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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03663842
Other study ID # 25/2010
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 10, 2010
Est. completion date December 10, 2010

Study information

Verified date September 2018
Source Centro Universitário Augusto Motta
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives: To analyse the effects of sciatic neural mobilisation, in combination to the treatment of the surrounding structures, on pain and disability. Secondly, to investigate baseline characteristics that may be associated with improvements in pain and lumbar disability. Methods: Twenty-eight patients with a clinical diagnosis of sciatica were treated with neural mobilization, joint mobilisation and soft tissue techniques. Pain intensity and lumbar disability were assessed at baseline and after treatment using a Numerical Rating Scale (0-10) and the Oswestry Disability Index (0-100), respectively. The pre- and post-intervention data were compared.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 10, 2010
Est. primary completion date November 10, 2010
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Low back pain with radiating leg pain and/or paresthesia below the knee that follows the L5 and/or S1 dermatomal pattern.

Exclusion Criteria:

- History of lumbar and abdominal surgery

- Rheumatologic syndromes (e.g. Rheumatoid arthritis);

- Lumbar stenosis.

Study Design


Intervention

Other:
Physical therapy treatment
All patients underwent the same techniques, and there was no modification of the intervention protocol during the study: (1) Myofascial release technique - piriformis muscle and biceps femoral muscle; (2) Hip joint mobilization; (3) Cross-fiber friction over the sacroiliac joints; (4) Neural mobilization to improve sciatic nerve excursion.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centro Universitário Augusto Motta

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity Measured by the Numerical Rating Scale (NRS 0-10) From enrollment to end of treatment at 12 weeks
Primary Lumbar disability Assessed by the Oswestry Disability Index (ODI).It consists of 10 items addressing different aspects of disability. Each item is scored from 0 to 5, with higher values representing greater disability. The sum of the item scores is divided by the total possible score (50 if all sections are completed), and the resulting total is multiplied by 100 to be described as a percentage score. From enrollment to end of treatment at 12 weeks.
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