- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03524027
Vertebral Column Resection (VCR) in Congenital Kyphoscoliosis (CKS)
Posterior Vertebral Column Resection (PVCR) for Correction of Adolescent Thoracolumbar Congenital Kyphoscoliosis (CKS)
Congenital spinal deformities (CSD) are caused by early embryologic errors in vertebral column formation. Spinal cord malformations are present in approximately one third of patients, even associated cardiac, renal, and genitourinary organ system anomalies in more than half of patients. Functional activity and health-related quality of life (HRQOL) are severely affected in adolescents with neglected severe congenital kyphoscoliosis (CKS) progressive curves in developing countries.
Different strategies are described with two main principles; I- Prophylactic surgeries like hemi-epiphysiodesis or in situ fusions that will cease worsening or allow progressive correction over time, II- Corrective surgeries like reconstructive osteotomies and spinal fusion with or without spinal resection. The perfect show in management of congenital spinal deformities is to pick up the curves at early stages where a prophylactic treatment can be achieved with minimal risk to the spinal cord, but certainly many cases are quite aggressive or come late enough where corrective surgeries and even spinal column resection is the only valid plan.
A posterior-based vertebral column resection (VCR) is considered to be the preferred approach in the treatment of rigid, severe, and complex spinal deformities, however the difficult and lengthy nature of the procedure require assistance from experienced and well trained team. It is relatively safe but challenging technique, that allows for dramatic radiographic correction and clinical improvement. It also carries a complication rate of 10.2% as profound blood loss, iatrogenic neurological deficit and late junctional kyphosis.
Study Overview
Status
Intervention / Treatment
Detailed Description
Preoperative Details :
Every patient is examined for 1- Shoulder balance 2- Pelvic balance 3- Thoracic hump 4- Neurological examination. Also preoperative whole-spine X-ray anteroposterior and lateral view radiographs in erect position are obtained for accurate preoperative planning. Three-dimensional Multi-Slice Computed Tomography (MSCT) scan is obtained to delineate posterior vertebral column pathoanatomy before surgery. Whole-spine MRI is obtained for declaration of any associated spinal cord malformation.
Operative Details :
Appropriate patient positioning on the operating frame to avoid excessive pressure points in the axilla, allow the abdomen to hang free, and to maintain stability of the trunk during surgery. Standard posterior exposure is performed, and pedicle screws are placed using a free-hand technique as. The exposure at the osteotomy site is extended laterally to resect a portion of the medial ribs to enhance the exposure of the vertebral body to be removed.
Once adequate exposure is achieved, a wide laminectomy is completed from the pedicles of the proximal vertebra to the pedicles of the distal vertebra. Use of tranexamic acid to minimize osseous bleeding during these lengthy surgeries is advisable. At this point, a short rod is placed into the pedicle screws of 1 side to include at least 2 pedicle screws proximally and 2 pedicle screws distally, to provide stability during the osteotomy. Once this rod is secured, the proximal and distal discs are removed and the vertebra to be removed is outlined.
Then, the osteotomy is started from the pedicle on the contralateral side, and extending into the body. The exiting nerve roots are tied and transected at the thoracic levels, gently retracted at the lumbar levels. The removal of vertebral body is proceeded using Kerrison rongeurs and osteotomes as necessary. After adequate removal, another rod is placed to the already osteotomized side, and secured. At this point the rod on the other side can be removed or kept in place, depending on the amount of expected instability.
The resection carried similarly on the contralateral side. The posterior wall of the vertebral body is kept intact until the very end of the osteotomy. After the removal of the vertebral body and discs, using a reverse cutting curette the posterior wall is fractured with anteriorly directed blows and removed using rongeurs. The endplates of the neighboring vertebrae are cleaned off of any remaining cartilage to expose bone surfaces to achieve fusion.
The anterior defect is augmented with morsellized cancellous graft with or without the use of a titanium mesh cage, depending on the width of the void. After the completion of resection, deformity correction is carried out and the posterior instrumentation system is secured using pedicle screws. Application of Wakeup test to detect any on-table neurology. Decortication followed by addition of remaining autograft and allograft to the fusion is performed. Posterior wound closure is performed over a drain.
