Scoliosis; Adolescence

15

Review clinical trials related to Scoliosis; Adolescence. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Tranexamic Acid in Pediatric Idiopathic Scoliosis Surgery

This study will evaluate whether tranexamic acid (TXA), a medication used to reduce bleeding, is effective and safe in children undergoing surgery for idiopathic scoliosis. Significant blood loss is common during this type of surgery and often requires blood transfusions. Participants will be randomly assigned to one of three groups: (1) TXA given as an intravenous bolus followed by continuous infusion, (2) TXA given as two intravenous bolus doses, or (3) placebo (saline). Neither the patients nor the medical team will know which treatment is given. The main goal is to compare how much blood is lost during and after surgery and whether TXA reduces the need for blood transfusions. The study will also assess safety, including the risk of side effects such as seizures or blood clots. Patients will be followed for up to 30 days after surgery.

Participants needed: 90
Trial details
Age: 10-18Biological sex: AllType: InterventionalSponsor: Poznan University of Medical SciencesUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Age 10 to 18 years [+3]

Congenital or acquired coagulopathy [+5]

Status: Not yet recruiting

Tegileridine for Postoperative Pain After Adolescent Scoliosis Surgery

The goal of this clinical trial is to see if a new pain medicine called Tegileridine is at least as effective as morphine (the standard treatment) for pain relief after spinal surgery in teenagers with scoliosis. This type of study is called a "non-inferiority" trial. The study will also carefully compare the safety of both medicines. The main questions it aims to answer are: Is Tegileridine no worse than morphine at controlling pain in the first 24 hours after surgery? How do the side effects (like sleepiness or nausea) of Tegileridine compare to those of morphine? Researchers will compare two different doses of Tegileridine against morphine. Neither the participants nor the doctors assessing them will know which medicine is being given. Participants in this study will: Receive one of the three pain medicine options through a pump (called a PCA pump) that they can control themselves after surgery. Use the pump for up to 48 hours. Regularly rate their pain levels using a simple number scale. Have their health closely monitored by the study team during this time.

Participants needed: 171
Trial details
Phase: Phase 4Age: 10-17Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Jun 17, 2026Locations: 6
Eligibility criteria

Aged 10 years to less than 18 years. [+3]

History of difficult airway, severe respiratory depression (SpO₂ < 90%), acute o... [+8]

Status: Recruiting

Studying Melatonin and Recovery in Teens

The goal of this feasibility clinical trial is to learn if melatonin can help teens having major musculoskeletal surgery by promoting healthy sleep. Melatonin is available as a dietary supplement that may be effective in promoting longer, higher quality sleep. This study will assess the feasibility and acceptability of melatonin for teens undergoing major musculoskeletal surgery, as well as determine optimal measured outcomes (sleep, pain, health-related quality of life) at short- and long-term follow-up.

Participants needed: 45
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Mar 18, 2026Locations: 1
Eligibility criteria

Age 12-18 years [+6]

Prescription medication for premorbid insomnia [+9]

