Clinical trials: Pain, completed
Pain
Evaluation of the Role of Tramadol 50mg as an Analgesic During Outpatient Hysteroscopy
The purpose of this study is to evaluate the role of Tramadol 50mg in reducing pain during outpatient hysteroscopy.
- Trial name
- NCT02068209
- Testing
- Tramadol
- Where
- Egypt
- Volunteers
- 140 people
- Sponsor
- Cairo University
Ocular Pain, Dry Eye Syndrome
Dose-finding Study to Assess the Safety and Effect of SYL1001 in Patients With Ocular Pain
The aim of this pilot study is to compare the analgesic effect of two strengths of SYL1001 eye drops versus placebo in patients with ocular pain associated with Dry Eye Syndrome. General and local tolerability are also evaluated.
- Trial name
- NCT02455999
- Testing
- SYL1001
- Where
- 6 sites in Estonia, Spain
- Volunteers
- 66 people
- Sponsor
- Sylentis, S.A.
Painful Diabetic Neuropathy
A Phase 2, Multicenter, Randomized, Double-blind, Placebo Controlled Study for the Pain of Diabetic Peripheral Neuropathy
Primary Objective: To evaluate the efficacy of SKL11197 for the treatment of diabetic peripheral neuropathy pain (DPN). Secondary Objective: To evaluate the safety and tolerability of SKL11197 in subjects with painful diabetic…
- Trial name
- NCT01521598
- Testing
- SKL11197
- Where
- 13 sites in United States
- Volunteers
- 128 people
- Sponsor
- SK Life Science, Inc.
Temporomandibular Joint Disorders
Miofascial Release and Exercises Therapy in the Treatment of Temporomandibular Disorders
Objectives: The aim of this research is to compare the effectiveness of myofascial release therapy and exercise therapy on pain, quality of sleep, anxiety, trigger points, and joint sounds in individuals with temporomandibular…
- Trial name
- NCT02540863
- Testing
- myofascial release protocol and Rocabado exercise therapy, exercise therapy
- Volunteers
- 64 people
- Sponsor
- Universidad de Almeria
Postoperative Pain
Psychometric Testing of the Norwegian Version of the Comfort Behavioral Scale
The purpose of this study is to establish reliability and validity of the Norwegian version of the Comfort behavioral scale.
- Trial name
- NCT01181687
- Where
- Norway
- Volunteers
- 50 people
- Sponsor
- Sykehuset Telemark
Headache Disorder
Headaches: Effects on Sleep, Sensitization, and Psychological Factors
Headache is one of the most common health problems in the society and negatively affects the quality of life of individuals. Increasing complaints of headache in recent years can be associated with many physiological and…
- Trial name
- NCT06603493
- Testing
- Assessment of sleep disorders, Assessment of Central Sensitization, Assessment of depression, anxiety and stress levels
- Where
- Turkey (Türkiye)
- Volunteers
- 132 people, healthy volunteers welcome
- Sponsor
- Nagihan Acet
Post-mastectomy Pain Syndrome
Comparison of Kinesiotaping and Graded Exposure Therapy on Kinesiophobia in Post-Mastectomy Patients
The aim of this research is to compare the effect of Comparison of Kinesiotaping and Graded exposure therapy on Kinesiophobia in Post-Mastectomy patients. The sample size was 30.
- Trial name
- NCT06658314
- Testing
- Experimental interventional group 1(Kinesiotaping), Experimental interventional group II (Graded exposure therapy)
- Where
- Pakistan
- Volunteers
- 32 people
- Sponsor
- Riphah International University
Patellofemoral Pain Syndrome
Therapeutic Effect of Two Muscle Strengthening Programs in Patients With Patellofemoral Pain Syndrome
Introduction: The patellofemoral pain syndrome (SPF) is one of the most frequent pathologies generated by the knee joint. Conservative treatment with physiotherapy exercises reduces pain and improves functional capacity in the…
- Trial name
- NCT04011436
- Testing
- Strengthening program
- Where
- Colombia
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Universidad Nacional de Colombia
Rotator Cuff Tear
A Selective COX-2 Inhibitor Provides Pain Control But Hinders Healing Following Arthroscopic Rotator Cuff Repair
Selective cyclooxygenase (COX)-2 inhibitors are commonly used analgesics that provide similar analgesia but reduced adverse effects compared to other analgesics.
- Trial name
- NCT02850211
- Testing
- Celecoxib, Ibuprofen, Tramadol
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Seoul National University Bundang Hospital
Pain
Assessment of Pain With Insertion of the Foley Catheter for Induction of Labour
The purpose of this study is to assess pain in women randomised to digital or speculum placement of a Foley catheter. Pain during cervical ripening with the Foley catheter is also to be evaluated as well as maternal satisfaction…
- Trial name
- NCT01235364
- Testing
- Foley catheter
- Where
- Sweden
- Volunteers
- 42 people
- Sponsor
- Uppsala University Hospital
Low Back Pain
Accuro Versus Traditional Landmark Palpation Technique to Determine Accurate Spinal Level for Procedures
Currently, at UVA, handheld ultrasound devices (like those used to view an unborn baby) are only two dimensional. The Accuro is a three dimensional handheld ultrasound device.
