Clinical Trials for Back Pain

Currently registered clinical trials for Back Pain from ClinicalTrials.gov. 14 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Back Pain from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 14
  • Active, not recruiting: 4
  • Completed: 17
  • Other: 15

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT01719055 — RELIEF - A Global Prospective Observational Post-Market Study to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain

StatusRecruiting
PhaseN/A
SponsorBoston Scientific Corporation
Enrollment4800
Study TypeOBSERVATIONAL
ConditionsPain
Interventions

To compile characteristics of real-world clinical outcomes for Boston Scientific commercially approved neurostimulation systems for pain in routine clinical practice, when used according to the applicable Instructions for Use

- and -

To evaluate the economic value and technical performance of Boston Scientific commercially approved neurostimulation systems for pain in routine clinical practice

NCT05345015 — High Frequency RF Current Effects on Muscle Pain and Function

StatusRecruiting
PhaseN/A
SponsorAristotle University Of Thessaloniki
Enrollment200
Study TypeINTERVENTIONAL
ConditionsTranscutaneous Electric Nerve Stimulation; Chronic Low-back Pain; Hamstring Injury; Muscle; Injury, Quadriceps (Thigh); Physical Therapy
Interventions;

The purpose of this study is to examine the acute and chronic effects of high frequency electrical current transfer (frequently called “TECAR”) on pain and functional movement in individuals with a musculoskeletal injury or pain. The participants will be assigned into an experimental or a control group and outcome measures will be measured prior to, after, 24 and 48 hours following a single int…

NCT07690449 — Three CT Signs of Nerve-root Suffering in Low-back Sciatica: a Study of Their Frequency in Patients Referred for CT-guided Nerve-root Infiltration.

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment400
Study TypeOBSERVATIONAL
ConditionsSciatica; Lumbosacral Radiculopathy; Low Back Pain
Interventions

Retrospective, observational, single-centre study conducted at Nice University Hospital (Pasteur 2), Department of Diagnostic and Interventional Radiology. Objective: to assess the prevalence of three CT signs sought next to the clinically suspected nerve root in patients with low-back sciatica referred for CT-guided foraminal/peri-radicular infiltration: (1) nerve-root size asymmetry/hypertrop…

NCT05037968 — MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion

StatusRecruiting
PhaseN/A
SponsorKuros Biosurgery AG
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDegenerative Disc Disease; Spine Fusion; Leg Pain and/or Back Pain
Interventions;

This is a phase IV post-marketing study for MagnetOs Flex Matrix. MagnetOs Flex Matrix is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease and undergoing spinal fusion surgery.

In this study, MagnetOs Flex Matrix will be used according to the latest U.S. Instructions For Use, specifically as a bone graft exten…

NCT06106191 — Integrative Mindfulness-Based Predictive Approach for Chronic Low Back Pain Treatment

StatusRecruiting
PhaseN/A
SponsorBoston Medical Center
Enrollment350
Study TypeINTERVENTIONAL
ConditionsChronic Low-back Pain
Interventions; ;

This study will identify unique signatures that people have which can cause pain by evaluating biological, psychological, and social markers using artificial intelligence. These markers can be used to accurately predict the response of diverse individuals with chronic low back pain (cLBP) to Mindfulness-Based Stress Reduction. This will help enhance clinician decision-making and the targeted tr…

StatusRecruiting
PhaseN/A
SponsorAnkara City Hospital Bilkent
Enrollment24
Study TypeINTERVENTIONAL
ConditionsLumbar Disc Herniation; Chronic Low Back Pain; Radicular Pain; Lumbar Radiculopathy
Interventions;

This prospective, randomized, single-blinded, controlled clinical trial aims to compare the effectiveness of high-intensity laser therapy and fluoroscopy-guided transforaminal epidural steroid injection in patients with chronic low back pain and lumbar radiculopathy. Eligible patients will be randomized into two parallel groups. One group will receive high-intensity laser therapy, and the other…

