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NCT ID: NCT06224231 Recruiting - Clinical trials for Patient Satisfaction

Patient Survey as a Tool to Quality Assurance and Quality Improvement 2024

Start date: April 2, 2024
Phase:
Study type: Observational

One goal of the investigators of the Department of Anesthesiology and Intensive Care Medicine CCM/CVK, Charité - Universitätsmedizin Berlin is a continuous improvement in the quality of care to the patients. One focus is the freezing preoperatively during surgery, and on the follow-up study to assess the perceived waiting times in the anesthesiology outpatient clinic. The project aims to quality assurance and quality improvement of the CharitéCentrum for Anesthesiology and Intensive Care Medicine 007, Charité - Universitätsmedizin Berlin .

NCT ID: NCT06243978 Recruiting - Hypertension Clinical Trials

Effectiveness of a Digital Health Application for Primary Hypertension (Liebria)

Start date: April 2, 2024
Phase: N/A
Study type: Interventional

This clinical trial with 328 patients with primary hypertension aims to investigate the effectiveness of the self-guided digital application liebria for patients with primary hypertension.

NCT ID: NCT06251024 Recruiting - Healthy Volunteers Clinical Trials

Study of a Respiratory Syncytial Virus Candidate Formulation in Adults Aged 60 Years and Older

Start date: April 2, 2024
Phase: Phase 2
Study type: Interventional

The purpose of this Phase IIb study is to evaluate the efficacy of the RSV vaccine candidate for the prevention of lower respiratory tract disease (LRTD) due to RSV. The study will enroll approximately 4500 adults aged 60 years and older in a 1:1 ratio to receive a single intra-muscular (IM) administration of either a pre-determined dose of the RSV vaccine candidate or placebo.

NCT ID: NCT06253078 Recruiting - Elderly Patients Clinical Trials

Ciprofol EC50 for Inducing Loss of Consciousness in Elderly Patients

Start date: April 2, 2024
Phase: Phase 4
Study type: Interventional

ciprofol is a recently introduced novel sedative drug. In comparison to the traditional propofol, ciprofol exhibits a higher affinity for GABA A receptors, approximately 4-5 times that of propofol, and possesses fewer side effects, particularly notable in respiratory depression and injection pain. In the context of general anesthesia induction, recent research has confirmed a 100% success rate in the induction of general anesthesia for elderly patients (65-80 years old) undergoing non-cardiac surgery with a dosage range of 0.2mg/kg-0.4mg/kg ciprofol. However, for elderly patients aged 65 and above, even up to 85 years old, it is currently not entirely clear what dosage should be selected for patients in different age groups. Consequently, we have designed this trial with the aim of exploring the dosage requirements of ciprofol during general anesthesia induction among elderly patients in various age brackets. Methods: This is a prospective, non-controlled, non-randomized, single-blind study. Elderly patients aged 65 years and older were enrolled in the study with American Society of Anesthesiologists (ASA) physical status I or II undergoing general anesthesia. All patients were divided into five groups according to age, and the corresponding initial dose of ciprofol administered was selected according to the grouping, with subsequent doses of ciprofol determined according to the Dixon up-and-down method. At least seven crossover points were obtained before the conclusion of the study.The primary outcomes were the dose of ciprofol administered at the time of loss of consciousness (mg/Kg) and the plasma concentration of ciprofol.

NCT ID: NCT06253182 Recruiting - Breast Cancer Clinical Trials

Psychosexual Educational Partners Program (PEPP)

PEPP
Start date: April 2, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two Psychosexual Educational programs for women who have completed treatment for breast or gynecological cancer and their partners in preparation for a well-powered phase III study. The investigators plan to enroll 30 dyads in a 2-arm pilot randomized controlled trial (RCT). The primary aim will be to assess the preliminary efficacy of the Psychosexual Educational Partners Program (PEPP) on sexual communication.

NCT ID: NCT06265688 Recruiting - Solid Tumor, Adult Clinical Trials

First In Human Study of CX-2051 in Advanced Solid Tumors

Start date: April 2, 2024
Phase: Phase 1
Study type: Interventional

The purpose of this first-in-human study, CTMX-2051-101, is to characterize the safety, tolerability, and antitumor activity of CX-2051 in adult participants with advanced solid tumors.

NCT ID: NCT06268821 Recruiting - Clinical trials for Type 2 Diabetes Treated With Insulin

Effect on HbA1c of the Initiation of CGM in Adults With Type 2 Diabetes Treated With Basal Insulin in Finland

Start date: April 2, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical study is to determine the impact of starting the use of the FreeStyle Libre 2 glucose monitoring system, over a three month period, on HbA1c in adults with type 2 diabetes treated with a basal insulin regimen.

NCT ID: NCT06274515 Recruiting - Breast Cancer Clinical Trials

A Study to Investigate Mechanisms of Resistance to Breast Cancer Therapies

REMERGE
Start date: April 2, 2024
Phase: Phase 4
Study type: Interventional

This study will evaluate mechanisms of resistance to anti-breast cancer therapies in tumor and blood samples from participants with human epidermal growth factor receptor (HER2) positive, hormone receptor (HR) positive or triple negative breast cancer.

NCT ID: NCT06274697 Recruiting - Clinical trials for Lower Extremity Artery Disease

Validation of a Magnetic Sensor in Arterial Flow Recording, Compared With the Reference Method, at Various Peripheral Arterial Sites

COMADO
Start date: April 2, 2024
Phase: N/A
Study type: Interventional

The measurement of magnetic fields emitted by cardiac activity has already been studied in magneto-cardiography. To date, however, this technology has never been evaluated in the peripheral circulation. The magnetic susceptibility of iron in the circulating blood and the ionic currents in the blood stream generate a very weak induced magnetic current, which can be detected by the micro-sensor of the prototype investigators wish to study. Proving the validity of this prototype would make it a new diagnostic and even prognostic tool, non-invasive, less costly and more accessible than Doppler for screening peripheral arterial disease.

NCT ID: NCT06274775 Recruiting - Anxiety Clinical Trials

Effect of an Educational Nail Biopsy Video on Pre-operative Anxiety, Health Literacy, and Patient Satisfaction

Start date: April 2, 2024
Phase: N/A
Study type: Interventional

The investigators are interested in studying the effect of an animated video depicting a nail biopsy procedure on the anxiety, health literacy, and satisfaction of participants recommended to undergo a nail biopsy procedure. The investigators hypothesize that the animated video will reduce preoperative anxiety, increase health literacy, and increase patient satisfaction in relation to nail biopsy procedures.