ClinicalTrials.gg
Status unknownNCT05479864Updated Jul 29, 2022

Single Level Anterior Cervical Corpectomy Without Posterior Stabilization

An interventional study of anterior cervical corpectomy and fusion in Cervical Spine Fusion, sponsored by Assiut University. Status unknown. Per ClinicalTrials.gov, last updated 2022-07-29.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Sex
All
01

Study summary

evaluate and assess short term outcome of treating degenerative and non-degenerative cervical conditions with single level anterior cervical corpectomy without posterior fusion

Read the detailed description

Cervical corpectomy is a procedure that removes damaged vertebrae and intervertebral disc that are compressing the spinal cord and spinal nerves. Various graft materials or spacers are used to maintain height and stability followed by anterior plating. It has an important role in the management of various degenerative, traumatic, neoplastic and infectious disorders of cervical spine.

While ACCF effectively decompresses the spinal cord, it is debated whether it can provide enough cervical stability, or an additional posterior fixation (PF) is required. Studies show that in multi-level anterior cervical corpectomy, additional posterior fixation provides extra support to improve cervical stability whether it is performed initially, or later as a supplementary surgery if material failure or instability occurred, On the other hand, in single level corpectomy, it remains controversial as single level ACCF showed sufficient stability in the majority of cases without additional support but pathologies affecting bone quality like infections and neoplasms seemed to be risk factor for construct failure and instability so additional PF was required .

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Conditions studied

  • Cervical Spine Fusion
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In context

Lead sponsor

Assiut University is the lead sponsor of 5,050 studies on the registry; 2,174 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

- All patients with degenerative and non-degenerative cervical conditions (trauma, tumors and infections) treated with "single level anterior cervical corpectomy without posterior fusion

Exclusion criteria

Exclusion Criteria:

  • Patients who refuse to participate in the study
  • Patients who are not available for 6 months follow up
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Other
    Anterior cervical corpectomy and fusion

    removal of damaged vertebrae and intervertebral disc that are compressing the spinal cord and spinal nerves. Various graft materials or spacers are used to maintain height and stability followed by anterior plating

    Procedure: anterior cervical corpectomy and fusion

Interventions

  • Procedureanterior cervical corpectomy and fusion

    removal of damaged vertebrae and intervertebral disc that are compressing the spinal cord and spinal nerves

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What researchers measure

Primary outcomes

  1. Radiological parameter

    * Bony fusion with no metal failure * presence of trabecular bridging and/or absence of motion

    Time frame: Baseline

Secondary outcomes

  1. Physiological parameter

    Percentage of improvement in NDI following surgical treatment during the follow up visits

    Time frame: baseline

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Nouri A, Tetreault L, Singh A, Karadimas SK, Fehlings MG. Degenerative Cervical Myelopathy: Epidemiology, Genetics, and Pathogenesis. Spine (Phila Pa 1976). 2015 Jun 15;40(12):E675-93. doi: 10.1097/BRS.0000000000000913. PubMed 25839387 ↗
  • Perez-Cruet MJ, Samartzis D, Fessler RG. Anterior cervical discectomy and corpectomy. Neurosurgery. 2006 Apr;58(4 Suppl 2):ONS-355-9; discussion ONS-359. doi: 10.1227/01.NEU.0000205285.20336.C2. PubMed 16582660 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05479864
Lead sponsor
Assiut University
Responsible party
Ahmed Ragab Hassan Alshemy (Principal investigator, Assiut University) — Principal investigator
First posted
Jul 29, 2022
Start date
Aug 2022 (estimated)
Primary completion
Apr 2023 (estimated)
Completion
Apr 2023 (estimated)
Last update
Jul 29, 2022

Study contacts

ahmed alshemy
Contact
ahmedalshemy10@med.aun.edu.eg
01019197672

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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