NCT07164677 — Serratus Posterior Superior Plane Block for Postoperative Pain in Cardiac Surgery

StatusRecruiting
PhaseN/A
SponsorOndokuz Mayıs University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsCardiac Surgery; Post Operative Pain, Acute
Interventions; ;

The aim of this study is to investigate the efficacy of bilateral serratus posterior superior intercostal plane (SPSIP) block on postoperative acute pain and opioid consumption in patients undergoing on-pump open-heart surgery. Postoperative outcomes including pain scores, cumulative morphine use, quality of recovery, and opioid-related side effects will be evaluated within the first 24 hours a…

NCT07190807 — Managing Pain Using Optimized Sequences by Adjusting Parameters With Independent Current Control

StatusRecruiting
PhaseN/A
SponsorBoston Scientific Corporation
Enrollment70
Study TypeINTERVENTIONAL
ConditionsChronic Pain; Intractable Pain; Low Back Pain; Chronic Low-back Pain; Chronic Leg Pain
Interventions

Study to evaluate the effectiveness of time variant pulse (TVP)-SCS in patients with chronic pain using commercially approved Boston Scientific SCS Systems per local Instructions for use (IFU).

In addition, to compile real-world clinical outcomes in subjects with chronic, intractable low back and/or leg pain.

NCT07685340 — Dry Dynamic Cupping vs Instrument-Assisted Soft Tissue Mobilization for Chronic Myofascial Low Back Pain

StatusRecruiting
PhaseN/A
SponsorIbadat International University, Islamabad
Enrollment48
Study TypeINTERVENTIONAL
ConditionsChronic Myofascial Low Back Pain
Interventions;

This study aims to compare the effects of Dry Dynamic Cupping and Instrument-Assisted Soft Tissue Mobilization (IASTM) in patients with chronic myofascial low back pain. The interventions will be evaluated for their effectiveness in reducing pain, improving functional disability, and enhancing quality of life. The findings may help identify a more effective treatment approach for managing chron…

NCT07677969 — The Relationship Between Lost Extremity Percentage and Postural Control, Neck and Low Back Pain, Daily Living Activities, and Reaction Time in Individuals With Unilateral Upper Limb Amputation

StatusRecruiting
PhaseN/A
SponsorHacettepe University
Enrollment15
Study TypeOBSERVATIONAL
ConditionsUpper Limb Amputation; Postural Control; Neck Pain; Low Back Pain; Daily Activities
Interventions

This observational study aims to examine the relationship between the percentage of limb loss and functional outcomes in individuals with unilateral upper limb amputation. Upper limb amputation can affect posture, balance control, pain levels, daily living activities, hand function, and reaction time. However, limited research has investigated how the amount of limb loss influences these outcom…

NCT07681336 — Auricular Vagus Nerve Stimulation in Patients With High Impact Chronic Low Back Pain

StatusRecruiting
PhaseN/A
SponsorAlgemeen Ziekenhuis Maria Middelares
Enrollment44
Study TypeINTERVENTIONAL
ConditionsChronic Low Back Pain
Interventions;

The goal of this clinical trial is to evaluate whether auricular vagus nerve stimulation using the VIVO® device can improve function and reduce pain in adults with high-impact chronic low back pain when added to standard medical care. It will also assess the safety and usability of this therapy.

The study includes adult patients aged 30 to 55 years who have had moderate to severe chronic low b…

NCT07675304 — Evaluation of the Effectiveness and Safety of Mesotherapy in the Treatment of Chronic Low Back Pain Syndrome

StatusRecruiting
PhaseEarly Phase 1
SponsorNational Institute of Geriatrics, Rheumatology and Rehabilitation, Poland
Enrollment90
Study TypeINTERVENTIONAL
ConditionsChronic Low Back Pain (Non-specific, Uncomplicated)
Interventions;

The aim of this study is to evaluate the effectiveness of collagen mesotherapy in the treatment of chronic low back pain (CLBP) in the lumbosacral spine.

