Multicentric Evaluation of Enhanced Recovery After Surgery Protocol in Adolescent Idiopathic Scoliosis Surgery
- Idiopathic Scoliosis
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Hospices Civils de Lyon
- Enrolment target
- 316
- Started
- 21 September 2026
- Main results due
- 21 August 2030
- Study sites
- 11
- Registry updated
- 24 September 2026
Can you take part?
- Ages 11 years to 17 years.
- Open to any sex.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: * Adolescents between 11 and 17 years old * Adolescent idiopathic scoliosis diagnosis * Posterior vertebral fusion surgery indicated to treat the patient * Informed consent signed by both parents / legal guardians Exclusion Criteria: * Comorbidities that might influence the duration of hospitalization (e.g. respiratory failure, diabetes…) * Previous spine surgery * Patient not benefiting from an health insurance plan * Pregnant, parturient or breastfeeding woman * Patient benefiting of psychiatric care * Patient subject to a legal protection measure (guardianship, curatorship)
What this study is about
In the sponsor’s own words, from the registry.
Adolescent idiopathic scoliosis is a deformation of the spine affecting 2 to 4% of under 18 years old population. This can have severe physical or psychological impact during adulthood. The deformation causes mechanical constraints resulting in early osteoarthritis, which results in adulthood disability.
There is also an impact on the respiratory function in most severe cases of idiopathic scoliosis. Adolescents affected by a scoliosis with an angle of 40° of more undergo a surgery called posterior fusion during adolescence to limit these impacts.
In France, more than 1000 adolescent patients undergo a surgery called posterior spinal fusion for their severe scoliosis.
This aims to straighten the spine by bone grafting all the vertebras included in the scoliosis. Two metal rods are implanted to favour osteosynthesis of the straight spine.
This intervention suffer of a bad image and worries the patients and their parents, as it needs metal implants near the spinal cord.
The worry comes from the most severe complication that may happen exceptionally following this surgery, which is a definitive paraplegia. The scar is quite large and the surgery reduces the mobility of a part of the spine. The intervention produces a quite large haemorrhage, which leads to a diminution in haemoglobin level, resulting in a fatigue during the following weeks.
On the following days, the patient will need a specific protocol of pain management including morphine-based and anti-inflammatory drugs.
This intervention will often require a 5 to 7 days hospitalization with a 1 to 2 month convalescence period at home or in rehabilitation centre.
This intervention is performed on adolescent patients without comorbidities. Moreover, the surgical approach is not profound passing between the para-vertebral muscles with no close large blood vessels or major organs. The pain is caused by correction tensions and the access to the vertebras during the surgery.
Surgical techniques have considerably evolved allowing shorter interventions and to reduce the loss of blood.
The association between morphine-based treatments and grade I analgesics enables an effective pain management.
This intervention appears to perfectly suit to an enhanced recovery after surgery procedure (ERAS).
ERAS is a set of procedure meant to enhance its tolerance and to reduce its morbidity and the hospitalization duration after surgery and the recovery duration.
ERAS is well developed in adult patients undergoing surgery, it is also well described in paediatric patient especially on adolescent scoliosis surgeries.
As the pain is well controlled during the hospitalization as well when the patient get back home, there are very few obstacles to an ERAS procedure in this indication for a patient without comorbidities.
Numerous articles report experiences of medical staff with ERAS protocols.
Generally, the set of measures includes:
* Before surgery: Providing information and therapeutic patient education, iron supplementation, physiotherapy, skin disinfection, digestive preparation against constipation * During surgery: recuperations of blood cells to limit blood loss, use of modern tools to facilitate the positioning of pedicle screws, surgery performed by 2 surgeons * After surgery: Pain management until stopping of analgesics by patient and maintenance of a link between the patient at home and the hospital staff after end of hospitalization The articles published about ERAS reports a favourable experience of such protocols with an efficient pain management, reduced hospitalization durations without increasing morbidity or re-hospitalizations. However, no studies have studied and proved by a robust scientific method the benefits of ERAS in adolescent scoliosis.
No studies evaluate the patients' quality of life or follow the patient for more than 6 months after surgery (limiting the assessment of long term complications e.g. infectious complications).
The link between hospital staff and the patient after his return back home is not described as well.
This research project aims to confirm with a robust scientific approach that ERAS protocols in idiopathic scoliosis in adolescents allow to reduce the duration of hospitalization compared to standard of care procedures while improving quality of life after surgery.
Study sites(11)
CHU d'Amiens Site Sud
Amiens, France
Recruiting
CHU de Besançon Hopital Jean Minjoz
Besançon, France
Recruiting
Pediatric orthopedic surgery unit Hôpital femme Mère Enfant (HFME)
Bron, France
Recruiting
CHU de Grenoble Hôpital Couple Enfant
La Tronche, France
Recruiting
Centre Medico-Chirurgical de Réadaptation des Massues Croix-Rouge
Lyon, France
Recruiting
AP-HM Hôpital de la Timone
Marseille, France
Recruiting
Fondation LENVAL
Nice, France
Recruiting
CHU de Saint-Etienne Hôpital Nord
Saint-Priest-en-Jarez, France
Recruiting
CHU de Toulouse
Toulouse, France
Recruiting
Clinique Médipôle Garonne
Toulouse, France
Recruiting
Clinique St Leonard
Trélazé, France
Recruiting
Showing 11 of 11 sites. 11 of the 11 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT06908213. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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