Clinical trials: Patient Reported Outcome
Anal Cancer
Anal Cancer Radiotherapy Study
This is a prospective study of patients receiving radiotherapy or chemoradiotherapy for anal cancer. Treatment effect in terms of survival and local recurrence will be analyzed.
- Trial name
- ANCARAD (NCT01937780)
- Where
- Norway
- Volunteers
- 75 people
- Sponsor
- Oslo University Hospital
End Stage Renal Disease
Ultrafiltration Profiling and Outcomes Among Individuals on Maintenance Hemodialysis
The rate of fluid removal (ultrafiltration, UF) during hemodialysis (HD) may contribute to cardiovascular morbidity and mortality among individuals receiving maintenance HD.
- Trial name
- NCT03301740
- Testing
- UF profiling during HD, Conventional HD
- Where
- 2 sites in United States
- Volunteers
- 34 people
- Sponsor
- University of North Carolina, Chapel Hill
SLE
Prediction of SLE Flares Using Patient-Reported Outcomes and Machine Learning
This study aims to Develop a low-cost, PRO-based ML tool can: - Reduce lab costs - Enable telemedicine monitoring - Detect flares early - Improve care in resource-limited settings.
- Trial name
- SLE-PROM-ML (NCT07890662)
- Testing
- Patient-Reported Questionnaire (PROs)
- Where
- Egypt
- Volunteers
- 500 people
- Sponsor
- Sohag University
Hepatectomy, Pain, Postoperative
Spinal Anesthesia For Enhanced Recovery After Liver Surgery
This project proposes to compare epidural versus spinal anesthesia in patients having liver resection surgery. The investigators hypothesize that spinal anesthesia will result in improved blood pressure control postoperatively…
- Conditions
- Hepatectomy, Pain, Postoperative, Liver Neoplasms
- Trial name
- SAFER-L (NCT03715517)
- Testing
- Continuous thoracic epidural analgesia, Spinal anesthesia with intrathecal morphine, Bupivacaine 0.75% in Dextrose Inj 8.25%
- Where
- Canada
- Volunteers
- 128 people
- Sponsor
- University of Manitoba
Vulvar Atrophy, Vulvovaginal Signs and Symptoms
Retrospective Cohort Study of Symptoms and Quality of Life in Women With Genitourinary Syndrome of Menopause.
The goal of this clinical trial is to retrospectively identify the most prevalent symptoms of genitourinary syndrome of menopause (GSM) among postmenopausal women and to evaluate their impact on quality of life.
- Conditions
- Vulvar Atrophy, Vulvovaginal Signs and Symptoms, Genitourinary Syndrome of Menopause (GSM), Quality of Life
- Trial name
- NCT07737782
- Where
- Spain
- Volunteers
- 100 people
- Sponsor
- Mucosa Innovations, S.L.
IBS
Cl-Pharm-IBS-ML-2026
The purpose of this study is to identify distinct subgroups (phenotypes) of Irritable Bowel Syndrome (IBS) patients. While traditional IBS classification relies mainly on bowel habits, this research uses a multidimensional…
- Trial name
- NCT07809646
- Testing
- Questionnaire and Physical Exam
- Volunteers
- 500 people
- Sponsor
- Tanta University
Acute Pancreatitis
Patient-reported Outcome Scale in Acute Pancreatitis
The PAN-PROMISE study (PAtieNt-rePoRted OutcoMe scale in acute pancreatItis-an international proSpEctive cohort study) aims to measure an outcome variable in acute pancreatitis (AP) based in the patient´s experience.
- Trial name
- PAN-PROMISE (NCT03650062)
- Where
- 26 sites in United States, Colombia and 12 more
- Volunteers
- 525 people
- Sponsor
- Enrique de-Madaria
Physical Activity, Exercise
Physical Activity to Improve Patient Reported Outcomes for Adults With Acute Leukemia
The purpose of this study is to test the efficacy of an evidence-based tailored physical activity program adapted for adults with acute leukemia.
- Conditions
- Physical Activity, Exercise, Acute Leukemia, Consolidation
- Trial name
- Build Stamina (NCT04552912)
- Testing
- Build Stamina Program
- Where
- 2 sites in United States
- Volunteers
- 49 people
- Sponsor
- Duke University
Low Anterior Resection Syndrome
Translation of the International Consensus Definition of LARS Into a Bowl Dysfunction Severity Scoring Tool (New LARS Score)
The purpose of this study is to develop a new severity scoring tool for Low Anterior Resection Syndrome (LARS) drawing on the international consensus criteria for LARS as well as opinions of patients with lived-experience of LARS.
- Trial name
- NCT05605600
- Where
- United Kingdom
- Volunteers
- 8 people
- Sponsor
- Cardiff and Vale University Health Board
Educational Course
A Prospective Patient Education Program for IBD Patients
During the past few decades, key medical organizations have highlighted the importance of patient education and support. Evidence suggests that improving inflammatory bowel disease (IBD) patients' knowledge of their disease may…
- Trial name
- NCT05168345
- Testing
- Course and web information
- Where
- Israel
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Tel-Aviv Sourasky Medical Center
Patient Reported Outcome
Lumbopelvic Movement Control: Effect of Injury History, and the Role of Cortical Control and Its Practical Application 3
Hip and groin pain is a common injury in athletes participating multidirectional sports, and resulting in decreased sports participation and quality of life.