Mesotherapy is expected to reduce pain in the lumbosacral region, decrease soft tissue tension (including muscles, fascia, and ligaments), improve spinal mobility, and support subsequent physiotherapy.

A total of five treatment sessions will…

NCT07668648 — Interscalene Brachial Plexus Block Versus Serratus Posterior Superior Intercostal Plane Block for Arthroscopic Shoulder Surgery

StatusRecruiting
PhaseN/A
SponsorFerit Yetik
Enrollment80
Study TypeINTERVENTIONAL
ConditionsPostoperative Pain; Shoulder Arthroscopy
Interventions; ;

Arthroscopic shoulder surgery is associated with moderate to severe postoperative pain that may delay recovery and rehabilitation. Interscalene brachial plexus block (ISB) is widely used for postoperative analgesia in shoulder surgery; however, it may be associated with complications such as phrenic nerve paralysis. The serratus posterior superior intercostal plane (SPSIP) block is a recently d…

NCT07674407 — Fear-Avoidance Beliefs and Physical Function in Patients With Lumbar Disc Herniation

StatusRecruiting
PhaseN/A
SponsorIstinye University
Enrollment65
Study TypeOBSERVATIONAL
ConditionsDisc Herniation

Lumbar disc herniation is one of the most common causes of low back pain and is associated with substantial functional limitations and reduced quality of life, particularly among working-age individuals. Displacement of disc material toward the spinal canal may result in mechanical compression and inflammation of the nerve roots, leading to pain, restricted movement, and reduced functional perf…

Active, Not Recruiting

NCT06897280 — Clinical Trial of MED HF10™ Spinal Cord Stimulation for the Treatment of Chronic Pain

StatusActive, not recruiting
PhasePhase 4
SponsorNevro Corp
Enrollment25
Study TypeINTERVENTIONAL
ConditionsChronic, Intractable Back Pain and/or Leg Pain
Interventions

This is a single-center, prospective, non-randomized exploratory study in subjects with chronic, intractable back pain and/or leg pain per the center’s routine practice. The primary endpoint is the distribution of responders by ’lowest preferred pulse dose (PD)’ setting, where a subject is a responder to the lowest PD setting they preferred prior to entering the Observational period. The study …

NCT06104605 — Improving Access to Chiropractic Care in Community Health Centers

StatusActive, not recruiting
PhaseN/A
SponsorBoston Medical Center
Enrollment3
Study TypeINTERVENTIONAL
ConditionsLower Back Pain
Interventions; ;

The goal of this study is to evaluate the feasibility of new implementation strategies designed to increase the number of Primary Care Providers (PCPs) referrals to chiropractic care for lower back pain (LBP) in underserved populations. The investigators plan to pilot the strategies in three qualified community health centers (CHCs) and compare the number of LBP patients who receive referrals b…

NCT06001853 — Allogeneic BM-MSCs in Patients With Painful Lumbar Facet Arthropathy

StatusActive, not recruiting
PhasePhase 2
SponsorMayo Clinic
Enrollment40
Study TypeINTERVENTIONAL
ConditionsFacet-Mediated Low Back Pain; Lumbar Facet Joint Osteoarthritis
Interventions;

The purpose of this research study is to evaluate the safety and effect of bone marrow-derived stem cells for the treatment of low back pain.

