Clinical trials: Clinical Documentation
Rare Diseases
Rare Tumours in Children and Adolescents (STEP)
The aim of the STEP registry is to collect and evaluate experience and data on the diagnosis and treatment of rare childhood tumors in order to use the knowledge gained to improve the treatment prospects for our patients.
- Trial name
- STEP 2 0 (NCT05773651)
- Testing
- Data collection
- Where
- Germany
- Volunteers
- 10,000 people
- Sponsor
- University Hospital Tuebingen
Hemophilia A
Non-interventional Post-authorisation Study to Document the Immunogenicity, Safety, and Efficacy of NUWIQ
Prospective, multinational, non-interventional post-authorisation study to collect additional clinical data and to ensure consistency in the long-term between the outcome from pre-authorisation clinical studies (in 135 previously…
- Trial name
- NCT02962765
- Where
- 39 sites in United States, Argentina and 11 more
- Volunteers
- 80 people
- Sponsor
- Octapharma
Neoplasms, Clinical Documentation
Ambient AI Documentation in Oncology Consultations
This study tests whether an artificial intelligence (AI) system can help doctors write medical notes during cancer consultations.
- Conditions
- Neoplasms, Clinical Documentation, Artificial Intelligence in Medicine
- Trial name
- NVC-AI-DOC (NCT07850700)
- Testing
- Ambient AI documentation system
- Where
- Lithuania
- Volunteers
- 250 people
- Sponsor
- National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos
Stroke
An Ischaemic Stroke Observational Study
A non-interventional observational clinical study to document the clinical course of patients at 12 months or more following an ischaemic stroke
- Trial name
- NCT03333980
- Where
- 7 sites in United Kingdom
- Volunteers
- 39 people
- Sponsor
- ReNeuron Limited
Inpatient Facililty Diagnoses
Automated Documentation of Vital Parameters Using Mobile Stations and Activation of the Rapid Response Team
The documentation of vital signs is traditionally performed manually when the patient is not admitted in intensive care units, which can lead to documentary errors, long time for data acquisition and, consequently, impairment in…
- Trial name
- NCT04648579
- Testing
- Hillrom, Control
- Where
- Brazil
- Volunteers
- 231 people
- Sponsor
- Hospital do Coracao
Clinical Decision-Making, Decision Making, Computer-assisted
A Study to the Impact of Accuracy Problem Lists in Electronic Health Records on Correctness and Speed of Clinical Decision-making Performed by Dutch Healthcare Providers
The primary objective of this study is to determine whether patient records with complete, structured and up-to-date problem lists ('accurate problem lists'), result in better clinical decision-making, compared to patient records…
- Conditions
- Clinical Decision-Making, Decision Making, Computer-assisted, Medical Records, Problem-Oriented, Quality of Health Care
- Trial name
- ADAM's APPLE (NCT05657002)
- Testing
- patient A with accurate problem list, patient B with inaccurate problem list, patient A with inaccurate problem list
- Where
- Netherlands
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- Eva Klappe
Multiple Sclerosis, Relapsing-Remitting
A Trial for Evaluating Both Safety and Preliminary Efficacy of a Single Infusion of Stimulated Autologous CD4+T Cells in Patients With Relapsing- Remitting Multiple Sclerosis
The purpose of this study is to assess the safety and the preliminary efficacy of a single infusion of stimulated autologous CD4+ T cells in patients with Relapsing-Remitting Multiple Sclerosis.
- Trial name
- SCLEROLYM (NCT02427776)
- Testing
- Autologous CD4+T cells stimulated and expanded ex vivo by a MOG peptide modified by the introduction of a thioreductase motif into the flanking residues of the T cell epitope
- Where
- 3 sites in Belgium
- Volunteers
- 2 people
- Sponsor
- Imcyse SA
Hyperlipidemia
Compliance With Treatment For Patients With Hyperlipidemia
It is a prospective observational study. Patients will be high risk patients (for developing cardiovascular events) that are treated with a statin.
- Trial name
- COLL (NCT00828945)
- Testing
- Lipid Self Test
- Where
- 17 sites in Sweden
- Volunteers
- 259 people
- Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Multiple Sclerosis, Relapsing-Remitting
A Study Investigating the Utilization, Effectiveness and Quality of Life in Clinical Practice in Germany for Participants With Relapsing-remitting Multiple Sclerosis Treated With Ozanimod (Zeposia®)
The purpose of this study is to collect real-world data and to gain insights about long-term usage of ozanimod (Zeposia ®), its effect on well-defined outcome parameters comprising participant-relevant outcomes, as well as…
- Trial name
- OzEAN (NCT05335031)
- Testing
- Ozanimod
- Where
- Germany
- Volunteers
- 450 people
- Sponsor
- Bristol-Myers Squibb
Nursing Documentation Burden
Ambient AI for Reducing Nursing Staff Documentation Time
The goal of this clinical trial is to learn whether using Ambient Artificial Intelligence for nursing staff documentation in an inpatient setting will reduce the time spent in flowsheet documentation and enhance nurse staffing…
- Trial name
- NCT07456241
- Testing
- Artificial Intelligence
- Where
- United States
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- University of Wisconsin, Madison
Biomarker Feedback, Smoking Cessation
Clinical Response to Biomarker Documentation of Child Secondhand Smoke Exposure
1. To do formative work with healthcare providers, clinic staff and parents to develop a protocol for a clinic system to routinely collect blood from children at risk of SHS exposure conduct laboratory testing for tobacco…
- Conditions
- Biomarker Feedback, Smoking Cessation, Secondhand Smoke Exposure, Provider Behavior
- Trial name
- NCT01145729
- Testing
- Biomarker Feedback
- Where
- United States
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- National Institutes of Health (NIH)
Rehabilitation, Clinical Reasoning
RTSS Adoption Into Physiotherapists Documentation
The Rehabilitation Treatment Specification System (RTSS) is a framework that aims to support clinicians in reasoning and documenting how to deliver rehabilitation.
