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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03794830
Other study ID # 041218
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 4, 2018
Est. completion date January 4, 2019

Study information

Verified date February 2019
Source University of Extremadura
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary focus of this study is to know the influence of sacroiliac joint manipulation on low back pain with or without radiation to lower limbs, in the lumbopelvic-hip joint


Description:

One of the main problems faced by physiotherapists in primary care is low back pain with or without radiation to lower limbs. Nowadays, there are a lot of types of low back pain interventions, yet despite the vast amount of research findings, the evidence remains contradictory and inconclusive: Pharmacological treatments like NSAIDs have shown result in acute low back pain but not in chronic pain; conservative interventions (ultrasound, interferential currents, mechanical traction and massage) have been studied and found ineffective.

A total of 151 low back pain patients with or without radiation to lower limbs between 18-70 years old derived from the Physiotherapy Unit of GĂ©vora Health Center (Badajoz, Spain) voluntarily entered the study


Recruitment information / eligibility

Status Completed
Enrollment 151
Est. completion date January 4, 2019
Est. primary completion date January 4, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- dysfunction or sacroiliac joint hypomobility (SI)

- having stopped taking anti-inflammatory medicines or analgesics three days before the study began

Exclusion Criteria:

- destructive injuries of the spine and pelvis

- fractures

- lumbar surgery

- sacroiliac instability

- spondylolisthesis

- pregnancy in progress

- cauda equina syndrome

- abdominal aneurysm

- infection

- inflammatory arthritis

- tumors

- osteoporosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
manipulation group (MG)
Patients were treated with sacroiliac joint osteopathic semidirect manipulation twice a week every 3 to 4 days over a period of time of 3 weeks
electrotheraphy group (EG)
Patients were treated with micro-waves (circular antenna in lumbar area, pulsating-mode 120W for 12 minutes) and later conventional analgesic TENS (80Hz frequency, 30 minutes) 5 days per week over a period of time of 3 weeks (15 sessions)

Locations

Country Name City State
Spain Universidad de Extremadura Badajoz

Sponsors (1)

Lead Sponsor Collaborator
University of Extremadura

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary visual analogue scale (VAS) Pain assessment from 0 to 10. 0: no pain 10: maximum pain 1 week
Primary Oswestry disability index (ODI) disability assessment 0% -20% (Minimum Disability) 21% -40% (Moderate disability) 41% -60% (Severe disability) 61% -100% (Disabled): 1 week
Primary Roland Morris questionnaire disability assessment The extreme values oscillate between 0 (absence of disability due to low back pain) and 24 (maximum possible disability) 1 week
Primary digital algometer (Wagner, FPIX model) Pain threshold assessment by pressing the sensitive points of the muscle 1 week
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