Clinical trials: Patient-Reported Outcomes
Paroxysmal Nocturnal Hemoglobinuria
Home Reported Outcomes in PNH
The study aims to longitudinally capture the full spectrum of symptoms, treatment utilization, and overall Health-Related Quality of Life (HRQoL) experienced by PNH patients.
- Trial name
- NCT06411626
- Testing
- PNH-relevant therapies
- Where
- United States
- Volunteers
- 128 people
- Sponsor
- Novartis Pharmaceuticals
Solid Tumor
Artificial Intelligence to Search for Abnormalities in Ambulatory Cancer Patients
During treatment, cancer patients may experience side effects related to their disease but also to the different treatments they receive.
- Trial name
- IASAAC (NCT05412420)
- Testing
- Patient Self-Reporting of Symptoms
- Where
- France
- Volunteers
- 500 people
- Sponsor
- Institut de Cancérologie de Lorraine
Mycobacterium Infections, Nontuberculous
Validation of Patient Reported Outcome Measures in Participants With Nontuberculous Mycobacterial Lung Infection Caused by Mycobacterium Avium Complex
The primary objective of this study is to generate evidence demonstrating the domain specification (via modern psychometric methods), reliability, validity, and responsiveness (within-subject meaningful change) of the…
- Trial name
- ARISE (NCT04677543)
- Testing
- ALIS, Azithromycin, Ethambutol
- Where
- 62 sites in United States, Argentina and 10 more
- Volunteers
- 99 people
- Sponsor
- Insmed Incorporated
Plantar Fasciitis, Chronic
Comparison of Responsiveness of Different Pain and Disability Measurements in Plantar Fasciitis
The aim of the present study is compare the frequently used pain and disability assessment questionnaires before and after 5 sessions of standard treatment for patients admitted to the Physical Medicine and Rehabilitation…
- Trial name
- NCT04271696
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Gaziosmanpasa Research and Education Hospital
Frailty
Outcomes That Matter and Questionnaires for Older People With Frailty
The goal of this qualitative study is to investigate what matters to older people living with frailty, and how this can be measured using questionnaires (Patient Reported Outcome Measures, or "PROMs").
- Trial name
- NCT06099691
- Testing
- Qualitative Interviews
- Where
- United Kingdom
- Volunteers
- 15 people
- Sponsor
- Royal Devon and Exeter NHS Foundation Trust
Cancer
Spanish Translation of the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
The purpose of this study is to see if questions in English about symptoms that patients may have during cancer treatment are understandable when translated into Spanish.
- Trial name
- NCT01436240
- Testing
- questionnaire administration followed by cognitive interviews
- Where
- 6 sites in United States
- Volunteers
- 112 people
- Sponsor
- Memorial Sloan Kettering Cancer Center
Maxillary Deficiency, Head and Neck Neoplasms
Predictors of Patient-Reported Outcomes for Maxillectomy Patients
The success of digitally fabricated obturator rehabilitation is determined not only by the prosthesis itself but also by the interaction between patient characteristics, oncologic history, prosthetic support, and…
- Trial name
- NCT07864974
- Testing
- Digitally Fabricated Obturator Prosthesis
- Where
- Turkey (Türkiye)
- Volunteers
- 75 people
- Sponsor
- Dr. Merve Benli
Ischemic Heart Disease
Early Prediction of Major Adverse Cardiovascular Events Using Remote Monitoring
Usual care may not identify subtle clinical changes that precede a major adverse cardiovascular event (MACE). Therefore investigators will explore the effectiveness of using biomarkers, patient reported outcomes (PROs), and…
- Trial name
- NCT03064360
- Testing
- Laboratory Biomarker Analysis, Patient Activity, Questionnaires
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Cedars-Sinai Medical Center
Breast Cancer
Biological Matrices Versus Synthetic Meshes
In this feasibility study, 60 women undergoing reconstruction will be randomly allocated to receive biological or synthetic mesh and followed for 6 months.