Postoperative Details :
Follow-up protocol is carried out after 2 weeks, 3 months, 1 year, and 2 years postoperatively with whole-spine X-Ray radiographs in erect position, and after 1 year with Multi-Slice Computed Tomography (MSCT) scan to assess fusion rate.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ahmed Shawky
- Phone Number: +201010212222
- Email: ahsh313@yahoo.com
Study Contact Backup
- Name: Muhammad Almessry
- Phone Number: +201007262147
- Email: dr.muhammad.orthospine@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Neglected congenital kyphoscoliotic spinal deformity
- Thoracic and Lumbar curves only
- Age more than 10 years old
Exclusion Criteria:
- Cervical and Sacral deformities
- Revision failed back surgeries
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Congenital Thoracolumbar Kyphoscoliosis
Correction of Adolescent Thoracolumbar Congenital Kyphoscoliosis (CKS) Spinal Deformity by Posterior Vertebral Column Resection (PVCR) Surgical Technique
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Posterior Vertebral Column Resection (PVCR) Surgical Technique for Correction of Adolescent Thoracolumbar Congenital Kyphoscoliosis (CKS) Spinal Deformity
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Scoliosis Research Society (SRS)-24 (arabic version) Health-related quality of life questionnaire
Time Frame: Baseline preoperative, then 3 months, and 1 year postoperative
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The score of questionnaire components is used to assess how patients are doing regarding their function (day to day activities), their pain level (or hopefully improvement in/lack of), how they feel they look, how they feel about themselves, and if they are satisfied as the result of their treatment.
Preoperative and postoperative scores are compared.
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Baseline preoperative, then 3 months, and 1 year postoperative
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Oswestry Disability Index (ODI)
Time Frame: Baseline preoperative, then 3 months, and 1 year postoperative
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Is an index derived from the Oswestry Low Back Pain Questionnaire used by clinicians and researchers to quantify disability for low back pain.
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Baseline preoperative, then 3 months, and 1 year postoperative
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Short Form (SF)-36 Health Survey
Time Frame: Baseline preoperative, then 3 months, and 1 year postoperative
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Is widely validated and popularly used in assessing the subjective quality of life (QOL) of patients and the general public.
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Baseline preoperative, then 3 months, and 1 year postoperative
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Complications Rate
Time Frame: Intraoperative, then Immediate, 2 weeks, 3 months, and 1 year postoperative
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As neurological deficit, vascular injury, deep infection, visual affection, pulmonary embolism, pleural effusion, deep venous thrombosis, implant-related problems, proximal junctional kyphosis, and re-operation for any cause.
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Intraoperative, then Immediate, 2 weeks, 3 months, and 1 year postoperative
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American Spinal Injury Association (ASIA) Score
Time Frame: Baseline preoperative, then immediate, and 3 months postoperative
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A score developed by the American Spinal Injury Association for essential minimal elements of neurologic assessment for all patients with a spinal injury.
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Baseline preoperative, then immediate, and 3 months postoperative
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Local Kyphosis Angle (LKA)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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Assessed on the lateral radiograph by measuring the angle obtained by a line parallel to the inferior endplate of the deformed vertebra and that of the vertebra one level above.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Lumbar Lordosis Angle (LLA)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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Angle measured between L1 and L5 lower end plates.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Thoracic Kyphosis Angle (TKA)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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Angle measured between T1 and T12 lower end plates.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Sagittal Vertical Axis (SVA) to C7 Plumb Line (C7PL)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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To quantify global alignment.
It is defined as the sagittal offset of a plumb line dropped from the C7 vertebral body from the posterosuperior corner of the sacral plate.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Scoliosis Angle (Cobb's Angle)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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To measure and quantify the magnitude of spinal deformities, especially in the case of scoliosis.
The Cobb angle measurement is the "gold standard" of scoliosis evaluation endorsed by Scoliosis Research Society.
It is used as the standard measurement to quantify and track the progression of scoliosis.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Shoulder Balance (Clavicle Angle)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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It is the angle that is subtended between a horizontal reference line - clavicle horizontal reference line (CHRL), which is drawn perpendicular to the lateral edge of the radiograph and touches the most cephalad portion of the elevated clavicle and a line which touches the most cephalad aspect of both the right and left clavicles - clavicle reference line (CRL).
By convention, angles subtended with the left shoulder up are positive and angles subtended with the right shoulder up are negative (consistent with directionality of the T1 tilt angle).
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Central Sacral Vertical Line (CSVL) to C7 Plumb Line (C7PL)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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Coronal decompensation is measured as the horizontal distance between a plumb line dropped downward from the center of the C7 (C7PL) vertebral body and the central sacral vertical line (CSVL), which is a line drawn vertically through the center of the sacrum.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Body Height (BH)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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The height is measured using a measuring tape with patient standing without shoes.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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T1-S1 Trunk Height (TH)
Time Frame: Baseline preoperative, then 2 weeks, and 1 year postoperative
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The T1-S1 height of the spine and the T1-S1 length of the spine are measured and compared.
