The Tether™ - Vertebral Body Tethering System Post Approval Study

Scoliosis Idiopathic Clinical Trial

Official title:

The Tether™ - Vertebral Body Tethering System Post Approval Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04505579
• Other study ID #: RAU2019-40S
• Status: Recruiting
• Start date: October 29, 2020
• Est. completion date: December 31, 2027

Study information

• Verified date: February 2024
• Source: ZimVie
• Contact: Monica Barascout, BS
• Phone: 1-303-465-8960
• Email: Monica.Barascout[@]zimvie.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

This study is an opportunity to provide continued reasonable assurance of the safety and probable benefit of The Tether HUD. The study will collect long term safety and efficacy information from patients who have had their idiopathic scoliosis treated via anterior vertebral body tethering (AVBT) with The Tether.

Description:

While spinal fusion remains the standard surgical treatment for progressive idiopathic scoliosis, concerns about the long-term effects of spinal fusion have led to the investigation of growth-modulation techniques. Anterior Vertebral Body Tethering (AVBT) is one such technique that utilizes growth modulation to remodel the shape of the vertebra and straighten scoliotic curves in skeletally immature individuals. In this technique, screws are inserted at each vertebral level for the length of the convex side of the curve. A strong cord is connected through the screw tulip heads and used to initially straighten the curve as each level is fixed with a set screw. Following surgery and during the growth period the spine begins to remodel according to the Hueter-Volkmann Law, bone growth is relatively inhibited in areas of increased pressure (convex or tethered side) and relatively stimulated in areas of decreased pressure or tension (concave side). Following this principle, AVBT has been shown to alter spinal growth with the potential to correct scoliosis while maintaining spine flexibility.

The objective of the study is to assess the ongoing safety and probable benefit of The Tether HUD which was approved by the FDA under an HDE. Subject enrollment and data collection will be managed by the Harms Study Group (HSG) and Setting Scoliosis Straight Foundation (SSSF) Registry. Institutions that are HSG members or affiliates, with Investigators/surgeons that are trained and approved to perform surgeries with The Tether, will participate in the registry. Ten sites from this group will be identified as study sites specific to this Tether post-approval study (PAS). Consecutive subjects from these sites, that meet the eligibility criteria of this study, will be flagged in the registry as the PAS cohort and the study endpoints will be assessed across this population.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: December 31, 2027
• Est. primary completion date: August 31, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Diagnosis of progressive idiopathic scoliosis

• Skeletally immature, based on both Risser (<5) and Sanders (<8) assessments

• Major Cobb angle =30° and =65°

• Osseous structure dimensionally adequate to accommodate screw fixation, as determined by radiographic imaging

• Failed or intolerant to bracing

Exclusion Criteria:

• Presence of any systemic infection, local infection, or skin compromise at the surgical site

• Prior spinal surgery at the level(s) to be treated

• Documented poor bone quality, defined as a T-score -1.5 or less

• Any other medical or surgical condition which would preclude the potential benefit of spinal surgery, such as coagulation disorders, allergies to the implant materials, and patient's unwillingness or inability to cooperate with post-operative care instructions

• Unwillingness, inability, or living situation (e.g. custody arrangements, homelessness, detention) that would preclude ability to return to the study site for follow-up visits as described in protocol and Informed Consent

• Unwillingness to sign Informed Consent Form and participate in study procedures

Related Conditions & MeSH terms

• Scoliosis
• Scoliosis Idiopathic

Intervention

Device:
• Anterior Vertebral Body Tethering
Anterior Vertebral Body Tethering (AVBT) is a technique that utilizes growth modulation to remodel the shape of the vertebra and straighten scoliotic curves in skeletally immature individuals. In this technique, screws are inserted at each vertebral level for the length of the convex side of the curve. A strong cord is connected through the screw tulip heads and used to initially straighten the curve as each level is fixed with a set screw. Following surgery and during the growth period the spine begins to remodel according to the Hueter-Volkmann Law, bone growth is relatively inhibited in areas of increased pressure (convex or tethered side) and relatively stimulated in areas of decreased pressure or tension (concave side).

