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Corrective Spinal Surgery for Severe Spinal Curvature in People With Ankylosing Spondylitis

NCT07930611, Not applicable, Not yet recruiting, China-Japan Friendship Hospital

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleCorrective Spinal Surgery for Severe Spinal Curvature in People With Ankylosing SpondylitisClinicalTrials.gov
NCT numberNCT07930611ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment35 participants, estimatedClinicalTrials.gov
Lead sponsorChina-Japan Friendship HospitalClinicalTrials.gov
ConditionsAnkylosing SpondylitisClinicalTrials.gov
Interventionspedicle subtraction osteotomyClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 33

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in Bath Ankylosing Spondylitis Functional Index(BASFI) from baseline to 12 months after surgery (ΔBASFI)at baseline, 6 months, and 12 monthson the 0-10 scale. A negative change indicates improved function.ClinicalTrials.gov
PrimaryChange in T1 pelvic angle (TPA) from baseline to 12 months after surgery (ΔTPA)at baseline, 6 months, and 12 months
TPA will be measured on the standing lateral full-spine radiograph as the angle between the line connecting the center of the T1 vertebral body to the bicoxofemoral axis and the line connecting the bicoxofemoral axis to the midpoint of the superior endplate of S1. TPA incorporates both global spinal inclination and pelvic retroversion and provides a global measure of sagittal alignment. A negative change indicates improved function.
ClinicalTrials.gov
Secondarythe seventh cervical vertebra (C7)-sagittal vertical axis(SVA)at baseline, 6 months, and 12 monthsMeasured on a full-length standing lateral radiograph as the horizontal distance from the C7 plumb line to the posterior-superior corner of the S1 endplate. Unit: millimeters (mm)ClinicalTrials.gov
Secondaryspinosacral angle(SSA)at baseline, 6 months, and 12 monthsMeasured as the angle between the C7 plumb line and the sacral endplate line. Unit: degrees (°)ClinicalTrials.gov
SecondarySagittal Pelvic Angle(SPA)at baseline, 6 months, and 12 monthsMeasured as the angle between the sacral endplate line and the line connecting the femoral head axis to the C7 plumb line. Unit: degrees (°)ClinicalTrials.gov
Secondarypelvic incidence(PI)at baseline, 6 months, and 12 monthsMeasured as the angle between the line perpendicular to the sacral endplate at its midpoint and the line from that midpoint to the femoral head axis. Unit: degrees (°)ClinicalTrials.gov
Secondarypelvic tilt(PT)at baseline, 6 months, and 12 monthsMeasured as the angle between the vertical line and the line from the femoral head axis to the sacral endplate midpoint. Unit: degrees (°)ClinicalTrials.gov
Secondarysacral slope(SS)at baseline, 6 months, and 12 monthsMeasured as the angle between the sacral endplate line and the horizontal line. Unit: degrees (°)ClinicalTrials.gov
SecondaryPelvic Incidence(PI)-lumbar lordosis(LL) mismatchat baseline, 6 months, and 12 monthsCalculated as PI minus LL. Unit: degrees (°)ClinicalTrials.gov
Secondaryglobal kyphosis(GK)at baseline, 6 months, and 12 monthsMeasured as the angle between the superior endplate of the upper-most tilted vertebra and the inferior endplate of the lower-most tilted vertebra in the kyphotic segment. Unit: degrees (°)ClinicalTrials.gov
Secondarythoracic kyphosis(TK)at baseline, 6 months, and 12 monthsMeasured as the Cobb angle between the superior endplate of T4 and the inferior endplate of T12. Unit: degrees (°)ClinicalTrials.gov
Secondaryoracolumbar kyphosis(TLK)at baseline, 6 months, and 12 monthsMeasured as the Cobb angle between the superior endplate of T10 and the inferior endplate of L2. Unit: degrees (°)ClinicalTrials.gov
Secondarylumbar lordosis(LL)at baseline, 6 months, and 12 monthsMeasured as the Cobb angle between the superior endplate of L1 and the superior endplate of S1. Unit: degrees (°)ClinicalTrials.gov
SecondaryKyphosis apex vertebraat baseline, 6 months, and 12 monthsIdentified as the vertebra at the apex of the maximal kyphotic curve on the lateral radiograph. Unit: vertebral level (e.g.T8, T9)ClinicalTrials.gov
SecondaryLocal osteotomy angleat baseline, 6 months, and 12 monthsMeasured as the angle created at the osteotomy site between the superior and inferior endplates of the resected/adjacent vertebrae on intraoperative or postoperative imaging. Unit: degrees (°)ClinicalTrials.gov
Secondarythe second cervical vertebra(C2)-the seventh cervical vertebra(C7) lordosis.at baseline, 6 months, and 12 monthsMeasured as the Cobb angle between the inferior endplate of C2 and the inferior endplate of C7. Unit: degrees (°)ClinicalTrials.gov
Secondarythe second cervical vertebra(C2)-the seventh cervical vertebra(C7) sagittal vertical axis(SVA)at baseline, 6 months, and 12 monthsMeasured as the horizontal distance from the C2 plumb line (vertical line from the C2 centroid) to the posterior-superior corner of C7. Unit: millimeters (mm)ClinicalTrials.gov
Secondarythe first thoracic vertebra(T1) slopeat baseline, 6 months, and 12 monthsMeasured as the angle between the superior endplate of T1 and the horizontal line. Unit: degrees (°)ClinicalTrials.gov
Secondarythe first thoracic vertebra(T1) angleat baseline, 6 months, and 12 monthsT1 angle measured between the T1 endplate line and the line from the T1 centroid to the C7 centroid. Unit: degrees (°)ClinicalTrials.gov
SecondaryNeck tiltat baseline, 6 months, and 12 monthsNeck tilt measured as the angle between the vertical line and the line from the sternal notch to the T1 centroidClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.