NCT07050290 — Restoring Segmental Lumbar Lordosis After Failed Previous Fusion at the Same Level

StatusActive, not recruiting
PhaseN/A
SponsorN.N. Priorov National Medical Research Center of Traumatology and Orthopedics
Enrollment20
Study TypeINTERVENTIONAL
ConditionsFailed Back Surgery Syndrome; Degeneration Lumbar Spine; Degenerative Spondylolisthesis; Sagittal Imbalance
Interventions

The restoration of lumbar lordosis is mandatory during lumbar fusion surgery for degenerative disc disease, since not restoring lumbar lordosis adequately may adversely affect surgical outcomes and the patient’s quality of life in the follow-up. Revision surgery to restore segmental lordosis at the level of previous spinal fusion is extremely difficult to do and its performance is usually infer…

Not Yet Recruiting

NCT07667062 — Effects of Thoracolumbar Fascia Myofascial Release in Chronic Low Back Pain

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Health Sciences Lahore
Enrollment65
Study TypeINTERVENTIONAL
ConditionsChronic Non-specific Low Back Pain
Interventions;

The thoracolumbar fascia (TLF) is thickened and stiffer in individuals with chronic non-specific low back pain (CNSLBP) and may contribute to pain persistence. Myofascial release (MFR) has been shown to reduce TLF stiffness acutely; however, its longer-term effects on fascial morphology and pain self-efficacy remain unclear. This randomized controlled trial will investigate the effects of a sta…

NCT07672197 — Psoas Major Muscle Intervention on Chronic Lumbar Pain in Cleaning Professionals.

StatusNot yet recruiting
PhaseN/A
SponsorEscola Superior de Tecnologia da Saúde do Porto
Enrollment30
Study TypeINTERVENTIONAL
ConditionsLumbar Pain; Non-specific Low Back Pain (NSLBP)
Interventions;

The goal of this randomized controlled trial is to determine the effect of a psoas major muscle intervention on non-specific and chronic lumbar pain in cleaning professionals. It is expected that this intervention will reduce the severity and frequency of symptoms. This study aims to evaluate the effect of psoas major stretching techniques. To collect data, participants will rate their pain int…

NCT07674836 — SPSIP Block Versus ESP Block for Chronic Pain After Unilateral Breast Surgery

StatusNot yet recruiting
PhaseN/A
SponsorEngin Çetin
Enrollment90
Study TypeINTERVENTIONAL
ConditionsPostoperative Pain; Opioid Use
Interventions;

This prospective, randomized, assessor-blinded study will compare serratus posterior superior intercostal plane block and erector spinae plane block in adult female patients undergoing unilateral breast surgery. The primary outcome is chronic postoperative pain at 3 months, assessed using the Brief Pain Inventory-Short Form.

NCT07677189 — Sensorimotor Balance Training for Chronic Nonspecific Low Back Pain

StatusNot yet recruiting
PhaseN/A
SponsorNajran University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsChronic Nonspecific Low Back Pain
Interventions;

Chronic nonspecific low back pain is one of the most common causes of pain and disability worldwide. Many people with chronic low back pain experience difficulties with balance, posture, movement control, and daily activities. Sensorimotor balance training is a rehabilitation approach designed to improve balance, body awareness, and neuromuscular control.

The purpose of this randomized control…

NCT07668466 — Intradiscal rhGDF-6 for the Treatment of Lumbar Disc Degeneration

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorCartago Biotech Pty Ltd
Enrollment60
Study TypeINTERVENTIONAL
ConditionsDisc Degenerative Disease; Back Pain
Interventions;

The goal of this clinical trial is to find out if a new medicine can help people who have long-lasting back pain caused by damaged spinal discs. The study will also check if the medicine is safe to use.

The main questions this study aims to answer are:

Is the medicine safe, and what amount works best? Can it reduce long-term back pain?

Researchers will test a medicine called CBT005, which co…

NCT07688564 — Exercise Interventions for Overweight Men With Chronic Low Back Pain

StatusNot yet recruiting
PhaseN/A
SponsorUniversiti Sains Malaysia
Enrollment156
Study TypeINTERVENTIONAL
ConditionsNon-specific Chronic Low Back Pain; Central Sensitization
Interventions; ;

This randomized controlled trial aims to compare the effectiveness of motor control exercise, aerobic walking exercise, and muscle strengthening exercise in overweight male adults with non-specific chronic low back pain and central sensitization. A total of 156 participants will be randomly assigned to one of four groups: motor control exercise plus patient education, aerobic walking exercise p…

NCT07683676 — Kinetic Control Training Versus Core Stability Exercises on Proprioception and Spatiotemporal Gait Parameters in Chronic Non-specific Low Back Pain

StatusNot yet recruiting
PhaseN/A
SponsorCairo University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsLow Back Pain
Interventions; ;

This study will be conducted to comapre between kinetic control training versus core stability exercises on proprioception and spatiotemporal gait parameters in chronic non-specific low back pain.

