Clinical trials: Consent of Patients
Cytomegalovirus
Prospective Multicentric Study of Cytomegalovirus Resistance in Transplant Patients and Bone Marrow Recipients
The investigators aim is to determine the incidence of cytomegalovirus resistance to antivirals in a cohort study. The patients are included at their first CMV active infection and are followed during two years thereafter.
- Trial name
- PHRC CMV (NCT01008540)
- Testing
- depistage
- Where
- 33 sites in France
- Volunteers
- 800 people
- Sponsor
- University Hospital, Limoges
Gallstone Disease
Multimedia Informed Consent & PROMs in Laparoscopic Cholecystectomy
Collection of PROMs (Patient Reported Outcome Measures) data from patients before and after an operation to remove their gallbladder for the treatment of symptomatic gallstones.
- Trial name
- EPICS (NCT02810860)
- Testing
- Laparoscopic cholecystectomy
- Where
- United Kingdom
- Volunteers
- 349 people
- Sponsor
- Nottingham University Hospitals NHS Trust
Acceptability of Health Care
The Correlation Between Family Member Presence and The Consent for Regional Anaesthesia for Caesarean Section
Patient's safety and satisfaction are major concerns of anesthesiologists and obstetricians. According to evidence guidelines, and quality markers, regional anesthesia is preferred over general in obstetric surgery.
- Trial name
- BSU (NCT04614220)
- Testing
- Presence of Family member
- Where
- Egypt
- Volunteers
- 110 people
- Sponsor
- Beni-Suef University
Consent Forms, Anesthesia
Effectiveness of Large Language Model for Anaesthesia and Procedural Consent
Patient understanding of anaesthesia risks remains inconsistent due to time constraints, language barriers, and variable clinician communication styles.
- Conditions
- Consent Forms, Anesthesia, Artificial Intelligence (AI)
- Trial name
- PEAR (NCT06949462)
- Testing
- PEAR
- Where
- 2 sites in Singapore
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Singapore General Hospital
Consent Forms of ERCP
Video Consent Form Versus Written Consent Form for ERCP
To prove that video about endoscopic retrograde cholangiopancreatography (ERCP) combined with written informed consent provides participants more information about the procedure, which can make participants understand the…
- Trial name
- NCT02810379
- Testing
- written informed consent, video+written informed consent
- Where
- China
- Volunteers
- 120 people
- Sponsor
- Changhai Hospital
Crohn's Disease
An Open-Label, Proof of Consent Study of Vorinostat for the Treatment of Mdoerate-to-Severe Crohn s Disease and Maintenance Therapy With Ustekinumab
Background: Crohn s disease (CD) is an inflammatory bowel disease. It causes inflammation of the gut. Symptoms may include diarrhea, abdominal pain, fatigue, weight loss and malnutrition.
- Trial name
- NCT03167437
- Testing
- Vorinostat, Ustekinumab
- Where
- United States
- Volunteers
- 35 people
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
Consecutive Subjects Who Are Suitable for a Coronary, Angioplasty of de Novo Lesion(s) in Native Coronary
CRE8 in All Comers Patients
The purpose of the study is to evaluate clinical performances of Cre8 in all comer population in Subjects over 18 years old who are undergoing a clinically indicated coronary angiogram and angioplasty on de-novo lesion located in…
- Conditions
- Consecutive Subjects Who Are Suitable for a Coronary, Angioplasty of de Novo Lesion(s) in Native Coronary, Arteries Should be Screened for Eligibility., A Total Number of 200 Patients Fulfilling the Selection
- Trial name
- NCT01687075
- Testing
- CR8 a drug eluting coronary stent
- Where
- Israel
- Volunteers
- 215 people
- Sponsor
- Tel-Aviv Sourasky Medical Center
Prostate Biopsy
Impact of Procedure Materials on Patient Anxiety, Depression, and Pain in Prostate Biopsy Consent
The gold standard for diagnosing prostate cancer is an ultrasound-guided prostate biopsy. Despite its low complication rates, the procedure can cause significant stress, discomfort and anxiety in patients.
- Trial name
- NCT06802783
- Testing
- Photo consent
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Marmara University
Lung Cancer, Liver Cancer
Observational Study of the Decision Making Towards Clinical Trials in Cancer Patients
This is a cross-sectional, observational and correlational survey study.This study is aim to survey the the knowledge, attitudes, and decision making towards clinical trials in cancer patients in Taiwan (R.O.C.), which attempts…
- Trial name
- NCT01341210
- Where
- Taiwan
- Volunteers
- 116 people
- Sponsor
- National Taiwan University Hospital
HIV Infections
Consent for Use of Stored Patient Specimens for Future Testing
The purpose of this study is to obtain informed consent to use stored human biological materials (HBM) (e.g., blood and other tissues) for future studies that may include genetic testing.
