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Back Pain clinical trials

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NCT ID: NCT03058315 Completed - Low Back Pain Clinical Trials

Disease Perception and Recovery From Low Back Pain

Start date: April 1, 2017
Phase:
Study type: Observational

The main purpose of the study is to investigate the importance of patients' beliefs regarding staying active despite low back pain, among patients referred from general practice to secondary care treatment in Denmark. It is hypothesised that patients believing that staying active will help them recover will have higher odds of a 30%-improvement in The Roland Morris Disability score after 52 weeks compared to patients disagreeing that staying active will lead to better recovery.

NCT ID: NCT03055845 Completed - Low Back Pain Clinical Trials

A Single Ascending Dose Study of Safety and Tolerability of STA363 Compared to Placebo in 15 Patients With Chronic Discogenic Low Back Pain

Start date: March 27, 2017
Phase: Phase 1
Study type: Interventional

A phase I, randomized, double-blinded, placebo-controlled, single ascending dose study to investigate the safety, local tolerability and transformation of nucleus pulposus following intradiscal injection of STA363 or placebo in patients with discogenic low back pain. 15 patients will participate in either of 3 dose groups, each comprising 5 patients: - Group 1: STA363 dose 1 (3 patients) or placebo (2 patients) - Group 2: STA363 dose 2 (3 patients) or placebo (2 patients) - Group 3: STA363 dose 3 (3 patients) or placebo (2 patients)

NCT ID: NCT03049644 Completed - Clinical trials for Chronic Lower Back Pain

A Trial Comparing Mechanical Diagnosis and Treatment to Manual Therapy

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Mechanical diagnosis and treatment (MDT) and Manual Therapy (MT) have both demonstrated efficacy in the management of CLBP. The use of a Point of Care (POC) design in this study will allow for comparison of these two treatment modalities in a clinical setting. The purpose of this study is to demonstrate the feasibility of recruiting, enrolling and collecting outcome data on CLBP patients utilizing the POC methodology.

NCT ID: NCT03047044 Completed - Back Pain Clinical Trials

The Comparison of Postoperative Pain After Lumbar Fusion Surgery in Intravenous Patient-controlled Analgesia Between Conventional Mode and Optimizing B.I Mode With 'PAINSTOP' Equipment

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

The postoperative pain of lumbar fusion surgery is very severe that it is necessary to use additional analgesics as well as a patient controlled analgesia (PCA). The most common pain control method of this surgery is the intravenous (IV) PCA. but, if it is relatively insufficient amount of narcotic analgesics ,in the case of IV PCA, may be failed to reduce the pain intensity effectively. Consequently, it may result in the a lot of rescue analgesics requirement, which leads to the adverse effects in patients who are very sensitive to narcotic analgesics. In addition, the patient's satisfaction to the PCA may be low compared with that of expected. For the recently released PCA instrument 'PAINSTOP', the investigators can specify the mode setting including total volume, flow rate (basal rate) per hour, bolus dose, and lock out time (LOT). Furthermore, this device can be set to optimize basal infusion (B.I), which is a new mode, so that the administered rate and amount of drug can be increased or decreased according to the patient's use of bolus button. Therefore, this PCA device can be implemented to the conventional mode, and added the function of automatically controlling the basal rate and administered amount of drug according to the use demand of the patient. However, since there are few studies related to this new mode of PCA, more research is needed in patients with postoperative pain.

NCT ID: NCT03040310 Completed - Low Back Pain Clinical Trials

Personalized Back Rx Exercise Program as a Treatment for Discogenic Low Back Pain

Start date: January 2016
Phase: N/A
Study type: Interventional

The prevalence and disability associated with discogenic low back pain are significant, and there is a general lack of widely accepted conservative treatments for the condition. A majority of previous studies that have assessed the efficacy of self-directed exercise-based rehabilitation programs did not include comprehensive metrics to confirm whether participants actually participated in the exercises prescribed. In this pilot study, the investigators hope to determine whether proxies of compliance with a daily, self-directed rehabilitation program for discogenic low back pain are correlated with participant-reported improvements in pain and function. The feasibility of a mobile interface designed to help patients with chronic low back pain track the daily management of their conditions will also be evaluated.

NCT ID: NCT03038529 Completed - Low Back Pain Clinical Trials

Variable Approaches of Intradiscal O3-O2 Injection

Start date: January 1, 2015
Phase: N/A
Study type: Interventional

Cost Intradiscal injection of ozone-oxygen mixture (O3-O2) which offers a rapid onset amelioration of symptoms, with a sustained duration pain relief in low back pain. Does change of injection approach make a difference?

NCT ID: NCT03031158 Completed - Low Back Pain Clinical Trials

Hip-spine Intervention for Older Adults With Chronic Low Back Pain

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Low back pain (LBP) is extremely common in older adults and is associated with a host of negative consequences, including decreased physical function and increased healthcare utilization. Among older adults with LBP, hip impairments indicative of hip joint disease are more prevalent and associated with greater disability than among older adults without LBP. This study will investigate a novel intervention designed to improve LBP-related disability by combining a typical spine-focused exercise program with a hip-focused intervention.

NCT ID: NCT03023969 Completed - Pain, Chronic Clinical Trials

Implication of Two Doses of O2-O3 Upon the Pain Alleviation in Patients With Low Back Pain

Start date: August 2015
Phase: N/A
Study type: Interventional

Low back pain is very common problem, variable modalities have been introduced to control such problem. One of the emerging modalities is the ozone - oxygen (O2-O3 ) mixture that could reduce the herniation disk size and inflammation.

NCT ID: NCT03021278 Completed - Low Back Pain Clinical Trials

Tactile Acuity in Experimentally Induced Acute Low Back Pain

Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether experimentally induced acute low back pain might lead to alteration in lumbar tactile acuity measured in region affected by pain compared to pain-free side and pain-free controls.

NCT ID: NCT03016676 Completed - Clinical trials for Chronic Non Specific Low Back Pain

Efficacy of SM on Postural Instability and Quality of Life in Patients With Chronic Non Specific Low Back Pain(CNSLBP)

Start date: July 2015
Phase: N/A
Study type: Interventional

This study will give a new insight to the physiotherapy fraternity in the effects of spinal manipulation in as clinical practice, as well as the patient's community in quick re-establishment of functional ability, pain decrease, and improvement of quality of life for economic reasons. In this high opinion, application of short-term intensive spinal manipulation for non specific chronic low back pain treatment is desirable.