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NCT ID: NCT06358586 Completed - Healthy Clinical Trials

New Paediatric Formulation of Tachipirina®

Start date: April 9, 2022
Phase: N/A
Study type: Interventional

This is a single centre, single dose, single-arm, open-label, palatability study. The aim of the present study is to investigate the palatability of the newly developed Tachipirina® 120 mg/5 mL oral suspension with strawberry flavour. The study will be conducted in paediatric volunteers that represent the target population for this product.

NCT ID: NCT06330259 Completed - Clinical trials for Reproductive Sterility

Does the AMH Concentration Depend on the Menstrual Cycle?

AMH
Start date: July 1, 2017
Phase:
Study type: Observational

During two none subsequent natural menstrual cycles healthy female participants will be subjected every second day to blood sampling and 3D-ultrasound examinations. Together with four other key hormones the concentration of AMH (anti-Muellerian Hormone) will be measured in the serum.

NCT ID: NCT06307210 Completed - Clinical trials for Musculoskeletal Diseases

Is Inpatient Rehabilitation Effective for Very Old Patients?

Start date: January 1, 2020
Phase:
Study type: Observational

The goal of this retrospective longitudinal observational study is to compare the effects of physical and mental performance as well as quality of life in patients with neurological and musculoskeletal disorders. The main question it aims to answer is: Do very old patients benefit in a similar way from inpatient rehabilitation like younger patients? Data from about 2000 patients will be retrospectively analyzed. Functional Independence Measurement (FIM), Timed Up and Go Test (TUG), EuroQol 5 Dimensions (EQ-5D) and Patient Reported Outcomes Measurement Information System (PROMIS) were recorded on admission and discharge. Researchers will compare the age group 75 to 84 and 85 to 99 to see if physical and mental performance as well as quality of life will improve.

NCT ID: NCT06301230 Completed - Surgical Training Clinical Trials

Home- vs. Hospital-based Surgical Training

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study was to assess the effect of training with a personal, portable laparoscopic endo-trainer (PLET) on residents' laparoscopic skills. All participants were randomised to either a home- or hospital-based PLET training group and surgical skill performance was assessed using five laparoscopic exercises. Endpoints consisted ofsubjective and objective assessment ratings as well as exercise time and qualitative data up to 12 weeks. The primary outcome was the difference in exercise time and secondary outcomes included performance scores as well as qualitative data.

NCT ID: NCT06211153 Completed - Clinical trials for Chronic Myeloid Leukemia With T315I Mutation

Real-world Effectiveness of Asciminib and Treatment Patterns in Patients With Chronic Myeloid Leukemia With T315I Mutation - a Chart Review Study of Patients Treated in the Asciminib Managed Access Program (MAP)

Start date: December 31, 2021
Phase:
Study type: Observational

This non-interventional study (NIS) was a retrospective chart review analyzing existing data from patients participating in the asciminib MAP.

NCT ID: NCT06172426 Completed - Psoriasis Clinical Trials

Incidence of Psoriatic Arthritis Among Psoriasis Patients Newly Initiated With Secukinumab in a US Claims Database and a UK Registry

Start date: November 17, 2022
Phase:
Study type: Observational

This was a retrospective cohort study to assess the incidence rate of psoriatic arthritis (PsA) among psoriasis (PsO) patients newly initiated on secukinumab or any biologics/apremilast (small molecule). The analysis was performed in two databases, IBM® MarketScan® database: Commercial Claims and Encounters (CCAE) and Medicare Supplemental Beneficiaries (MDCR) from 01 January 2010 to 30 June 2021 and BADBIR from 01 January 2016 to 01 September 2021.

NCT ID: NCT06157788 Completed - Clinical trials for Shoulder Instability

Cerebral Activation and Apprehension in Patients With Shoulder Instability.

Start date: April 1, 2022
Phase:
Study type: Observational

In a similar study, the investigators demonstrated that shoulder stabilization could allow the brain to partially "recover". Patients with shoulder apprehension underwent clinical and fMRI examination before and one year after shoulder stabilization surgery. Clinical examination showed a significant improvement in postoperative shoulder function compared with preoperative. Coherently, results showed a decreased activation in the left pre-motor cortex postoperatively, demonstrating that stabilization surgery induced improvements both at the physical and at the brain levels, one year postoperatively. Most interestingly, right-frontal pole and right-occipital cortex activity was associated with good outcome in shoulder performance.

NCT ID: NCT06152393 Completed - Neurosyphilis Clinical Trials

Value of an Intrathecal Synthesis Index of Specific Antitreponema IgG for Neurosyphilis Diagnosis

Start date: March 1, 2019
Phase:
Study type: Observational

A retro-prospective case-control Swiss study was conducted to evaluate the diagnostic performance of measuring an antibody index (AI) for intrathecal synthesis of specific anti-Treponema pallidum (T. pallidum) IgG for the diagnosis of neurosyphilis.

NCT ID: NCT06145815 Completed - Rotator Cuff Tears Clinical Trials

Machine Learning Predictive Model for Rotator Cuff Repair Failure

Start date: September 1, 2022
Phase:
Study type: Observational

There is little overall evidence behind clinical practice guidelines for diagnosis and treatment of rotator cuff repair. The purpose of this study was to compare the performance of different machine learning models that use pre-operative data from an international and multicentric database to predict if a patient that underwent rotator cuff repair could achieve the minimal important change (MIC) for single assessment numeric evaluation (SANE) at one year follow-up.

NCT ID: NCT06138392 Completed - Dental Implant Clinical Trials

Long-term Study in Early Loaded Hydrophilic Surface Implants

Start date: September 1, 2020
Phase:
Study type: Observational

Objective: To assess the clinical outcomes and patient satisfaction of early loaded implants with a hydrophilic, moderately rough surface for partially edentulous patients after a follow-up of 8.5 to 9.5 years. Materials and methods: A prospective observational single-centre study involving 15 patients with single, delayed placement and early loaded implants in the posterior area was performed. Clinical and radiographical parameters, including biological and technical complications and patient satisfaction, were assessed.