- Trial name
- NCT00031408
- Where
- 63 sites in United States, Puerto Rico
- Volunteers
- 17,444 people, healthy volunteers welcome
- Sponsor
- Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
Cataract and IOL Surgery, VR-based Informed Consent
VR for Cataract Anxiety Lowering Management--A RCT Study
Cataract is currently the leading cause of blindness globally, and surgery is the only effective treatment. With the advancement of medical technology, cataract surgery is usually performed under topical anesthesia, which means…
- Trial name
- VR-CALM (NCT07620821)
- Testing
- Virtual reality simulation of intraoperative audiovisual experience
- Where
- China
- Volunteers
- 223 people
- Sponsor
- Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Adult Patients Ventilated More Than 48 h, Stable Respiratory and Hemodynamic Conditions for SBT
Pulmonary and Cardiac Ultrasound During Weaning From Mechanical Ventilation
Prospective observational clinical multicentric study in ICU with ventilated patients requiring chest ultrasound analysis.
- Conditions
- Adult Patients Ventilated More Than 48 h, Stable Respiratory and Hemodynamic Conditions for SBT, Consent of Patients, Arterial Line
- Trial name
- PULCO (NCT01098773)
- Where
- France
- Volunteers
- 100 people
- Sponsor
- University Hospital, Clermont-Ferrand
Nursing, Family Centered Care
An Exploration of Family Centred Care (FCC) in UK Inpatient Wards
This qualitative study will explore how family-centred care is understood and experienced in adult inpatient medical wards in the UK.
- Conditions
- Nursing, Family Centered Care, Ethics Nursing, Family Nursing
- Trial name
- FCC (NCT07740369)
- Testing
- Semi-structured qualitative interview
- Where
- United Kingdom
- Volunteers
- 30 people
- Sponsor
- Milton Keynes University Hospital NHS Foundation Trust
Schizophrenia, Schizoaffective
Psychiatric Advance Directives for Improved Mental Health Care
During a psychiatric crisis, persons with severe mental illness (SMI) confront complex challenges concerning treatment choices and are often ill equipped or unable to make mental health care decisions.
- Conditions
- Schizophrenia, Schizoaffective, Bipolar Disorder, Stress Disorders, Post-traumatic
- Trial name
- NCT00105794
- Testing
- Psychiatric Advance Directives intervention
- Where
- United States
- Volunteers
- 360 people
- Sponsor
- US Department of Veterans Affairs
Inguinal Hernia, Postoperative Pain
Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain
The study carry out is to determine whether the use of oral pregabalin premedication to assess the analgesic efficacy, opiod sparing, adverse effect and clinical value in post-operative pain management.
- Trial name
- NCT01450345
- Testing
- Pregabalin
- Where
- Malaysia
- Volunteers
- 72 people
- Sponsor
- University of Malaya
Obesity
Comparison Between Celution Preparation and Manual Preparation of Adipocyte Derived Regenerative Cells, Using Stromal Vascular Fraction Cell Counts (COMPARE)
This scientific study is meant to establish correlation in Stromal Vascular Fraction (SVF) cell counts between our manual method of harvesting and Cytori's Celution automated system.
- Trial name
- COMPARE (NCT01127230)
- Where
- Singapore
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Novena Medical Center
Those Who Provided Written Informed Consent, Female Gender
The Effect of a Patient Education Program on Vitamin D Levels and Health Beliefs Regarding Vitamin D Use
Background and Rationale: Vitamin D deficiency is a major public health concern. While clinical guidelines provide treatment protocols, medication adherence remains a significant barrier to achieving target serum levels.
- Conditions
- Those Who Provided Written Informed Consent, Female Gender, Aged 18 Years and Older, Hypothyroidism Disease
- Trial name
- NCT07535671
- Testing
- Educational with vitamin D
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Karadeniz Technical University
Quality of Life
Improving Quality of Life in Nursing Home Residents: A Cluster Randomized Clinical Trial of Efficacy
Improving quality of life (QoL) in residents of nursing homes: A cluster randomized clinical trial of efficacy - The KOSMOS study.
- Trial name
- KOSMOS (NCT02238652)
- Testing
- Communication, Systematic Pain Assessment and Treatment, Medication Review
- Where
- 32 sites in Norway
- Volunteers
- 560 people
- Sponsor
- University of Bergen
Spine Disease, Urologic Diseases
Active Informed Consent: a New Solution to Improve and Objectively Test the Patient Understanding of Complex Surgical Procedures Proposals
This is an interventional, non-pharmacological, randomized controlled superiority study (RCT), multicenter, open label, parallel group.
- Trial name
- NCT06059599
- Testing
- active informed consent
- Where
- Italy
- Volunteers
- 300 people
- Sponsor
- Istituto Ortopedico Rizzoli
Undescended Testis, Anxiety State
The Effect of Using Multimedia During the Informed Consent Process on the Anxiety of Parents of Orchiopexy Patients
Aim: The goal of this randomized controlled trial is to detect the effect of using multimedia during the informed consent process on the anxiety of parents of orchiopexy patients.
- Trial name
- NCT06698081
- Testing
- Video Multimedia
- Where
- Turkey (Türkiye)
- Volunteers
- 70 people
- Sponsor
- Marmara University