NCT07670533 — The Lumbar Adjacent Segment Stenosis Trial

StatusNot yet recruiting
PhaseN/A
SponsorOslo University Hospital
Enrollment192
Study TypeINTERVENTIONAL
ConditionsLumbar Adjacent Spinal Stenosis; Chronic Low Back and Leg Pain
Interventions;

The goal of this clinical trial is to learn if there are differences in the effectiveness of decompression surgery alone versus decompression combined with extended fusion in patients with a previous lumbar spinal fusion who now present with symptoms of lumbar adjacent segment stenosis (LASS). The main questions it aims to answer are:

  • Does decompression alone differ from decompression combin…

NCT07670078 — Comparıson of Analgesıc Effıcacy of Dıfferent Volumes of Serratus Posterior Superıor Intercostal Plane Block After Modıfıed Radıcal Mastectomy Surgery

StatusNot yet recruiting
PhaseN/A
SponsorCumhuriyet University
Enrollment90
Study TypeINTERVENTIONAL
ConditionsModified Radical Mastectomy; Post Operative Pain, Acute; Facial Plane Blocks
Interventions; ;

The aim of researchers is to compare the effects of three different local anesthetic concentrations and volumes on opioid consumption, postoperative analgesic efficacy, and pain scores during ultrasound-guided SPSIP blocks in patients undergoing modified radical mastectomy. Additionally, we aim to map and identify the dermatomal areas where different concentrations and volumes of SPSIP blocks p…

NCT07679178 — Comparing Strategies to Improve Non-Pharmacologic Pain Relief for Adults With Back Pain Using the Education, Navigated Care, and Supported Self-management Pain Care Program

StatusNot yet recruiting
PhaseN/A
SponsorDuke University
Enrollment530
Study TypeINTERVENTIONAL
ConditionsChronic Low-back Pain (cLBP); High-Impact Chronic Pain (HICP)
Interventions

The goal of this clinical trial is to help Veterans manage high-impact chronic low back pain. The trial will use a program, ENCompaSS (Education, Navigated Care, and Supported Self-Management) designed to reduce pain more than usual care alone. Researchers will assess a) the impact of ENCompaSS, b) identify which Veterans benefit the most, and c) how this program can be delivered more broadly i…

NCT07566312 — Study of QL Analgesic Response and Extent

StatusNot yet recruiting
PhasePhase 4
SponsorDuke University
Enrollment25
Study TypeINTERVENTIONAL
ConditionsAcute Pain; Postoperative Pain; Regional Anesthesia Block
Interventions

A total of 14-18 healthy volunteers will be included. There will be three different procedure days, separated by at least one week. On each visit, the subjects will receive a QL block, according to the randomization process. Each volunteer will undergo pre-procedure screening on the first visit. The blocks will be performed on the same side, by the same anesthesiologist, with at least one week …

Enrolling by Invitation

NCT07684118 — Egoscue and Core Stabilization for Chronic Low Back Pain

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Lahore
Enrollment64
Study TypeINTERVENTIONAL
ConditionsChronic Low Back Pain (CLBP)
Interventions;

Chronic low back pain is a widespread musculoskeletal condition that limits mobility and affects quality of life. It is often caused due to the poor posture, hyperlordosis and weak core muscles. This randomized clinical trial aims to evaluate the effectiveness of egoscue based postural correction combined with core stabilization exercises compared to core stabilization exercises alone in managi…

