Clinical trials: Patient-Reported Outcomes
Colorectal Cancer, Breast Cancer
A Research Study to Collect Patient Reported Outcomes Using Electronic Surveys
A single-centre, randomized, 2-arm clinical trial comparing follow-up consisting of tumour-specific Electronic Patient-Reported Outcomes (ePROs) with targeted symptom management versus standard of care follow-up during…
- Trial name
- NCT04990895
- Testing
- Electronic Tumour-Specific Patient-Reported Outcomes (ePRO) questionnaires
- Where
- Canada
- Volunteers
- 8 people
- Sponsor
- AHS Cancer Control Alberta
Chronic Obstructive Pulmonary Disease
Study of Clinical and Patient-reported Outcomes in Adults With Moderate to Severe COPD Treated With Breztri/Trixeo
Chronic Obstructive Pulmonary Disease is a leading cause of global morbidity and mortality, especially in low- and middle-income countries. Exacerbations accelerate disease progression and increase the risk of death.
- Trial name
- iCHOROS (NCT07069829)
- Where
- 36 sites in Argentina, Colombia and 10 more
- Volunteers
- 1,400 people
- Sponsor
- AstraZeneca
Class II Division 1 Malocclusion
Patient-related Outcomes When Accelerating Upper Canine Retraction With Fixed Orthodontic Appliances
Patients will be screened in the Orthodontics Department of the Faculty of Dentistry, Damascus University, and those who meet the inclusion criteria will be included.
- Trial name
- NCT06875037
- Testing
- Electric stimulation removable appliance, Traditional orthodontic fixed appliance without accleration
- Where
- Syria
- Volunteers
- 40 people
- Sponsor
- Damascus University
PROM, PREM
Trends of Patient-reported Outcome Measures (PROMs) in Multimorbid Medical Patients Hospitalized for an Acute Illness
currently, PROMs and PREMs are not routinely collected and compared among medical inpatients of Swiss university hospitals, nor is a standard set of PROMs and PREMs available for use in Swiss hospitals.
- Conditions
- PROM, PREM, Quality of Care, Internal Medicine
- Trial name
- TRADUCE (NCT06597318)
- Testing
- Hospitalization
- Where
- Switzerland
- Volunteers
- 1,000 people
- Sponsor
- University of Lausanne Hospitals
Osteoarthritis, Pain
Efficacy of Exercise on Quality of Life and Physical Function in Patients With Knee Osteoarthritis
The overall contribution of this study is to increase the knowledge of the efficacy of strength and aerobic exercise on knee related quality of life, knee pain, and physical function in patients with knee osteoarthritis (OA).
- Trial name
- NCT01682980
- Testing
- Strength training, Aerobic exercise
- Where
- Norway
- Volunteers
- 207 people
- Sponsor
- Oslo University Hospital
Cancer Survivors, Cancer Survivorship
SBU-RESET: RElaxation, Stress Reduction and Epigenetics Trial in Cancer Survivors
Cancer survivors can experience health issues that cause chronic illness and lower quality of life. Yoga is a well-known holistic approach to health and overall well-being.
- Trial name
- RESET (NCT07161713)
- Testing
- Oncology-informed yoga, SMART
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Barbara Nemesure
Osteoarthritis of the Knee
Effect of Bioskin Ten-7 vs. Standard Treatment on Patient Reported Outcomes and Cytokine.
The objectives of the study are 1.) to evaluate pain relief following the application of the Bioskin Ten-7 knee brace and 2.) to determine if use of the Bioskin Ten-7 knee brace is more effective at reducing inflammation than…
- Trial name
- Bioskin (NCT02295020)
- Testing
- Standard treatment only, Standard treatment plus Bioskin Ten-7 knee brace
- Volunteers
- 40 people
- Sponsor
- Cropper Medical
Fibromyalgia, Pain, Chronic
Pain Severity in Fibromyalgia Syndrome
Fibromyalgia Syndrome (FMS) is a complex syndrome that mainly includes the musculoskeletal system and is characterized by many symptoms such as chronic widespread pain, fatigue and sleep disorders, cognitive dysfunctions…
- Trial name
- NCT05481086
- Testing
- No Interventions
- Where
- Turkey (Türkiye)
- Volunteers
- 93 people
- Sponsor
- Kutahya Health Sciences University
Prostate Cancer
Prostate Cancer Study of Patient Experiences
The PROSPEX (PROstate cancer Study of Patient EXperiences) survey is designed to systematically assess the lived experiences, challenges, and unmet needs of individuals diagnosed with prostate cancer.
- Trial name
- PROSPEX (NCT07096596)
- Testing
- No Intervention: Observational Cohort
- Where
- Turkey (Türkiye)
- Volunteers
- 3,000 people
- Sponsor
- Ankara University
Surgeons, Surgical Procedure, Unspecified
Improving Surgical Communication for Patients in Wisconsin
The purpose of this study is to evaluate a new training program to support communication between surgeons and their patients. The goal of the training program is to help patients get the information they need to make treatment…
- Trial name
- NCT06647303
- Testing
- Training on communication framework, Focus Group, Surveys
- Where
- United States
- Volunteers
- 580 people, healthy volunteers welcome
- Sponsor
- University of Wisconsin, Madison
Oncology, Quality of Life
Measuring Health Related Quality of Life in AYAs
AIM1a: AYAs with cancer experience many challenges that impact their health-related quality of life (HRQOL) but few measures adequately capture AYAs' HRQOL in valid and reliable ways.