Status: Recruiting

Yoga for Back Pain in Adolescent Scoliosis

The Problem: Adolescent Idiopathic Scoliosis (AIS), the pre-eminent spinal pathology affecting over 5% of children and adolescents, presents a pronounced spinal curvature exceeding 10 degrees, with prevalence amongst female adolescents at a ratio of 3:1 compared to males. A significant portion of these patients are not immediate candidates for surgical intervention. The acute shortage of viable non-operative management strategies, which is becoming increasingly imperative given the current barriers to physical therapy access and the growing opioid crisis. The investigator's research intends to explore the addition of a structured yoga protocol to standard of care. This research will thus explore the potential for improved relief and quality-of-life improvements for AIS patients not ready for surgery. Significance: AIS is a pervasive condition which correlates with chronic and episodic lower back pain, diminished sleep quality, and depressive symptoms. This extensive comorbid association coupled with the financial pressure to patients and the healthcare system cannot be understated. Needs Statement: There is a lack of sufficient non-operative management options for AIS. Many patients face limited access and require supplementary management strategies to address the patient's conditions effectively, creating a significant unmet need for non-pharmacological pain management interventions. This need is further highlighted in the context of the escalating opioid crisis, a leading cause of death among adolescents and young adults. Hypothesis: The introduction of a structured yoga protocol can serve as a non-inferior or even superior alternative to traditional standard of care i management of AIS, addressing both the physical and psychosocial aspects intertwined with the condition. IMPACT: Change in Problem Significance: This research trial aims to enhance current standard of care for patients grappling with AIS. If the trial demonstrates superiority of yoga, it will delineate a paradigm shift in the current care standards for AIS patients, fostering a move towards a more cost-effective and holistic approach. Yoga could help alleviate the burdens on the healthcare system by reducing costs and enhancing accessibility for patients. Improvement in Pediatric Orthopedics Practice: By paving the way for non-pharmacological interventions, the trial aspires to mitigate the reliance on opioids for pain management in the pediatric demographic, therefore promoting overall well-being. This project not only seeks to develop alternative pain management strategies amidst a growing opioid epidemic but also champions the cause of improving the quality of life for the pediatric population battling chronic conditions like AIS. It echoes the urgent call to innovate and expand upon the current strategies in place, steering the medical community towards a future where integrative approaches are not the exception but the norm. Ultimately, this research aspires to guide the trajectory of pediatric orthopedics towards a healthcare system that is more inclusive, accessible, and holistically oriented, thereby enhancing the quality of life for pediatric patients grappling with conditions like AIS. 2\. Objectives (include all primary and secondary objectives) Goals/Objectives: To create a randomized clinical trial aimed to evaluate the efficacy of yoga in conjunction with standard of care treatments for AIS patients. SPECIFIC AIMS Aim 1: Evaluate the feasibility and challenges of implementing a yoga protocol for AIS patients. Methodology: Online class attendance, survey completions, and follow-up appointments. Anticipated Results: Adequate participant adherence and data reliability. Aim 2: Compare clinical outcomes between patients who receive traditional care modalities versus those who added yoga to treatment plan. Methodology: Utilize validated tools such as the SRS-22 questionnaire and monitor outcomes including depression scale, sleep quality, analgesic usage, activity levels, and Cobb angle. Anticipated Results: Significant physical and psychological improvements in the yoga group.

Participants needed: 500
Trial details
Age: 10-20Biological sex: AllType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Non-operatively treated AIS patients at Johns Hopkins Hospital with back pain wh... [+3]

Scoliosis due to causes other than AIS. [+3]

Status: Recruiting

Scoliosis Survey to Development Treatment Decision Tool

This is a survey to help understand the influences related to the decision for Adolescent Idiopathic Scoliosis treatment (observation vs. bracing vs. surgery). The investigator then plans to create a decision aid to help families when making a decision about the treatment choice being presented to them.

Participants needed: 5,000
Trial details
Age: 13+Biological sex: AllType: ObservationalSponsor: Mayo ClinicUpdated: Jan 2, 2026Locations: 1
Eligibility criteria

Subject (and/or parent of subject) who has previously been treated for Adolescen...

Age less than or equal to 12 years

Status: Recruiting

Conservative Management for Adolescent Idiopathic Scoliosis

Idiopathic scoliosis is a living problem that resists correction. The underlying cause of the such disorder is unknown but directed more toward muscular disorders. However recent clinical observation showed a possible neuromuscular compromise early in those patients. The main purpose of this study is to develop a treatment procedure to correct the degree of bony curvature in patients with Idiopathic scoliosis through developing a neuromuscular corrective approach that might be a more effective conservative treatment protocol for such disorder.

Participants needed: 60
Trial details
Age: 10-17Biological sex: AllType: InterventionalSponsor: Umm Al-Qura UniversityUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Adolescents of both sexes with an age range between 10-17 years. [+5]

Adolescents with cerebral palsy or other degenerative neurological disorders; [+8]

Status: Recruiting

Erector Spinae Plane Blockade in Pediatric Scoliosis Surgery Patients

Providing effective analgesia after spinal fusion for idiopathic scoliosis remains a challenge with significant practice variation existing among high volume spine surgery centers. Even in the era of multimodal analgesia, opioids are the primary analgesics used for pain control after pediatric scoliosis surgery, but have multiple known adverse effects. The erector spinae plane block (ESPB) is a newly described fascial plane block performed by injecting local anesthetic between the erector spinae muscle and the transverse process. Additionally, there are case reports describing the ESPB as part of a multi-modal analgesic plan in adult degenerative spine surgery as well as adult spinal deformity surgery, demonstrating effective analgesia and no clinical motor blockade. Although it is known that the inflammatory reaction plays a crucial role in the mechanism of acute pain after major surgery, the effectiveness of the current regional approach on inflammatory response is not well studied.

