Clinical trials: Reported Pain
Postoperative Pain After Total Knee Arthroplasty
Agreement Between Patient-Reported Pain, Observer-Rated Pain Behavior, and Analgesic Request After Total Knee Arthroplasty
The goal of this observational study is to learn how well patients' own pain ratings match what an observer sees and whether the patient asks for extra pain medicine after total knee replacement surgery.
- Trial name
- NCT07891221
- Volunteers
- 120 people
- Sponsor
- Gamze Kübra Zelyurt
Testicular Cancer
Patient Reported Experiences With Sparing External Oblique Fascia Vs Standard Inguinal Orchiectomy
The purpose of this study is to evaluate the difference in patient-reported postoperative outcomes between two standard-of-care surgical techniques for radical orchiectomy (inguinal orchiectomy versus external oblique fascia…
- Trial name
- PRESERVE (NCT06828185)
- Testing
- Radical inguinal orchiectomy, Radical external oblique fascia sparing orchiectomy
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Loma Linda University
Knee Osteoarthritis (Knee OA)
Immediate Effect of Mobilization with Movement on Squat Self-reported Functional Ability, Pain Intensity, and Pain-free Range of Motion in People with Knee Osteoarthritis
Mobilization with movement (MWM) appears to reduce pain, improve knee range of motion, and enhance physical functioning in individuals with knee osteoarthritis (KOA).
- Trial name
- NCT06887868
- Testing
- Mobilization with movement
- Where
- Portugal
- Volunteers
- 40 people
- Sponsor
- Escola Superior de Tecnologia da Saúde do Porto
Chronic Back Pain
Assessing Spinal Pain With an Artificial Intelligence-assisted Whole Body Electrical Stimulation Device
The goal of this observational study is to investigate the correlation between self-reported pain and the measurements obtained using an artificial intelligence-assisted whole-body electrical stimulation device (StimaWELL 120MTRS…
- Trial name
- NCT07244237
- Where
- Turkey (Türkiye)
- Volunteers
- 78 people
- Sponsor
- Amasya University
Urologic Diseases, Patient Satisfaction
Developing a PROM for Recurrent Urinary Tract Infection
This study aims to develop and validate the first set of patient-reported outcome measures for recurrent urinary tract infection (UTI): the Recurrent UTI Symptom Scale and the Recurrent UTI Impact Questionnaire.
- Conditions
- Urologic Diseases, Patient Satisfaction, Pain, Chronic, Sexual Dysfunction
- Trial name
- NCT05086900
- Testing
- Non-interventional Cross-sectional Patient Reported Outcome Measure Development
- Where
- United Kingdom
- Volunteers
- 283 people
- Sponsor
- University of Reading
Pain, Acute, Venous Puncture
Procedural Pain in Children: Intervention With the Hospital Clown
This study evaluates the effect of an intervention with a hospital clown compared to standard care on pain experience for acute hospitalized children receiving venipuncture.
- Conditions
- Pain, Acute, Venous Puncture, Children, Adult
- Trial name
- NCT03366623
- Testing
- Hospital clown, No hospital clown intervention
- Volunteers
- 111 people, healthy volunteers welcome
- Sponsor
- Aalborg University Hospital
Surgical Procedure, Unspecified, Pain, Postoperative
Experimental Pain Reporting Accuracy and Clinical Post-operative Pain
Pain is a subjective experience that differs in intensity from one person to another. Appropriate medical care relies on an accurate assessment of the patients' condition.
- Conditions
- Surgical Procedure, Unspecified, Pain, Postoperative, Ear, Nose, and Throat (ENT) Disease
- Trial name
- NCT03854669
- Testing
- pain reporting accuracy
- Where
- Israel
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Carmel Medical Center
Pain, Postoperative
Providing Standardized Consented PROMs (Patient Reported Outcome Measures) for Improving Pain Treatment
PROMPT aims at improving management of acute and chronic pain by identifying a core set of PROMs (patient reported outcome measures) that are predictive indicators of treatment success in clinical practice and controlled trials.
- Trial name
- PROMPT (NCT03834922)
- Testing
- Prospective data collection
- Where
- Germany
- Volunteers
- 3,322 people
- Sponsor
- Prof. Dr. Winfried Meissner
Neurofibromatosis 1, Plexiform Neurofibromas
Development and Validation of Patient Reported Outcome (PRO) Measures for Individuals With Neurofibromatosis 1 (NF1) and Plexiform Neurofibromas (pNFs)
Background: People with neurofibromatosis 1 (NF1) who have plexiform neurofibromas (pNFs) can have pain that affects their daily lives.
- Trial name
- NCT02544022
- Where
- 6 sites in United States
- Volunteers
- 476 people, healthy volunteers welcome
- Sponsor
- National Cancer Institute (NCI)
IUD Insertion
Comparison of Pain Level During Intrauterine Device (IUD) Insertion Between Conventional and Direct Method
The so-called "direct" method of intrauterine device (IUD) and intraintuerine system (IUS) insertion is increasingly used. A study has shown that it is technically simpler and assumes less painful than the classic pose.
