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Low Back Pain clinical trials

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NCT ID: NCT05843149 Terminated - Clinical trials for Chronic Low-back Pain

Manual Therapy/Exercises vs. Physiotherapy/Back School vs. Waiting List in Patients With Chronic Low Back Pain

Start date: May 2, 2023
Phase: N/A
Study type: Interventional

A randomized controlled trial for patients with chronic low back pain with two treatment arms and one waiting list control group. Primary outcome is pain intensity on VAS.

NCT ID: NCT05213845 Terminated - Low Back Pain Clinical Trials

Spine Rehabilitation Using Spine Flexion / Extension Full Active Range of Motion for Patients With Chronic Low Back Pain

REACTIVE
Start date: February 17, 2022
Phase: N/A
Study type: Interventional

The main objective of this study is to assess efficacy of a spine rehabilitation program, using spine flexion and extension full active range of motion, on physical disability of patients with chronic low back pain.

NCT ID: NCT04990518 Terminated - Clinical trials for Low Back Pain, Mechanical

Physical Deconditioning in COVID-19 Positive Patients and Non-Specific Low Back Pain

Phydel
Start date: November 5, 2022
Phase:
Study type: Observational

The purpose of this study is to take advantage of cohorts of patients followed for Coronavirus Disease 2019 (COVID19) expected to present poor physical fitness as the consequence of COVID19 to explore the relationship between physical fitness and low back pain (LBP). Level of physical fitness will be measured at baseline and incidence and intensity of LBP will be recoreded over 1 year.

NCT ID: NCT04783532 Terminated - Pain Clinical Trials

Feasibility of Telehealth Mindfulness for Back Pain in the Emergency Department

Start date: March 5, 2021
Phase: N/A
Study type: Interventional

While guideline-directed nonpharmacological strategies for chronic low back pain are well established, optimal chronic pain management for emergency department patients has yet to be defined. Mindfulness interventions can be used for management of chronic conditions, yet are understudied as a primary approach for patients with chronic pain discharged from the emergency department. Currently, there is limited evidence examining whether an individual telehealth mindfulness intervention is a feasible and acceptable for these patients. This study will develop, pilot, and evaluate the feasibility and effects of an 8-session (12-week) telehealth mindfulness intervention for patients with an acute exacerbation of chronic low back pain

NCT ID: NCT04739839 Terminated - Low Back Pain Clinical Trials

Risk Factors for Low Back Pain in Adults A 23-year Prospective Cohort Study of 14-15-year-old Schoolchildren.

Start date: February 5, 2021
Phase:
Study type: Observational

The incidence of low back pain (LBP) is increasing and prognostic factors for developing LBP are unclear. Based on questionnaires, different prognostic factors are being explored over time.

NCT ID: NCT04585386 Terminated - Lumbar Disc Disease Clinical Trials

Efficacy of the ATLAS Medical Device on Pain in Patients With Low Back Pain Due to Lumbar Disc Disease

AmbuTract
Start date: August 18, 2021
Phase: N/A
Study type: Interventional

Monocentric, comparative, randomized, controlled interventionnal study in 2 parallel groups, aiming to compare the efficacy of the ATLAS device with that of a standard lumbar belt on the reduction of pain felt in patients with subacute or chronic low back pain with lumbar disc disease.

NCT ID: NCT04544709 Terminated - Chronic Pain Clinical Trials

Intradiscal Platelet Rich Plasma

Start date: February 14, 2019
Phase: Phase 4
Study type: Interventional

To assess changes in pain and function in patients with discogenic low back pain after a standard of care intradiscal injection of Platelet-Rich Plasma (PRP).

NCT ID: NCT04485182 Terminated - Low Back Pain Clinical Trials

Underwater Jet Massage Therapy for Chronic Low Back Pain

Start date: June 1, 2019
Phase:
Study type: Observational

Underwater massage is the more modern variety of massages otherwise known as tangentor, where the temperature of the water of the treatment tub and the mechanical effect of the water jet is utilised. It is typical of chronic low back pain that, after the first painful episode, is repeated at 44-78% of patients. Our goals are the followings: 1. Is the beneficial effect of a Underwater massage therapy addition to a complex physiotherapy comparable to a control group with respect to clinical parameters? 2. How much does the quality of life change in an initial state and how much is it in comparison with the control group?

NCT ID: NCT04449835 Terminated - Low Back Pain Clinical Trials

The Intracept Global Registry ( TIGR ) - Pilot Study

Start date: July 31, 2020
Phase:
Study type: Observational [Patient Registry]

The Intracept Global Registry is a prospective, noninterventional, observational global post market independent data collection of the ongoing effectiveness, safety, and satisfaction outcomes for patients treated with the Intracept Procedure. This registry will be conducted according to Good Clinical Practice (GCP) guidelines, including participant verbal informed consent and Independent Review Board (IRB) / Ethics Committee (EC) approval and oversight. Registry design, conduct, analysis, and reporting are overseen by the Principal Investigator (PI) and the cross-specialty TIGR Physician Steering Committee.

NCT ID: NCT04240483 Terminated - Low Back Pain Clinical Trials

Intracutaneous Sterile Water Injections for Acute Low Back Pain in the Emergency Department

Start date: July 27, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of intracutaneous sterile water injections (ISWI) for treatment of acute low back pain in patients presenting to the emergency department. The primary aim is to determine if ISWI provides pain relief for acute low back pain in the ED. The secondary aim is to evaluate whether ISWI provides improved patient satisfaction in the ED setting. The hypothesis is that ISWI will improve pain amongst patients presenting with acute low back pain to the ED.