Locations

Country	Name	City	State
United States	Children's Healthcare of Atlanta	Atlanta	Georgia
United States	Children's Hospital Colorado	Aurora	Colorado
United States	University of Missouri - Columbia	Columbia	Missouri
United States	Nemours Children's Health	Jacksonville	Florida
United States	Ochsner Health	New Orleans	Louisiana
United States	Mount Sinai	New York	New York
United States	Shriners Children's Hopital	Philadelphia	Pennsylvania
United States	Mayo Clinic	Rochester	Minnesota
United States	Rady Children's Hospital	San Diego	California
United States	Seattle Children's	Seattle	Washington

Sponsors (3)

Lead Sponsor	Collaborator
ZimVie	Exponent, Inc., Setting Scoliosis Straight Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of SAEs and device- &/or procedure-related AEs	The primary safety endpoint is the rate of Serious Adverse Events (SAEs) and device- and/or procedure-related Adverse Events (AEs)	AVBT surgery to five year post-op
Primary	Percentage of subjects with maintenance of the major Cobb angle less than or equal to 40 degrees at 60 months post-surgery	The primary probable benefit endpoint is the percentage of patients with maintenance of the major Cobb angle less than or equal to 40 degrees at 60 months post-surgery	AVBT surgery to five year post-op
Secondary	Adverse Events	Rates of overall Adverse Events; relatedness, severity, time to event	AVBT surgery to five year post-op
Secondary	Reoperation	Rates and types of reoperation	AVBT surgery to five year post-op
Secondary	Number of participants with new curves that develop above or below the tethered portion of the spine.	Determined by radiographic assessment, defined as a new curve development with Cobb angle measurement greater than or equal to 40 degrees.	AVBT surgery to five year post-op
Secondary	Number of participants with secondary curves that progress to the point of clinical significance.	Determined by radiographic assessment, typically defined as an increase in secondary Cobb angle measurement greater than or equal to 10 degrees, or medical intervention/ intent to treat.	AVBT surgery to five year post-op
Secondary	Number of participants with device integrity failures including cord breakage and screw migration.		AVBT surgery to five year post-op
Secondary	Mean (SD) and distributions of sagittal balance (mm) from pre-op through last visit	Sagittal balance is assessed on the lateral radiograph by measuring the difference (i.e. distance) between posterosuperior aspect of the S1 vertebral body and the plumb line.	Baseline to five year post-op
Secondary	Mean (SD) and distributions of lumbar lordosis (degrees) from pre-op through last visit.	Lumbar lordosis is defined as the angle at the intersection of lines perpendicular to lines parallel to the superior endplate of T12 and the superior endplate of S1.	Baseline to five year post-op
Secondary	Mean score of Scoliosis Research Society 22r Patient Questionnaire	Self-reported outcomes of function, pain, self-image, mental health, and satisfaction. Mean score; 5 (Best) - 1 (Worst)	Baseline to five year post-op
Secondary	Number of participants with compromised lung function	Comparison of the measured lung function (forced expiratory volume (FEV1), forced vital capacity (FVC) and FEV1/FVC) to predicted values, lower and upper limits of normal to determine if lung function is within the limits of the normal population.	Baseline to five year post-op
Secondary	Measurement (degrees rotation) of trunk shape by scoliometer device. Mean (SD) [min, max] will be reported.	Measurements of trunk shape or rib hump will be collected preoperatively and at each follow-up visit. A standard scoliometer device will be used to measure the rib hump in the thoracic and/or lumbar regions of the spine, as applicable. The scoliometer is laid across the curve at right angles with the 0° mark at the spinous process and resting gently on the skin, not pressed down. The degrees of rotation are read and recorded.	Baseline to five year post-op
Secondary	Trunk flexibility as determined by distance (cm) of flexion and lateral bend using fingertip to floor method.		Baseline to five year post-op