NCT07683273 — Diaphragmatic Breathing Exercises and Chronic Non-spesifik Neck and Back Pain

StatusEnrolling by invitation
PhaseN/A
SponsorHacettepe University
Enrollment42
Study TypeINTERVENTIONAL
ConditionsNeck Pain Musculoskeletal; Back Pain
Interventions;

Effects of Diaphragmatic Breathing Exercises Added to Posture and Core Stabilization Training on Pain, Body Awareness and Cardiovascular Parameters in Women with Chronic Non-spesific Neck and Back Pain

Completed Trials

NCT01293019 — Osteopathic Treatment in Adult Patients With Cystic Fibrosis

StatusCompleted
PhasePhase 3
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment32
Study TypeINTERVENTIONAL
ConditionsCystic Fibrosis; Back Pain; Neck Pain; Chest Pain
Interventions; ;

To study the contribution of osteopathy on the reduction of pain in adult patients with cystic fibrosis

NCT03680846 — Comparison of HF10 Therapy Combined With CMM to CMM Alone in the Treatment of Non-Surgical Refractory Back Pain

StatusCompleted
PhaseN/A
SponsorNevro Corp
Enrollment211
Study TypeINTERVENTIONAL
ConditionsBack Pain
Interventions;

This study is being conducted to document the safety, clinical effectiveness and cost-effectiveness of high-frequency SCS at 10 kHz (HF10™ Therapy) delivered through the Senza system in subjects with chronic refractory back pain (with or without leg pain) who are not considered candidates for spine surgery. This study is a multi-center, prospective, randomized study to compare the two treatment…

NCT02555280 — Coflex PS3 Actual Conditions for Use Study

StatusCompleted
PhaseN/A
SponsorCompanion Spine, LLC
Enrollment40
Study TypeINTERVENTIONAL
ConditionsSpinal Stenosis Lumbar
Interventions;

A 2 and 5 year evaluation of clinical outcomes in the treatment of degenerative spinal stenosis with concomitant low back pain by decompression with additional stabilization using the coflex® Interlaminar Technology for FDA Actual Conditions of Use Study.

NCT07686237 — Core Stability Training in Young Adults With Chronic Non-Specific Low Back Pain

StatusCompleted
PhaseN/A
SponsorGuangxi Normal University
Enrollment30
Study TypeINTERVENTIONAL
ConditionsChronic Non-specific Low Back Pain
Interventions;

Chronic non-specific low back pain is common among young adults and can lead to persistent pain, reduced physical function, decreased muscle strength, and impaired balance, affecting daily activities and quality of life. Core stability exercises are widely used in rehabilitation programs for low back pain, but the effectiveness of Swiss ball-based core stability training in young adults with ch…

NCT05096494 — Safety and Efficacy of SP-103 in Subjects With Moderate to Severe Acute Lower Back Pain

StatusCompleted
PhasePhase 2
SponsorScilex Pharmaceuticals, Inc.
Enrollment76
Study TypeINTERVENTIONAL
ConditionsModerate to Severe Acute Lower Back Pain
Interventions;

This is a Phase 2, randomized, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the safety and efficacy of SP-103 in subjects with moderate to severe acute lower back pain.

NCT06412484 — State vs. Trait Alterations in Low Back Pain

StatusCompleted
PhaseN/A
SponsorSchweinhardt Petra
Enrollment105
Study TypeOBSERVATIONAL
ConditionsLow Back Pain
Interventions; ;

The primary goal of this study is to investigate whether different alterations observed in patients with non-specific episodic low back pain (compared to healthy volunteers), detected using several assessments: psychophysical and neurophysiological testing, imaging, and blood sampling, are dependent or independent of the presence and type of pain experienced at the time of investigation.