- Trial name
- NCT05177302
- Testing
- HAGOS-C, SF-36v2
- Where
- Taiwan
- Volunteers
- 15 people
- Sponsor
- National Yang Ming Chiao Tung University
Lung Surgery, Chest Tube Removal
Patient Reported Outcomes Targeting Early Chest Tube Removal (PROTECTR) Study
This study is a single centre, prospective clinical trial evaluating the safety and feasibility of implementing a same day chest tube removal protocol in patients undergoing Video Assisted Thoracic Surgery (VATS) anatomical…
- Conditions
- Lung Surgery, Chest Tube Removal, Enhanced Recovery After Surgery (ERAS)
- Trial name
- PROTECTR (NCT06444854)
- Testing
- early chest tube removal
- Where
- Canada
- Volunteers
- 130 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Urinary Incontinence
An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males
This post-market study will assess the performance of and user satisfaction with the PureWick™ Male External Catheter in a home setting.
- Trial name
- PUREST-M (NCT07282860)
- Testing
- PureWick System, UltraFlex Self-Adhering Male External Catheter
- Where
- 15 sites in United States
- Volunteers
- 120 people
- Sponsor
- C. R. Bard
Inborn Errors of Metabolism, Urea Cycle Disorder
Patient and Observer Reported Outcome Measurements in Inborn Errors of Metabolism
lnborn errors of metabolism (IEM) are a heterogeneous group of rare, sometimes debilitating or even fatal diseases . In IEM, both definition and assessment of meaningful outcome parameters is often extremely difficult resulting…
- Conditions
- Inborn Errors of Metabolism, Urea Cycle Disorder, Maple Syrup Urine Disease, Phenylketonurias
- Trial name
- MetaPROM (NCT04248062)
- Testing
- Survey
- Where
- Switzerland
- Volunteers
- 69 people
- Sponsor
- University Children's Hospital, Zurich
Colorectal Carcinoma
ePRO for Adjuvant Therapy of Colorectal Adenocarcinoma
It is a multi-centric randomized controlled trial. The goal of this study is to observe the improvement of QoL using ePRO to manage patients with colorectal cancer who received Oxaliplatin-based adjuvant chemotherapy.The…
- Trial name
- NCT04069455
- Testing
- Electronic Patients Reported Outcomes
- Where
- China
- Volunteers
- 270 people
- Sponsor
- Zhejiang University
Amputation
Patient Reported Outcomes Following Targeted Muscle Reinnervation
The purpose of this study is to characterize the functional status and quality of life of patients undergoing Targeted Muscle Reinnervation (TMR) at time of major limb amputation (primary) or subsequent to major limb amputation…
- Trial name
- NCT04658368
- Testing
- Primary TMR, Secondary TMR
- Where
- United States
- Volunteers
- 2 people
- Sponsor
- University of Wisconsin, Madison
Obesity, Obesity (Disorder)
Quality of Recovery and Patient Satisfaction After Metabolic Surgery at a Tertiary Hospital in Gauteng (QoRPS-MS)
PURPOSE OF THE STUDY?This study aims to assess patients' quality of recovery and satisfaction after metabolic surgery at a tertiary hospital in South Africa using two validated questionnaires.
- Conditions
- Obesity, Obesity (Disorder), Metabolic Disease
- Trial name
- QoRPS-MS (NCT07804290)
- Where
- South Africa
- Volunteers
- 84 people
- Sponsor
- Sefako Makgatho Health Sciences University
Chronic Obstructive Pulmonary Disease (COPD)
Non-interventional Cross-over Study to Reduce Items of PROactive Tools Measuring Physical Activity in Chronic Obstructive Pulmonary Disease (COPD)
The purpose of the protocol is to develop final draft PRO instruments of physical activity in daily life to be used and evaluated in the further validation studies measuring physical activity in chronic obstructive pulmonary…
- Trial name
- NCT01388218
- Where
- 5 sites in Belgium, Greece and 2 more
- Volunteers
- 236 people
- Sponsor
- Barcelona Institute for Global Health
Neuroendocrine Tumors
Lutetium 177Lu-Edotreotide Versus Best Standard of Care in Well-differentiated Aggressive Grade-2 and Grade-3 GastroEnteroPancreatic NeuroEndocrine Tumors (GEP-NETs) - COMPOSE
The purpose of the study is to evaluate the efficacy, safety \& patient-reported outcomes of peptide receptor radionuclide therapy (PRRT) with 177Lu-Edotreotide as 1st or 2nd line of treatment compared to best standard of care in…
- Trial name
- COMPOSE (NCT04919226)
- Testing
- 177Lu-Edotreotide (Peptide Receptor Radionuclide Therapy) PRRT, CAPTEM (Capecitabine and Temozolomide), Amino-Acid Solution
- Where
- 42 sites in United States, Australia and 8 more
- Volunteers
- 259 people
- Sponsor
- ITM Solucin GmbH
Chronic Nonspecific Low Back Pain
Responsiveness of Turkish Disability Questionnaires in Chronic Non-Specific Low Back Pain
This prospective observational clinimetric study aimed to compare the responsiveness of the Turkish versions of the Roland-Morris Disability Questionnaire (RMDQ), Oswestry Disability Index (ODI), and Quebec Back Pain Disability…
- Trial name
- NCT06271460
- Testing
- Standardized Physiotherapy Program
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people
- Sponsor
- Acibadem University
The first 1,020 results can be paged through. Add a filter or change the sort order to reach the rest.