Participants needed: 50
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: May 1, 2025Locations: 1
Eligibility criteria

ASA I-III [+2]

Thorascopic tethering procedure [+13]

Status: Recruiting

Quality of Life (HRQoL) of AIS Patients Who Require Bracing or Surgery Using SRS-22 Questionnaire

Adolescent Idiopathic Scoliosis (AIS) is an unexpected curvature of spine at teenage. AIS causes mainly unpleasant appearance, and sometime comes with pain and difficult to locate or move around. When the spinal curve, or "Cobb angle", increases with time, the investigators call it severe condition when the Cobb angle is 60 degrees or above. The severe suffering patients need to be operated to correct their spinal curve by using metallic rods and metallic screws (implants) to fix the spine. In order to avoid this surgery, the investigators use "brace", a hard fitting case, trying to control the spinal curve degree by using forces from outside. (bracing) to intervene the spinal curve progression is highly recommended for patients with particular clinical characteristics. However, bracing is not always a present experience apart from function restriction. Clinical recommendation requires the patients to brace over 20 hours everyday, which means the patients have to be "braced" around the clock. Patients' perception on being "braced" all day, apart from discomforts under bracing, self-image and mental health after bracing are also important psycho-social factors which have yet to be addressed. Based on our clinical experience, 1-2% of AIS patients, undergoing bracing or not (i.e. at observation stage), require surgical intervention due to rapid spinal progression in a short period of time. By definition, surgery will be arranged for patients with major spinal curve ≥50. The use of health-related-quality-of-life (HRQoL) questionnaires allow clinical professionals to explore many different kinds of interests on patients, including the patient's feeling on his/her medical condition and satisfaction with provided care. Scoliosis Research Society (SRS) patient outcome tool has been a well-accepted HRQoL questionnaire to look for the perception of patients with spinal problems of their status. The SRS-22 questionnaire that has been well accepted as its trustworthy on the score results and SRS-22 is good to be used in patients under different conditions across the disease. This is very important to obtain and compare the scores over time in order to look for any consistent changes. Apart from AIS patients requiring bracing, surgical cases are also very important group of patients to monitor their quality of life before and after surgery, and every follow-up visit after surgery.

Participants needed: 2,000
Trial details
Biological sex: AllType: ObservationalSponsor: Chinese University of Hong KongUpdated: Feb 12, 2025Locations: 1
Eligibility criteria

AIS patients who attend the scoliosis clinic at specialized outpatient clinic in... [+1]

To observe (i.e. not require to wear brace) after clinic visit [+1]

Status: Not yet recruiting

Study Comparing the PathKeeper System for Pedicle Screw Positioning in Spine Surgery With Traditional Care

The goal of this is to evaluate performance of the Pathkeeper Surgical System. The main question\[s\]it aims to answer are: 1) evaluate pedicle screw position Participants will in compare Experimental arm: PathKeeper System (PKS) with control arm

Participants needed: 32
Trial details
Age: 16+Biological sex: AllType: InterventionalSponsor: Deep Health Ltd.Updated: Feb 5, 2025Locations: 1
Eligibility criteria

Men and women [+3]

Men and women [+3]

Status: Not yet recruiting

Effects of Expiratory Muscle Strength Training in Adolescent Idiopathic Scoliosis

Adolescent idiopathic scoliosis result in deterioration of core muscles and respiratory system. Core muscles provide trunk stabilization as well as responsible for respiratory system. Especially tr. abdominis, rectus abdominis, external oblic and internal oblic muscle, which are core muscles, highly active during forced expiration while diaphragm muscle also active during inspiration. Thus, expiratory muscle strength training has effect not only respiratory muscle strength but also trunk stabilization. While, effects of expiratory muscle strength training in adolesecent idiopathic scoliosis is a topic that needs to be investigated, this topic has not been investigated until today. Hence, this current study aimed to investigate the effects of expiratory muscle strength training on cobb angle, respiratory muscle strength, core stabilization, functional exercise capacity and quality of life.

