Clinical trials: Clinic, Pain
Quadriplegia/Tetraplegia
Development and Validation of a New Questionnaire for Caregivers to Assess Hip Pain in Quadriplegic Pediatric Patients: Non-Ambulatory Hip Pain Questionnaire
The goal of this clinical trial is twofold: 1. to develop a questionnaire for care givers to assess hip pain in quadriplegic pediatric patients who are not able to communicate it independently 2.
- Trial name
- NAHPq (NCT06798233)
- Testing
- Non-Ambulatory Hip Pain questionnaire
- Where
- 2 sites in Italy
- Volunteers
- 100 people
- Sponsor
- Azienda USL Reggio Emilia - IRCCS
Amputation, Phantom Limb
Naval Medical Center San Diego (NMCSD) - Ambulatory Continuous Peripheral Nerve Blocks for Treatment of Post-Amputation Phantom Limb and Stump Pain
The purpose of this research study is to determine if putting local anesthetic-or numbing medication-through one or two tiny tube(s) placed next to the nerves that go to an amputated limb will decrease phantom limb and/or stump…
- Conditions
- Amputation, Phantom Limb, Stump Pain
- Trial name
- NCT00768248
- Testing
- perineural ropivacaine
- Where
- United States
- Volunteers
- 2 people
- Sponsor
- University of California, San Diego
Knee Osteoarthritis
"Effectiveness of Mulligan Mobilization Technique and Proprioceptive Exercises Among Patients With Knee Osteoarthritis"
This research analyzes the effectiveness of Mulligan mobilization in comparison to proprioceptive exercises for treating patients with mild to moderate Knee osteoarthritis whose condition falls under Kellgren and Lawrence grading…
- Trial name
- MWMPETKOA (NCT06971016)
- Testing
- Mulligan Mobilization technique, Proprioceptive Exercises, Traditional Physical therapy
- Where
- Pakistan
- Volunteers
- 60 people
- Sponsor
- National Healthcare Center
Pain
Comparison of Tramadol Orally Versus an Optimized Dose of Intravenous Tramadol for Postoperative Pain Relief in Ambulatory Surgery
The purpose of this study is to compare the administration of 1 unit dose of 50 mg tramadol perorally given in 3 unit dosages versus tramadol IV given in 3 unit dosage of 35 mg during the first 6 hours postoperatively and to…
- Trial name
- NCT00735748
- Testing
- Tramadol per os (Tradonal Odis® orodispersible tablets), Tramadol IV (Tradonal® IV)
- Where
- Belgium
- Volunteers
- 195 people
- Sponsor
- University Hospital, Ghent
Hand Surgery, Wrist Surgery
Early Rehabilitation After Hand or Wrist Ambulatory Surgery : How to Preserve Locomotion at Home Without Rebound Pain?
The purpose of this retrospective study is to compare the analgesic efficacy of Walant " Wide Awake Local Anesthesia No Tourniquet " with lidocaine and bupivacaine versus axillary brachial plexus block using mepivacaïne, both…
- Trial name
- WalantBAX (NCT04306666)
- Testing
- Regional anesthesia
- Where
- France
- Volunteers
- 60 people
- Sponsor
- University Hospital, Montpellier
Chronic Pain
The Application of Performance Improvement Principles to the Patient Throughput Process in an Adult Outpatient Pain Treatment Clinic
This study is undertaken to assess and improve the existing patient flow, or so-called throughput process, in an adult outpatient pain treatment clinic.
- Trial name
- NCT00888420
- Testing
- Performance Improvement Measures
- Where
- United States
- Volunteers
- 1,221 people
- Sponsor
- University of Alabama at Birmingham
Pain
Prospective, Randomized, Double Blind Study Comparing IV vs PO Acetaminophen in Patients Undergoing Lumbar Discectomy
Both intravenous and oral acetaminophen have been shown to reduce post-operative pain scores when given preoperatively. This study investigates if there is a difference between the intravenous and the oral forms when given…
- Trial name
- NCT02067442
- Testing
- oral acetaminophen, intravenous acetaminophen
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Thomas Jefferson University
Pain Management, Injection Pain Prevention
Testing the Timing and Application of Virtual Reality Distraction During Knee Injections in a VA Pain Clinic
The goal of this clinical trial is to learn whether virtual reality (VR) can be added to routine knee injection appointments at a VA outpatient pain clinic without slowing down or disrupting clinic operations.
- Conditions
- Pain Management, Injection Pain Prevention, Virtual Reality, Feasibility Studies
- Trial name
- NCT07884851
- Testing
- Immersive Virtual Reality
- Volunteers
- 45 people
- Sponsor
- Atlanta VA Medical Center
Geriatric Pain
Frailty and Chronic Pain Profiles in Patients Aged ≥65 Years
The primary aim of this study is to investigate the relationship between frailty status and pain type, pain localization, and the Geriatric Nutritional Risk Index (GNRI) in individuals aged 65 years and older who present to an…
- Trial name
- F&P (NCT07373860)
- Where
- Turkey (Türkiye)
- Volunteers
- 393 people
- Sponsor
- Ankara City Hospital Bilkent
Chronic Low Back Pain, Older Adults
Safety of Acupuncture Treatments for Chronic Low Back Pain in Older Adults
Acupuncture, along with other complementary and integrative treatments, is commonly used as a complementary or integrative therapy when treating a multitude of pain complaints, including chronic low back pain(CLBP).
