Trial · NCT07905573
MALMOS Technique for Selected Subaxial Cervical Spine Fractures
NCT07905573, Not applicable, Not yet recruiting, Assiut University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. MALMOS Technique for Selected Subaxial Cervical Spine Fractures. Trials, record NCT07905573. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07905573
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- MALMOS Technique for Selected Subaxial Cervical Spine Fractures
- NCT number
- NCT07905573
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 15 participants, estimated
- Lead sponsor
- Assiut University
- Conditions
- Cervical Spine Fractures
- Interventions
- Meshtawy's Anterior Ligamentotaxis and Miniplate Osteosynthesis (MALMOS) Technique With Neutralization H-Plate Fixation
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Segmental Cobb Angle (Degrees) | Preoperatively, immediately postoperatively, and through 6 months postoperatively or until CT-confirmed fracture healing, whichever occurs first. | Change in segmental Cobb angle from the immediate postoperative measurement to the final assessment at CT-confirmed fracture healing. |
| Secondary | Vertebral Body Height (precentage) | Preoperatively, immediately postoperatively, and through 6 months postoperatively or until CT-confirmed fracture healing, whichever occurs first. | Change in anterior and posterior vertebral body height from the immediate postoperative assessment to the final radiological assessment. |
| Secondary | Pain Intensity (Visual Analog Scale Score) | through study completion, an average of 6 months | Visual Analog Scale for Neck Pain (VAS): Scores range from 0 to 10, with higher scores indicating greater pain and a worse outcome. |
| Secondary | Neck Disability | through study completion, an average of 6 months | Neck Disability Index (NDI): Total scores range from 0 to 50, with higher scores indicating greater neck-related disability and a worse outcome. |
| Secondary | Neurological Status | through study completion, an average of 6 months | American Spinal Injury Association (ASIA) Impairment Scale (AIS): Grades range from A to E, with Grade A indicating a complete spinal cord injury and Grade E indicating normal sensory and motor function. Higher grades indicate better neurological function and a better outcome. |
| Secondary | Complications | through study completion, an average of 6 months | Incidence of perioperative and postoperative complications |
| Secondary | Secondary Surgery | through study completion, an average of 6 months | Incidence of Secondary Surgery |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers7
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07905573
GET https://conductscience.org/api/trials/v1/NCT07905573/registered