- Trial name
- BIOSYM (NCT05449691)
- Testing
- One-stage immediate breast reconstruction
- Where
- 5 sites in United Kingdom
- Volunteers
- 60 people
- Sponsor
- University Hospitals of Derby and Burton NHS Foundation Trust
Prostatic Neoplasms
Treatment Satisfaction With Ra-223 in Japan
This study aims to answer the research question: Are Japanese bone metastatic CRPC patients satisfied with their Ra-223 treatment, and what factors drive such satisfaction? It also aims to determine patient anxiety regarding…
- Trial name
- NCT03315260
- Testing
- Radium-223 dichloride (Xofigo, BAY88-8223)
- Where
- Japan
- Volunteers
- 85 people
- Sponsor
- Bayer
Pain
Screening Protocol
This study is a screening evaluation for volunteers who are interested in participating in National Center for Complementary and Integrative Health (NCCIH) research studies about pain and related processes, such as emotion, mood…
- Trial name
- NCT07712874
- Where
- United States
- Volunteers
- 10,000 people, healthy volunteers welcome
- Sponsor
- National Center for Complementary and Integrative Health (NCCIH)
Cataract
Clareon TruPlus vs Tecnis Eyhance IOLs in Cataract Patients
This study is a prospective, randomized, two-arm, single-center, single-surgeon, double-masked (subject and assessor) comparative study.
- Trial name
- NCT07658040
- Testing
- Clareon TruPlus, Tecnis Eyhance
- Where
- United States
- Volunteers
- 70 people
- Sponsor
- Gainesville Eye Associates
Antineoplastic Agents
Tablet-based Patient Reported Outcome
This study is a single arm feasibility study. Patients that have been diagnosed with carcinoma and are undergoing chemotherapy have to document chemotherapy associated side effects on a regular basis by means of a tablet-based…
- Trial name
- NCT01991691
- Testing
- Tablet-based questionnaire
- Where
- 3 sites in Germany
- Volunteers
- 57 people
- Sponsor
- University Hospital, Bonn
Edentulous Alveolar Ridge
The Impact of the Adequacy of Keratinized Mucosa on Peri-implant Tissue Health and Patient-reported Outcomes
This study aims to conduct a cross-sectional study to compare the differences in clinical indices, patient-reported outcomes, and levels of inflammatory factors in peri-implant gingival crevicular fluid between sites with…
- Trial name
- NCT07124416
- Testing
- No intervention
- Where
- China
- Volunteers
- 150 people
- Sponsor
- The Dental Hospital of Zhejiang University School of Medicine
Lymphedema Arm, Lymphedema of Leg
LymphAssistTM at Home (LAAH)
Lymphoedema is a life-long condition causing long-term swelling affecting people physically, mentally and socially. Daily self-management covers four main areas (skin care, activity / movement, compression and massage / light…
- Trial name
- LAAH (NCT05456568)
- Testing
- LymphAssistTM Professional
- Where
- United Kingdom
- Volunteers
- 40 people
- Sponsor
- Swansea Bay University Health Board
Hip Fractures, Knee Fracture
Evaluation of Multidisciplinary Recovery After Surgery Program in Orthopedics and Traumatology
The aim of the recovery protocol is to reduce surgical trauma, postoperative pain, and complications, shorten hospital treatment and improve postoperative recovery.
- Conditions
- Hip Fractures, Knee Fracture, Hip Arthritis, Knee Arthritis
- Trial name
- NCT03822247
- Testing
- Multidisciplinary Recovery Program
- Where
- Croatia
- Volunteers
- 100 people
- Sponsor
- Klinički Bolnički Centar Zagreb
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
Parotidectomy, Patient-reported Outcomes
Patient Reported Outcomes Following Parotid Resections
A study correlating patient reported outcomes measured by a validated tool with physical measurements recorded by 3d photography of patients undergoing parotid resections
- Trial name
- NCT03201484
- Testing
- FACE-Q questionnaire, 3D photography
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Guy's and St Thomas' NHS Foundation Trust
Surveys, Usability
Usability and Satisfaction With an Electronic Survey Administration Application in General Population
The goal of the study is to assess the usability and satisfaction of an electronic patient reported outcomes (e-PRO) mobile application.
- Conditions
- Surveys, Usability, Healthy
- Trial name
- CePRO (NCT04102384)
- Testing
- e-PRO App
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Massachusetts General Hospital
Total Hip Arthroplasty
Rehabilitation in Total Hip Arthroplasty Through a Mobile Application
This observational retrospective study aims to assess the rehabilitation outcomes of patients who underwent total hip arthroplasty (THA) and were monitored through a mobile application versus those who were not.
- Trial name
- HIP-App (NCT06606158)
- Testing
- Exercises program, App exercises program
- Where
- Spain
- Volunteers
- 110 people
- Sponsor
- Universidad Pontificia Comillas
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