- Conditions
- Rehabilitation, Clinical Reasoning, Medical Record Documenation
- Trial name
- NCT07038694
- Testing
- Qualitative semi structured interview
- Volunteers
- 16 people, healthy volunteers welcome
- Sponsor
- King's College London
AI-assisted Documentation
Effect of AI Assisted Documentation in Primary Health Care on Time Saving, Patient Satisfaction and Health Care Provider Satisfaction
Background There is currently no research evidence from randomized trial settings on the effectiveness of AI-assisted documentation.
- Trial name
- NCT06836258
- Testing
- AI assisted documentation
- Where
- Finland
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Helsinki University Central Hospital
Automated Clinical Documentation
Dragon Ambient eXperience (DAX) Copilot Evaluation
AI solutions like, Dragon Ambient eXperience (DAX) Copilot (Nuance/Microsoft), hold the potential to significantly enhance provider and patient interactions and alleviate pain points that contribute to burn out.
- Trial name
- DAX (NCT06329427)
- Testing
- Dragon Ambient eXperience (DAX) Copilot
- Where
- 5 sites in United States
- Volunteers
- 238 people
- Sponsor
- Wake Forest University Health Sciences
Chronic Low-back Pain, Herniated Disc
LISA Post Market Clinical Follow-Up Study: Documentation of Clinical Outcomes After Surgery With LISA Implant
The study is a post-market surveillance study of the Lumbar Implant for Stiffness Augmentation (LISA), a medical device, which is used to treat low-back pain that accompanies degenerative lesions of grades II, III, and IV…
- Conditions
- Chronic Low-back Pain, Herniated Disc, Degenerative Disc Disease, Lumbar Canal Stenosis
- Trial name
- LISA-PMCF (NCT04631133)
- Testing
- Lumbar Implant for Stiffness Augmentation (LISA)
- Where
- 5 sites in Denmark, France and 1 more
- Volunteers
- 136 people
- Sponsor
- BACKBONE
Localized, Primary Osteoarthritis, Post-traumatic Arthrosis of Other Joints, Shoulder Region
Clinical Outcomes in Shoulder Hemi-arthroplasty Using a PyC Spherical Interpositional Implant
The INSPYRE implant is a new range of shoulder hemi-arthroplasty device. It consists of a Pyrocarbon spherical interpositional implant and is indicated in primary surgery to relieve severe pain or significant disability caused by…
- Conditions
- Localized, Primary Osteoarthritis, Post-traumatic Arthrosis of Other Joints, Shoulder Region, Avascular Necrosis of the Head of Humerus
- Trial name
- NCT02424760
- Testing
- Shoulder hemi-arthroplasty
- Volunteers
- 67 people
- Sponsor
- Stryker Trauma and Extremities
Cushing Syndrome
Observational Registry on Patients With Endogenous CS to Document Safety and Effectiveness of Ketoconazole.
This is a non-interventional, prospective, multinational, multicentre, observational study, in which data collected are those derived from routine clinical practice via an European registry on CS: ERCUSYN.
- Trial name
- KetoPASS (NCT04872920)
- Where
- 6 sites in Croatia, France and 2 more
- Volunteers
- 200 people
- Sponsor
- HRA Pharma
Clinical Documentation, Artifical Intelligence
Effectiveness of an AI Scribe Compared to Routine Templates for Clinical Documentation in Orthopedic Consultations
This randomized study compares AI-generated clinical documentation with traditional dictation templates during orthopedic consultations.
- Trial name
- NCT07489469
- Testing
- AI Medical Scribe, Routine Dictation Template
- Where
- Canada
- Volunteers
- 200 people
- Sponsor
- University of Saskatchewan
Incontinence-associated Dermatitis, Moisture Associated Skin Damage
Seeing Red: Clinical Assessment Tools for Clinical Trial Decision Support
This research aims to assess the utility and validate the inter-rater reliability of the new nursing documentation tools for commonly encountered moisture-associated skin damage including (incontinence-associated dermatitis (IAD)…
- Conditions
- Incontinence-associated Dermatitis, Moisture Associated Skin Damage, Intertrigo
- Trial name
- NCT05760469
- Testing
- Screening
- Volunteers
- 20 people
- Sponsor
- Scotiaderm
Pain
CytoQuel: Clinical Documentation on Effects on Chronic Pain, Wellness, and Reduction of Inflammatory Markers
The purpose for this protocol is to perform an open-label parallel-arm clinical study in healthy subjects to evaluate the efficacy of a nutraceutical product on chronic pain, vascular health, inflammation, and overall wellness.
- Trial name
- NCT03690609
- Testing
- CytoQuel
- Where
- United States
- Volunteers
- 21 people, healthy volunteers welcome
- Sponsor
- Natural Immune Systems Inc