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Baseline preoperative, then 2 weeks, and 1 year postoperative
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Leg Length Discrepancy (LLD)
Time Frame: Baseline preoperative, then 1 year postoperative
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Radiographic measurement of difference between the lengths of the legs.
Full-length standing anteroposterior radiograph compared with scanogram.
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Baseline preoperative, then 1 year postoperative
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CT-based Classification for assessment of biological graft fusion
Time Frame: 1 year postoperative
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A new assessment method of bony union using high-speed spiral CT imaging is proposed which reflects the gradually increasing biological stability of the construct.
Grade I (complete fusion) implies cortical union of the allograft and central trabecular continuity.
Grade II (partial fusion) implies cortical union of the structural allograft with partial trabecular incorporation.
Grade III (unipolar pseudarthrosis) denotes superior or inferior cortical non-union of the central allograft with partial trabecular discontinuity centrally and Grade IV (bipolar pseudarthrosis) suggests both superior and inferior cortical non-union with a complete lack of central trabecular continuity.
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1 year postoperative
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Mohamed El-Meshtawy, Assiut University
- Principal Investigator: Belal Elnady, Assiut University
Publications and helpful links
General Publications
- Aydogan M, Ozturk C, Tezer M, Mirzanli C, Karatoprak O, Hamzaoglu A. Posterior vertebrectomy in kyphosis, scoliosis and kyphoscoliosis due to hemivertebra. J Pediatr Orthop B. 2008 Jan;17(1):33-7. doi: 10.1097/01.bpb.0000218031.75557.f0.
- Lenke LG, O'Leary PT, Bridwell KH, Sides BA, Koester LA, Blanke KM. Posterior vertebral column resection for severe pediatric deformity: minimum two-year follow-up of thirty-five consecutive patients. Spine (Phila Pa 1976). 2009 Sep 15;34(20):2213-21. doi: 10.1097/BRS.0b013e3181b53cba.
- Ayvaz M, Akalan N, Yazici M, Alanay A, Acaroglu RE. Is it necessary to operate all split cord malformations before corrective surgery for patients with congenital spinal deformities? Spine (Phila Pa 1976). 2009 Oct 15;34(22):2413-8. doi: 10.1097/BRS.0b013e3181b9c61b.
- Ruf M, Jensen R, Letko L, Harms J. Hemivertebra resection and osteotomies in congenital spine deformity. Spine (Phila Pa 1976). 2009 Aug 1;34(17):1791-9. doi: 10.1097/BRS.0b013e3181ab6290.
- Hedequist D, Emans J. Congenital scoliosis. J Am Acad Orthop Surg. 2004 Jul-Aug;12(4):266-75. doi: 10.5435/00124635-200407000-00007.
- Soliman HAG. Health-related Quality of Life of Adolescents With Severe Untreated Congenital Kyphosis and Kyphoscoliosis in a Developing Country. Spine (Phila Pa 1976). 2018 Aug;43(16):E942-E948. doi: 10.1097/BRS.0000000000002598.
- Wang Y, Lenke LG. Vertebral column decancellation for the management of sharp angular spinal deformity. Eur Spine J. 2011 Oct;20(10):1703-10. doi: 10.1007/s00586-011-1771-0. Epub 2011 Mar 19.
- Lenke LG, Shaffrey CI, Carreon LY, Cheung KMC, Dahl BT, Fehlings MG, Ames CP, Boachie-Adjei O, Dekutoski MB, Kebaish KM, Lewis SJ, Matsuyama Y, Mehdian H, Pellise F, Qiu Y, Schwab FJ; AO Spine International and SRS Scoli-RISK-1 Study Group. Lower Extremity Motor Function Following Complex Adult Spinal Deformity Surgery: Two-Year Follow-up in the Scoli-RISK-1 Prospective, Multicenter, International Study. J Bone Joint Surg Am. 2018 Apr 18;100(8):656-665. doi: 10.2106/JBJS.17.00575.
- Lenke LG, Sides BA, Koester LA, Hensley M, Blanke KM. Vertebral column resection for the treatment of severe spinal deformity. Clin Orthop Relat Res. 2010 Mar;468(3):687-99. doi: 10.1007/s11999-009-1037-x. Epub 2009 Sep 1.
- Lenke LG, Newton PO, Sucato DJ, Shufflebarger HL, Emans JB, Sponseller PD, Shah SA, Sides BA, Blanke KM. Complications after 147 consecutive vertebral column resections for severe pediatric spinal deformity: a multicenter analysis. Spine (Phila Pa 1976). 2013 Jan 15;38(2):119-32. doi: 10.1097/BRS.0b013e318269fab1.
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PVCR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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