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NCT06152601: LevPOS

Early Standing in Minors Operated on for Idiopathic Scoliosis

Status unknown NA Last updated 21 March 2024
What this trial tests

NA trial testing anticipated bipedal standing position in the immediate post-operative phase in Idiopathic Scoliosis in 30 participants. Status unknown.

Timeline
19 March 2024
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorUniversity Hospital, Toulouse
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment30
Start date19 March 2024
Primary completion31 December 2025
Estimated completion31 December 2025
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Toulouse

Who can join

Adults 12 to 18, any sex, with Idiopathic Scoliosis or ERAS. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Idiopathic Scoliosis

Currently open trials in the same condition.

Other University Hospital, Toulouse trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06152601.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing