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Clinical Trials/NCT02699164
NCT02699164
Completed
Not Applicable

Lumbal Disk Herniasyonunda farklı Tedavi yöntemlerinin etkinliğinin karşılaştırılması

Hacettepe University0 sites20 target enrollmentJanuary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lumbar Disc Herniation
Sponsor
Hacettepe University
Enrollment
20
Primary Endpoint
herniation thickness
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study was conducted with the aim of determining whether or not Non surgical spinal decompression therapy was effective in remission of herniation, decreasing pain and improving functional status.

Detailed Description

Both groups received combination of electrotherapy, deep friction massage and stabilization exercise for fifteen session. Combine group received non surgical spinal decompression therapy (NSDT) different from conventional physiotherapy group. Numeric Analog Scale, Straight leg raise (SLR) test, Oswestry Disability Index (ODI) were applied at baseline and after treatment. Disc height and herniation thickness were measured on Magnetic Resonance Imagination (MRI) which performed at baseline and three months after therapy.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
June 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Aynur Demirel

Research asisstant

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • diagnosed as lumbar disc herniation suffering from low back pain at least 8 weeks

Exclusion Criteria

  • undergone any spinal surgery clinical diagnosis of osteoporosis clinical diagnosis of scoliosis and spondylolisthesis any neurological disease causes sensorial loss

Outcomes

Primary Outcomes

herniation thickness

Time Frame: change from baseline in herniation thickness and disc height at three months

herniation thickness were measured on MRI.

Secondary Outcomes

  • function(up to 3 months)
  • mobility(up to 3 months)
  • pain severity(change form baseline in pain severity at 15 sessions of treatment)

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