- Trial name
- NCT02862964
- Testing
- identify L4/L5
- Where
- United States
- Volunteers
- 106 people
- Sponsor
- University of Virginia
Pelvic Floor Muscle Spasm
Addition of Pudendal Blocks to Pelvic Floor Physical Therapy for the Treatment of Pelvic Floor Tension Myalgia
Pelvic floor tension myalgia (PFTM) is increasingly noted in patients with chronic pelvic pain. Pelvic floor physical therapy is typically utilized and is at times combined with other therapies such as botox injections, trigger…
- Trial name
- NCT00928564
- Testing
- Pudendal block
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- University of California, Irvine
Back Pain
BACk Pain in Elders in Norway (BACE-N)
An international Consortium (BACk pain in Elders: BACE) was established in 2008 in order to create standardised methodology for large cohort studies and share data on the burden of back pain in older people.
- Trial name
- BACE-N (NCT04261309)
- Testing
- Usual care
- Where
- Norway
- Volunteers
- 452 people
- Sponsor
- Oslo Metropolitan University
Pain, Postoperative
Phase 3 Study of Efficacy and Safety of the XaraColl® Bupivacaine Implant After Hernioplasty
This is a Phase 3, multicenter, randomized, double-blind, parallel-group, placebo-controlled efficacy and safety study of postoperative pain in adults who are scheduled for unilateral inguinal hernioplasty via open laparotomy…
- Trial name
- MATRIX-1 (NCT02523599)
- Testing
- XaraColl
- Where
- 23 sites in United States
- Volunteers
- 305 people
- Sponsor
- Innocoll
Postoperative Pain, Inflammation
Assessment of the Operative Course in Connection With Removal of Lower Third Molars
The aim of this study is to compare postoperative complications after removal of lower third molars using two different types of anaesthetics and two different treatments against swelling and inflammation (methylprednisolone and…
- Trial name
- NCT00805298
- Testing
- methylprednisolone, xyloplyin adrenalin, marcain adrenalin
- Where
- Denmark
- Volunteers
- 154 people, healthy volunteers welcome
- Sponsor
- University of Aarhus
Cannulation Pain
The Effect of Transcutaneous Electrical Nerve Stimulation on Pain During Venous Cannulation
The purpose of this study was to investigate whether transcutaneous electrical nerve stimulation (TENS) could reduce pain during cannulation of vein.
- Trial name
- NCT01607463
- Testing
- Transcutaneous electrical nerve stimulation (Empi, USA)
- Volunteers
- 100 people
- Sponsor
- Kyungpook National University Hospital
Coronary Artery Disease
Efficacy and Safety Study of Binodenoson in Assessing Cardiac Ischemia
Binodenoson (an experimental drug) and adenosine (an FDA-approved drug that is currently used by doctors) are used to increase blood flow to the heart just like when a person exercises on a treadmill.
- Trial name
- VISION-302 (NCT00944294)
- Testing
- binodenoson, adenosine
- Volunteers
- 419 people
- Sponsor
- Pfizer
Pregnancy
The Role of Timing of Dexamethasone Administration on Pain Scores and Quality of Recovery in Cesarean Section.
The purpose of our study was to evaluate the hypothesis that single dose dexamethasone given sixty minutes preoperatively reduces visual analog scale (VAS) pain scores and improves quality of recovery in patients undergoing…
- Trial name
- NCT02112422
- Testing
- Control, Intervention
- Where
- 2 sites in Canada
- Volunteers
- 40 people
- Sponsor
- University of Manitoba
Neuropathic Pain, Complex Regional Pain Syndromes (CRPS)
Sub-threshold DRG Stimulation vs Sham in Established Responders
The goal of this clinical trial is to learn if sub-threshold dorsal root ganglion (DRG) stimulation provides pain relief beyond placebo in adults with chronic neuropathic pain who already have an implanted DRG stimulator.
- Conditions
- Neuropathic Pain, Complex Regional Pain Syndromes (CRPS), Causalgia, Chronic Pain
- Trial name
- DRG-SHAM (NCT07170722)
- Testing
- Subtreshhold DRG-S
- Where
- Sweden
- Volunteers
- 20 people
- Sponsor
- Umeå University
Chronic Pain
Effect of Wearable Health Technology on Patients Treated for Chronic Pain at Geisinger Health System
This is a proof of concept study to measure the effect of Wearable Health Technology (WHT), including the Apple Watch, iPhone, Pain App and Provider Dashboards on important clinical outcomes in patients treated for chronic pain.
- Trial name
- NCT03299556
- Testing
- WHT
- Where
- United States
- Volunteers
- 420 people
- Sponsor
- Purdue Pharma LP
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