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X-ray Evaluation of the Effectiveness of the Atlas Correction in Patients With Chronic Subluxation of the Atlas

X-ray Assessment of the Effectiveness of Hardware Medical Acupressure of the Suboccipital Muscles According to the Atlas-Standard Method in Patients With Chronic Subluxation of the First Cervical Vertebra

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05986656
Acronym
AtlaStandard
Enrollment
46
Registered
2023-08-14
Start date
2023-09-08
Completion date
2024-07-14
Last updated
2024-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subluxation and Dislocation of C0/C1 Cervical Vertebrae

Brief summary

The aim of the study is to evaluate the effect of the procedure of medical acupressure of the suboccipital muscles according to the Atlas-Standard method on the normalization of the position of the first cervical vertebra and the angles of the spinal column in patients with diagnosed chronic subluxation with objectification of the results by radiography and inclinometry.

Interventions

PROCEDUREAtlas-Standard method

Hardware acupressure of the suboccipital muscles according to the Atlas-Standard method for the reduction of chronic subluxation of the first cervical vertebra.

Sponsors

Clinic of Phlebology and Laser Surgery, Chelyabinsk, Russia
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients with chronic subluxation of the first cervical vertebra with complaints of pain in the occiput/cervical/thoracic/lumbar spine/limitation of head rotation in one or both directions. * Scoliotic deformity of the spine 1-2 degrees.

Exclusion criteria

* Pregnancy * Fractures of the first / second cervical vertebra in history * Fractures of the spine in any of the departments in the anmenesis * Assimilation of the atlas with the occipital bone or the second cervical vertebra * Operations on the spine using metal structures * Scoliosis 3-4 degree * Botulinum toxin injections in the suboccipital region within the last year * Taking muscle relaxants * Corrective surgery on muscles and bones * Braces * Active period of dental implants installation * Postoperative period (any operation, including on the eyes) less than 6 months * Acute infectious diseases - less than 2 weeks from the start of recovery * Skin diseases with inflammatory manifestations in the neck * Oncological diseases * Recovery period after injury (cervical and brain injury) or stroke less than a year * Established mental illness * Extreme malnutrition (cachexia)

Design outcomes

Primary

MeasureTime frameDescription
Distance between righr and left inner surface of the lateral mass of the atlas and the outer surface of the odontoid process of the axis on x-ray1 month.Elimination of asymmetry between the right and left atlantodental intervals

Secondary

MeasureTime frameDescription
Pain level6 monthChange in the pain level in the spine according to VAS (Visual Analog Scale from 0 to 10 where 0 is no pain, 10 is worst pain imaginable)
Painkillers6 monthNumber of participants who use painkillers before and after procedure
The functional disability6 monthEvaluated with the Oswestry Disability Index (ODI: 0 = minimal \[better outcome\] to 100% = maximal disability \[worse outcome\])
Changes in the angles of deviation of the spinous processes6 monthMeasurement of the angles of deviation of the spinous processes in degrees of the frontal and sagittal cavities from C7 to S3 in the position of full flexion, extension of the spine and in the vertical position measured by Spinal Mouse device
Changes in the range of motion of the spine6 monthChanges in the range of motion of the spine in degrees in the frontal and sagittal planes in the range from C7 to S3 in the position of full flexion and extension of the spine measured by Spinal Mouse device

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026