- Trial name
- NCT03850717
- Testing
- acupuncture
- Where
- United States
- Volunteers
- 500 people
- Sponsor
- McLean Center for Complementary and Alternative Medicine, PLC
Migraine Disease
The Migraine and Pain Study GeneBank at Scripps Clinic Registry (MAPS)
The objective of this study is to obtain blood or saliva samples to define genes for migraine and pain diseases.
- Trial name
- MAPS (NCT01004835)
- Where
- United States
- Volunteers
- 61 people
- Sponsor
- Scripps Translational Science Institute
Cervical Spine Degenerative Disc Disease, Fusion of Spine, Cervical Region
Comparison of Outcomes Between Early Physical Therapy Intervention and Usual Care Following Anterior Cervical Fusion Surgery
Background: Early physical therapy (PT) intervention with emphasis on spinal stabilization has been shown to benefit individuals undergoing lumbar spinal surgery.
- Trial name
- ACF (NCT01519115)
- Testing
- early physical therapy intervention, usual care
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Texas Woman's University
Postoperative Pain, Postoperative Nausea
Riskfactors of Post-operative Pain and Nausea After Ambulatory Gynaecological Laparocopy.
Patient due for elective, ambulatory gynaecological laparoscopy will be screened peri-operatively for known and potential risk factors of postoperative pain and nausea/vomiting.
- Trial name
- NCT05050708
- Testing
- Patient interview
- Where
- Norway
- Volunteers
- 300 people
- Sponsor
- Oslo University Hospital
Musculoskeletal Pain, Rheumatologic Disorder
Satisfaction, QoL,Health Status & Clinic Outcomes for Patients Attending MSK Triage Clinics in Rheumatology
The aim of this study is to measure the impact of musculoskeletal (MSK) complaints on the quality of life and general health of MSK Patients attending MSK triage clinics.
- Trial name
- NCT04244968
- Where
- Ireland
- Volunteers
- 325 people, healthy volunteers welcome
- Sponsor
- Health Service Executive, Ireland
Musculoskeletal Disorder, Anxiety Disorders
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
The Norwegian Sickness Absence Clinic (NSAC) Nudge Study is a naturalistic randomized controlled multicentre trial which aim is to measure the efficacy of nudging clinicians' attention towards patients' motivation for work…
- Conditions
- Musculoskeletal Disorder, Anxiety Disorders, Depression, Fatigue
- Trial name
- NSAC (NCT05006976)
- Testing
- NSAC health only, NSAC health + MBW
- Where
- 5 sites in Norway
- Volunteers
- 1,180 people
- Sponsor
- Nordlandssykehuset HF
Cancer Pain, Oncology Pain
Reiki Therapy to Improve Key Symptoms in Integrative Oncology Clinic (REIKI)
The purpose of this research is to investigate the delivery of Reiki to integrative oncology patients and assess its potential for improving cancer-related symptoms in this population.
- Trial name
- NCT06354049
- Testing
- Reiki
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- Case Comprehensive Cancer Center
Pain
Evaluation of Post-PACU Pain Management in Pediatric Surgery
This study aims to assess the differences in overall pain severity, pain management, and satisfaction during recovery period between two groups of children who either receive or do not receive additional education related to…
- Trial name
- NCT02352116
- Testing
- Additional face-to-face education, Standard of care management
- Where
- United States
- Volunteers
- 900 people, healthy volunteers welcome
- Sponsor
- Columbia University
Arthropathy Shoulder, Pain, Acute
CORA-Q15: Continuous vs. Single-injection Interscalene Block on QoR-15 in Outpatient Rotator Cuff Surgery
The purpose of the study will be to compare the efficacy of single-injection interscalene block versus continuous interscalene block on the quality of recovery in patients undergoing outpatient arthroscopic rotator cuff repair…
- Conditions
- Arthropathy Shoulder, Pain, Acute, Anesthesia
- Trial name
- CORA-Q15 (NCT06754657)
- Testing
- Continuous perineural infusion, Single injection
- Where
- Chile
- Volunteers
- 150 people
- Sponsor
- Pontificia Universidad Catolica de Chile
Chronic Pain
Simultaneous Application of Ketamine and Lidocaine During an Ambulatory Infusion Therapy as a Treatment Option in Refractory Chronic Pain Conditions
This study is to retrospective investigate the effects of the simultaneous intravenous (i.v.) administration of lidocaine and ketamine on a four to six weeks interval in treatment refractory different chronic pain conditions.
- Trial name
- NCT05103319
- Testing
- Data collection for statistical analysis to identify patterns of treatment response/ non-response
- Where
- Switzerland
- Volunteers
- 319 people
- Sponsor
- University Hospital, Basel, Switzerland
Fibromyalgia, Chronic Pain
Medical Benefit Evaluation of Ambulatory Activity Combining Rehabilitation and Therapeutic Education, Using an Intelligent Electric Bike for the Health, for the Effort Rehabilitation and the Quality of Life Improvement for Patients Suffering of Moderate Fibromyalgia (FIBROVELIS)
The aim of this study is to decrease the impact of the fibromyalgia on the daily quality of life of the patients suffering of moderate fibromyalgia at 6 months by the practice of an adapted physical activity coupled with…
- Conditions
- Fibromyalgia, Chronic Pain, Adapted Physical Activity, Therapeutic Education
- Trial name
- Fibrovelis (NCT04318054)
- Testing
- Ambulatory activity combining rehabilitation and therapeutic education, using an Intelligent Electric Bike for the Health.
- Volunteers
- 56 people
- Sponsor
- University Hospital, Grenoble