NCT06272539 — Spinal Cord Stimulation Combined With Exercise in Persistent Spinal Pain Syndrome

StatusCompleted
PhaseN/A
SponsorFundación Universidad Católica de Valencia San Vicente Mártir
Enrollment36
Study TypeINTERVENTIONAL
ConditionsFailed Back Surgery Syndrome
Interventions;

Introduction. At the neurophysiological level, it is possible to observe an increase in the central processing of pain in patients diagnosed with persistent Spinal Pain Syndrome (PSPS-T1/2), potentially stemming from dysfunctions in the endogenous facilitation and inhibition of pain. Administration of high doses of spinal cord stimulation to individuals with PSPS-T1/2 may induce supraspinal des…

NCT06660875 — Comparison of Postoperative Analgesic Efficacy of SPSIPB and Combination of IBPB and SCPB

StatusCompleted
PhaseN/A
SponsorAnkara Etlik City Hospital
Enrollment80
Study TypeINTERVENTIONAL
ConditionsShoulder Arthroscopy; İnterscalene Brachial Plexus Block; Superficial Cervical Plexus Block; Serratus Posterior Superior Intercostal Plane Block
Interventions;

Shoulder arthroscopy is one of the frequently performed surgical procedures today. After shoulder surgery, ensuring sufficent analgesia is necessary for both the patient’s comfort and for the early and regular performance of the required postoperative rehabilitation exercises. Nerve blocks provide better pain control, opioid consumption in the postoperative period, and consequently have advanta…

NCT07287761 — Comparison of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block in Postoperative Pain Management After Coronary Artery Bypass Grafting

StatusCompleted
PhaseN/A
SponsorAnkara Education and Research Hospital
Enrollment55
Study TypeOBSERVATIONAL
ConditionsPostoperative Pain After Thoracic Surgery; Coronary Artery Bypass Graft (CABG)

Coronary Artery Bypass Grafting (CABG) is a common surgical procedure for ischemic heart disease, but it often leads to severe acute and chronic postoperative pain, which can delay recovery and reduce patient comfort. Effective pain management is crucial to prevent pulmonary complications and long hospital stays. Peripheral nerve blocks are increasingly used to reduce opioid consumption and imp…

NCT07671196 — Validity and Reliability of Arabic Version of Extended Aberdeen Spine Pain Scale

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment300
Study TypeOBSERVATIONAL
ConditionsNonspecific Spinal Pain (Including Cervical, Thoracic, and Lumbar Spinal Pain)

The goal of this observational study is to determine whether the Arabic version of the Extended Aberdeen Spine Pain Scale (EASPS) is a valid and reliable tool for assessing spine-related pain and functional disability in Arabic-speaking adults with nonspecific spinal pain.

The main questions it aims to answer are:

  • Is the Arabic version of the EASPS a valid instrument for evaluating spine-re…

NCT07171125 — Liposomal Bupivacaine for Pain After Lumbar Fusion

StatusCompleted
PhasePhase 4
SponsorMin Li
Enrollment204
Study TypeINTERVENTIONAL
ConditionsPostoperative Acute Pain; Lumbar Degenerative Diseases
Interventions;

Spine surgery often causes severe postoperative pain. Currently, our hospital routinely uses ropivacaine for local infiltration analgesia (lasting 6-8 hours). This study evaluates liposomal bupivacaine, a novel long-acting local anesthetic providing up to 72 hours of pain relief, in patients undergoing posterior lumbar spine surgery. Through a randomized controlled design, we will compare the t…

NCT07680231 — Smartphone Versus Back Range of Motion: Validity and Reliability in Lumbar Range of Motion Assessment

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment120
Study TypeOBSERVATIONAL
ConditionsLumbar Pain Syndrome
Interventions;

This study aims to investigate the clinimetric properties of the iPhone Level application as a suitable alternative to the Back Range of Motion device in assessing lumbar range of motion, including flexion, extension, and lateral flexion.