Participants needed: 24
Trial details
Age: 10-19Biological sex: AllType: InterventionalSponsor: Gazi UniversityUpdated: Dec 31, 2024Locations: 1
Eligibility criteria

Individuals diagnosed with idiopathic scoliosis, [+2]

Individuals who have undergone spinal surgery, [+3]

Status: Recruiting

The Role of VitD in Rehabilitation of Idiopathic Adolescent Scoliosis

The purpose of this current prospective study is to determine the role of vitamin D in the development and restoration of spinal deformities in adolescence.

Participants needed: 80
Trial details
Phase: Phase 2Age: 10-18Biological sex: AllType: InterventionalSponsor: University of IoanninaUpdated: Dec 6, 2024Locations: 2
Eligibility criteria

Idiopathic Adolescent Scoliosis [+1]

Neuromuscular diseases [+2]

Status: Recruiting

Personalized Spine Study Group (PSSG) Registry

The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.

Participants needed: 1,000
Trial details
Age: 10-85Biological sex: AllType: ObservationalSponsor: University of Colorado, DenverUpdated: Oct 3, 2024Locations: 1
Eligibility criteria

Patient has been/ will be operated and instrumented with patient-specific rod or... [+1]

Patient unable to sign an informed consent form [+4]

Status: Recruiting

Virtual Reality's Effect on Decreasing Pain and Subsequent Opioid Use in Pediatric Patients in the Post-Operative Period Following Scoliosis Repair

The goal of this study is to determine whether introducing VR in the immediate post-operative period following scoliosis repair can reduce perceived pain and stress in pediatric patients and in turn ultimately decrease opioid use. Based on previous studies that have been performed in other fields of pediatrics showing a decrease in pain and stress with VR use, the investigators hypothesize that VR will significantly decrease patient's reported level of pain and stress immediately following the VR session, and that patients will require less opioids during their inpatient stay as a result.

Participants needed: 50
Trial details
Age: 7-21Biological sex: AllType: InterventionalSponsor: Northwell HealthUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

all pediatric patients post scoliosis repair [+1]

age less than 7 years; [+4]

Status: Recruiting

Massage Therapy After Thoracic or Lumbar Surgery

The purpose of this research is to look at the effect of massage therapy on the pain, anxiety, and quality of life that pediatric patients have after undergoing spinal fusion surgery. This is a single-site, prospective, randomized, interventional study design that will involve post-thoracic and post-lumbar spinal fusion surgeries of pediatric patients from 7 to 19 years of age that present to Cook Children's Medical Center in Fort Worth, Texas. These patients will be identified prior to their scheduled spinal fusion surgery and recruited to enroll in the study. The planned spinal fusion surgeries are not considered part of this research project, but rather considered standard of care and would occur whether the patient is enrolled in this project or not. Enrolled participants will be followed during their inpatient stay and through their subsequent follow-up visits at weeks 2, 6, and 12. Participants will be randomly assigned to either a massage therapy group or a group that receives the standard (normal) care for recovery after surgery. The final study involvement will occur at week 16 (post-hospital discharge) where a study team member will administer a quality of life (PedsQL) questionnaire via phone or mail with the subject. Data will be collected after study related procedures are completed.

Participants needed: 100
Trial details
Age: 7-19Biological sex: AllType: InterventionalSponsor: Cook Children's Health Care SystemUpdated: May 23, 2024Locations: 1
Eligibility criteria

Patients scheduled to undergo their first thoracic or lumbar spinal fusion surge... [+3]

Prospective patients scheduled to undergo any spinal fusion other than a thoraci... [+13]

Status: Recruiting

Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis

The study population concerns adolescent patients with idiopathic scoliosis which requires surgical management and who have a longer waiting period of 6 months. The aim of this study is to research the predictive factors of an improvement in the quality of life of adolescents who have had surgery.

Participants needed: 866
Trial details
Age: 12-20Biological sex: AllType: ObservationalSponsor: ElsanUpdated: Feb 29, 2024Locations: 1
Eligibility criteria

Patient between 12 and 20 years old [+3]

Patient over 20 years old [+2]