- Trial name
- KIDDS (NCT03473717)
- Testing
- classic method, direct method
- Where
- 10 sites in France
- Volunteers
- 158 people, healthy volunteers welcome
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Role-expectancy on Patient Reported Outcomes
Influence of Role-expectancy on Patient Reported Outcomes Among Patients With Migraine: a Randomized Clinical Trial
This study was preregistered 2019 under https://osf.io/nczhj. Since JAMA requires a registration with ClinicalTrials.gov, we post-register the study here with the identical informations from OSF (see there) Migraine is frequently…
- Trial name
- NCT06322550
- Testing
- cover story
- Where
- Germany
- Volunteers
- 366 people, healthy volunteers welcome
- Sponsor
- Universitätsklinikum Hamburg-Eppendorf
Breast Cancer
Effect of Patient Education on Reported Bone Pain in Breast Cancer Patients Receiving Chemotherapy and Pegfilgrastim
The purpose of this study is to determine if patient education can affect patient reported bone pain in breast cancer patients receiving chemotherapy and pegfilgrastim.
- Trial name
- VINE (NCT01752907)
- Testing
- General Education DVD, Bone Pain Education DVD
- Where
- 51 sites in United States
- Volunteers
- 304 people
- Sponsor
- Amgen
Coronary Artery Disease, Angina Pectoris
Patient-Reported Preferences Affecting Revascularization Decisions
Selection of a treatment strategy for patients with symptoms due to coronary artery disease requires consideration of patient preferences.
- Trial name
- PREPARED (NCT02272062)
- Testing
- Decision-making tool for coronary artery disease treatment
- Where
- United States
- Volunteers
- 203 people
- Sponsor
- Duke University
Abdominal Pain, Gallstone; Colic
RELIEF-pathway in Patients With Upper Abdominal Pain
Upper abdominal pain (UAP) is a common symptom and frequently the reason to visit the hospital. The prevalence of epigastric pain in the Dutch population is estimated to be as high as 37%.
- Conditions
- Abdominal Pain, Gallstone; Colic, Dyspepsia, Irritable Bowel Syndrome
- Trial name
- RELIEF (NCT06002516)
- Testing
- RELIEF-pathway
- Where
- Netherlands
- Volunteers
- 471 people
- Sponsor
- Radboud University Medical Center
Provoked, Localized Vulvodynia, Provoked Vestibulodynia
Provoked, Localized Vulvodynia Treatment With Acupuncture and Lidocaine Pilot Study
The investigators research project is a randomized, controlled, single-blinded, feasibility pilot study. The investigators will study the feasibility of a novel treatment for women with Provoked Localized Vulvodynia (PLV) with…
- Conditions
- Provoked, Localized Vulvodynia, Provoked Vestibulodynia, Vulvar Vestibulitis, Vulvodynia
- Trial name
- NCT01996384
- Testing
- Classical Acupuncture, Non-classical acupuncture, Lidocaine
- Where
- United States
- Volunteers
- 19 people
- Sponsor
- Oregon College of Oriental Medicine
Shoulder Lesions, Shoulder Injuries
Development a New Scale for Assessment Shoulder Problems
The purpose of this study is to develop and psychometrically validate the Shoulder Problems Assessment Scale (SPAS), a culturally grounded patient-reported outcome measure designed to assess shoulder-related functional…
- Conditions
- Shoulder Lesions, Shoulder Injuries, Shoulder Pain
- Trial name
- NCT05391516
- Testing
- Evaluation of shoulder problems
- Where
- Turkey (Türkiye)
- Volunteers
- 450 people
- Sponsor
- Suleyman Demirel University
Osteoarthritis (OA) of the Knee, Knee Pain Arthritis
Imageless Navigation Versus Image-Based Navigation in Robotic-Assisted Total Knee Arthroplasty for Knee Osteoarthritis
The goal of this clinical trial is to learn if imageless navigation is not inferior to image-based navigation in robotic-assisted total knee arthroplasty (RA-TKA) for treating patients with knee osteoarthritis.
- Conditions
- Osteoarthritis (OA) of the Knee, Knee Pain Arthritis, Total Knee Arthroplasty (TKA), Robotic Assisted Arthroplasty
- Trial name
- NCT07522489
- Testing
- Imageless Robotic-Assisted Total Knee Arthroplasty, Image-based Robotic-Assisted Total Knee Arthroplasty
- Where
- Poland
- Volunteers
- 146 people
- Sponsor
- Medical University of Warsaw
Arthritis
Impact of TheraWorx Foam on Symptom Relief in Thumb Arthritis
Thumb carpometacarpal osteoarthritis (CMC OA) affects up to 33% of people over the age of 40, which leads to inflammation, pain, and weakness of the CMC joint.
- Trial name
- NCT03770091
- Testing
- Theraworx
- Where
- 3 sites in United States
- Volunteers
- 40 people
- Sponsor
- John Fowler
Clavicle Fracture, Postoperative Pain
SPSIPB and CPB on Clavicle Surgeries
Clavicular fractures represent a common occurrence often necessitating effective pain management strategies, particularly following surgical interventions.
- Conditions
- Clavicle Fracture, Postoperative Pain, Analgesia
- Trial name
- NCT06269562
- Testing
- Serratus posterior superior intercostal plane block and clavipectoral plane block
- Where
- Turkey (Türkiye)
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Cumhuriyet University
Bruxism, Self-management
Impact of Self-Management Strategies in Self-Reported Bruxism
This study aim to evaluate the effects of a 6-week self-management program on pain, muscle stiffness, and temporomandibular joint (TMJ) functions in sedentary individuals aged 18-40 with bruxism.
- Conditions
- Bruxism, Self-management, Pain, Proprioception
- Trial name
- NCT06914388
- Testing
- Self-Management Strategies
- Where
- Turkey (Türkiye)
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Cyprus International University