NCT07292350 — Investigation of the Effects of a Neuromuscular Control-Focused Posture Training Program in Butchers

StatusCompleted
PhaseN/A
SponsorUskudar University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsWork-related Illness; Neck Pain; Back Pain
Interventions;

The aim of this study was to evaluate the effect of a neuromuscular posture training program implemented in butchers on neck pain, posture quality and upper back muscle control.

NCT07327827 — Comparative Effects of Back School Based Intervention Versus Cranio-Cervical Muscle Training in Computer Users With Cervicogenic Headache

StatusCompleted
PhaseN/A
SponsorLahore University of Biological and Applied Sciences
Enrollment44
Study TypeINTERVENTIONAL
ConditionsCervicogenic Headache
Interventions;

The aim of the study is to compare Back School Based Intervention with Cranio- Cervical muscle training in participants with Cervicogenic headache. The study wants to investigate that which intervention helps to mange pain, improve posture and reduce disability. The study aims to answer the question:

  • How effective is Back School Based intervention on pain, posture and disability in computer …

NCT07337187 — Effect of Thread-Embedding Acupuncture at EX-B2 Acupoint on Pain Intensity and Quality of Life in Chronic Low Back Pain

StatusCompleted
PhaseN/A
SponsorIndonesia University
Enrollment32
Study TypeINTERVENTIONAL
ConditionsLow Back Pain
Interventions;

The goal of this clinical trial is to learn whether thread-embedding acupuncture (TEA) is more effective than sham thread-embedding acupuncture in treating adults with chronic low back pain. The study will also evaluate the safety of TEA.

The main questions it aims to answer are:

  • Does TEA reduce pain intensity more effectively than sham TEA?
  • Does TEA improve quality of life compared with …

NCT07543952 — Reformer Pilates vs Conventional Physiotherapy in Chronic Low Back Pain

StatusCompleted
PhaseN/A
SponsorUskudar University
Enrollment42
Study TypeINTERVENTIONAL
ConditionsLow Back Pain
Interventions;

Non-specific chronic low back pain is one of the most prevalent musculoskeletal disorders worldwide and is associated with functional limitations and reduced quality of life. Exercise-based physiotherapy approaches are strongly recommended in clinical guidelines. Pilates exercises are frequently used due to their potential effects on core stability and movement control, while conventional physi…

NCT07395102 — Effectiveness of Thread-Embedding Acupuncture at EX-B2 on the Oswestry Disability Index and Finger-to-Floor Distance in Chronic Low Back Pain

StatusCompleted
PhaseN/A
SponsorIndonesia University
Enrollment32
Study TypeINTERVENTIONAL
ConditionsChronic Low-back Pain
Interventions;

Chronic low back pain (CLBP) is a leading cause of disability worldwide and significantly impairs functional capacity and quality of life. Non-pharmacological therapies are recommended as first-line management, and acupuncture has demonstrated potential benefits in reducing pain and disability. Thread embedding acupuncture (TEA) is a modified acupuncture technique that provides prolonged stimul…

Other (Terminated)

NCT02192398 — Effect of Guanfacine on the Reversal of Opioid-induced Hyperalgesia (OIH)

StatusTerminated
PhaseN/A
SponsorMassachusetts General Hospital
Enrollment8
Study TypeINTERVENTIONAL
ConditionsChronic Pain
Interventions;

Combination of guanfacine with opioid medication as a standard treatment for chronic pain.

NCT05409443 — Conventional vs Bipolar SIJ RFA for Treatment of Sacroiliac Joint Pain

StatusTerminated
PhasePhase 4
SponsorUniversity of Utah
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSacroiliac Joint Complex; Low Back Pain
Interventions;

Specific Aims The sacroiliac joint complex (SIJC) is a diathrodial, synovial joint and posterior ligamentous network that receives both anterior innervation from the lumbosacral plexus as well as posterior sensory innervation via the posterior sacral network (PSN). The PSN is comprised by the lateral branches S1-S3 posterior rami, with variable contributions from S4 lateral branch, L4 medial br…