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EuroPainClinicsStudy X

EuroPainClinicsStudy X (Minimally Invasive Spinal Surgical Approaches)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04855682
Acronym
EPCS X
Enrollment
180
Registered
2021-04-22
Start date
2021-07-15
Completion date
2024-04-15
Last updated
2021-05-26

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

Conditions

Back Pain

Brief summary

Non-interventional, retrospective-prospective cohort study based on the collection of data and their evaluation after medical procedures: micro-discectomy, endoscopic discectomy, and hemilaminectomy.

Detailed description

The aim of this clinical study is to compare the benefits and complications after minimally invasive spinal procedures in patients with acute lumbosacral radicular syndrome caused by a herniated disc compressing the spinal neural structures. The study only works with patient data provided by the outpatient clinic for research analysis in the EPCS IV clinical study. All patient data are encrypted during collection and evaluation during the study, and stored in an encrypted database. The data will be evaluated by an independent institution - The Institute of Measurement of the Slovak Academy of Sciences.

Interventions

OTHERRetrospective observation after 24 months after the spinal procedure

Retrospective evaluation of patients before the procedure, and prospective evaluation of patients 24 months after the spinal procedure, comparing the MRI changes and procedure impact on fatty muscle degeneration process

OTHERRetrospective observation after 12 months after the spinal procedure

Retrospective evaluation of the patient status before the procedure, and prospective evaluation of patients for 12 months after the spinal procedure, comparing the MRI changes

OTHERProspective evaluation of patients after 12 and 24 months after the spinal procedure

Prospective evaluation of patients after 12 and 24 months after the spinal procedure, comparing the MRI changes

Sponsors

R-CLINIC s.r.o.
CollaboratorOTHER
Faculty Hospital Nitra
CollaboratorOTHER
Slovak Academy of Sciences
CollaboratorOTHER_GOV
University Hospital Bratislava
CollaboratorOTHER
Europainclinics z.ú.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years

Inclusion criteria

* patient age 18-60 years * first spinal surgery in the areas L1-S1 * signed informed consent for the participation in the study

Exclusion criteria

* patients with a history of other back problems (compression fracture, spondylitis, tumour) * patients after repeated spinal surgeries * patients with a systemic disease affecting the muscles elite athletes * patients who disagree to participate in the study * women with a positive pregnancy test or women planning on becoming pregnant

Design outcomes

Primary

MeasureTime frameDescription
Fat degeneration of muscles12 months after procedureFat degeneration of musculus erector spinae and multifidus muscles evaluated by comparing the pre-operative current MRI of the lumbosacral spine using the 2-point Dixon Technique and Goutallier classification in each group
Oswestry disability index (ODI)12 months and 24 months after procedureODI is based on a questionnaire, which includes 10 items, each one has 6 possible answers. Each item is rated from 0 to 5 and the sum of all answers is evaluated on a scale from 0-100, with higher scores meaning more serious symptoms.
EQ-5D-5L12 months after procedureEQ-5D is a standardized questionnaire tool developed by the EuroQol group as a measure of the quality of life linked to health, that can be used in a wide spectrum of health conditions and their treatment. The system has 5 dimensions: mobility, being able to take care of oneself, every-day activities, pain/discomfort and anxiety/depression. Each system can be graded from 1-5, where 1 means no problems in the area and 5 meaning extreme problems. T Changes in the visual analogue scale (VAS) of lower limb pain evaluated on a scale of 0 to 10

Secondary

MeasureTime frame
Usage of painkillers before and after the procedures12 months after procedure
Occurrence of early and late post-surgery complications12 months after procedure

Countries

Slovakia

Contacts

Primary ContactLadislav Kocan, MD PhD
europainclinicsstudy@gmail.com+421557891100
Backup ContactRobert Rapcan, MD PhD FIPP
rapcan@europainclinics.com

Outcome results

None listed

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