signed by the legal guardians of the minor patient

• Free and informed consent of the minor patient

Locations
Other Locations
France
CHU de TOULOUSE
RECRUITING
Toulouse
Contact Information
Primary
François Dr DELORT
delort.f@chu-toulouse.fr
05 34 55 85 33
Backup
Delphine Dr KERN
kern.d@chu-toulouse.fr
Time Frame
Start Date: 2024-03-19
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 30
Treatments
Experimental: Group experimental
Patient between 12 and 18 years old with a spinal surgery for idiopathic scoliosis programmed. Immediately postoperatively, during his stay in a PACU or ICU, the patient will be offered a physiotherapy session including a lifting phase in a bipedal standing position.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Toulouse

This content was sourced from clinicaltrials.gov