- Trial name
- PROMIS AYA (NCT03482778)
- Where
- 3 sites in United States
- Volunteers
- 165 people
- Sponsor
- Wake Forest University Health Sciences
Knee Injuries
Validity and Reliability of the Turkish Version of the Tegner Activity Score
The goal of this observational study is to learn about patients who will undergo anterior cruciate ligament reconstruction. The main questions it aims to answer are: Is the Turkish version of the Tegner Activity Score a valid…
- Trial name
- NCT06571240
- Testing
- Anterior cruciate ligament reconstruction
- Where
- Turkey (Türkiye)
- Volunteers
- 69 people
- Sponsor
- Kırklareli University
Severe Atrophy of the Edentulous Maxilla
"Tunnel" Flap vs Trapezoidal Flap for Lateral Sinus Lift
The goal of this clinical trial is to evaluate the efficacy of the lateral sinus lift procedure using the tunnel technique flap in comparison to the traditional lateral sinus lift in partially or totally edentulous patients with…
- Trial name
- NCT06105489
- Testing
- Lateral Sinus Lift using tunnel flap technique, Lateral Sinus Lift using crestal incision flap
- Where
- Italy
- Volunteers
- 36 people
- Sponsor
- Studio Dentistico Associato Sivolella
Posterior Malleolus Fractures, Ankle Fractures
Weber B Ankle Fractures With Associated Posterior Malleolus Fracture
Ankle fractures constitute 9% of all fractures and have an incidence of approximately 187 per 100,000 persons per year in Norway.
- Conditions
- Posterior Malleolus Fractures, Ankle Fractures, Syndesmotic Injuries, Patient Reported Outcome Measure
- Trial name
- PMFIX (NCT05413707)
- Testing
- Fixation of the posterior malleolus fractures, Fixation of lateral and/or medial malleolus fractures, Syndesmotic fixation
- Where
- Norway
- Volunteers
- 198 people
- Sponsor
- Haukeland University Hospital
Metastatic Renal Cell Carcinoma, Kidney Neoplasm
Individualized Treatment Strategy for Patients With Metastatic Non-clear Cell Renal Cell Carcinoma
The purpose of the open-label INDIGO-study is to examine whether a first line individualized treatment strategy based on DNA and RNA analyses from the patient's tumor is feasible.
- Conditions
- Metastatic Renal Cell Carcinoma, Kidney Neoplasm, Urologic Neoplasms, Urogenital Neoplasms
- Trial name
- INDIGO (NCT04644432)
- Testing
- Medication (A specification is listed under each arm), Patient reported outcomes measurement
- Where
- Denmark
- Volunteers
- 30 people
- Sponsor
- Herlev and Gentofte Hospital
Kidney Transplant, DCD Kidney
NRP + ex Situ HMPO2 vs NRP Alone in DCD Kidney Transplantation
The goal of this clinical trial is to learn if the combination of Normothermic Regional Perfusion (NRP) at the time of organ procurement with ex situ Hypothermic Oxygenated Perfusion (HMPO2) of kidneys recovered from donors after…
- Trial name
- OxyPerf (NCT07779187)
- Testing
- Ex situ hypothermic oxygenated machine preservation
- Where
- 3 sites in Sweden
- Volunteers
- 214 people
- Sponsor
- Karolinska University Hospital
Migraine Disorders, Chronic Migraine Headache
EMBRACE-OBS: Single-Site Observational Registry of Patient-Reported Outcomes Following MMA Embolization for Migraine
EMBRACE-OBS is the first phase of the EMBRACE research program. This single-site observational registry accesses and analyzes patient-reported outcome data already collected through routine clinical care from adults with migraine…
- Conditions
- Migraine Disorders, Chronic Migraine Headache, Migraine
- Trial name
- EMBRACE-OBS (NCT07652034)
- Testing
- Middle Meningeal Artery Embolization
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Cortex Neurovascular
Vascular Malformations, VM - Vascular Malformation
Patient Reported Outcomes for Vascular Malformations EmbolizatioN (PROVEN)
The purpose of this study is to develop a standardized assessment for patients treated for venous malformations (VM). Venous malformations result from the abnormal development of veins which may result in pain, swelling…
- Trial name
- NCT04104464
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Johns Hopkins University
Corneal Abrasions
IN PATIENTS WITH CORNEAL ABRASIONS TREATED WITH COLLAGEN CORNEAL SHIELDS IN THE EMERGENCY DEPARTMENT SETTING
This is a single-center, double-arm, patient masked, randomized controlled trial. Subjects will be enrolled in the Emergency Department at the Penn State Milton S. Hershey Medical Center.
- Trial name
- NCT07225699
- Testing
- Oasis 72-Hour collagen shield
- Volunteers
- 60 people
- Sponsor
- Milton S. Hershey Medical Center
Gynecologic Cancer, Frailty
Cognitive and Physical Frailty as Predictors of Decision Satisfaction in Geriatric Gynecologic Oncology
This prospective observational study aims to evaluate the association between preoperative cognitive function, measured by the Montreal Cognitive Assessment (MoCA), and physical frailty, assessed using the Clinical Frailty Scale…
- Conditions
- Gynecologic Cancer, Frailty, Cognitive Impairment, Geriatric Oncology
- Trial name
- GYNCOGFRAIL (NCT07085000)
- Testing
- No Intervention - Observational Assessment
- Where
- Turkey (Türkiye)
- Volunteers
- 68 people
- Sponsor
- Izmir City Hospital
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