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NCT ID: NCT03121794 Completed - Ultrasonography Clinical Trials

Ultrasonographic Identification of the Proximal Humerus Landmarks

Start date: April 1, 2017
Phase:
Study type: Observational

Evaluate whether discrete landmarks of the proximal humerus can be identified using ultrasound in patients with various body habitus and BMI.

NCT ID: NCT03121950 Completed - Dementia Clinical Trials

Movement and Music Intervention for Individuals With Dementia

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The goal of the study is to learn about how possible benefits of movement and music for individuals with dementia. Individuals with dementia will participate in a dance class. The study includes assessments of walking, balance and cognition.

NCT ID: NCT03122171 Completed - Cerebral Palsy Clinical Trials

Use of Low Cost Prostheses to Improve Upper Extremity Function in Children With Cerebral Palsy

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to assess the effectiveness of an upper extremity prosthesis in improving the upper extremity function of children with cerebral palsy who have limited use of their hands. Twelve children, aged 4-17 years, who have cerebral palsy and limitations in their ability to use their hands, will be enrolled. All participants will be fitted with a 3D printed arm/hand prosthesis and receive 8 occupational therapy sessions. Each subject will be evaluated pre-treatment, post-occupational therapy sessions and at 6 months follow-up. The evaluation will include assessment of (1)passive and active arm/hand movement and (2)functional hand skills using several standardized tests. The results from the pre-treatment and the two post-treatment evaluations will be compared.

NCT ID: NCT03123549 Completed - Clinical trials for Cervical Degenerative Disc Disorder

Investigation of the Two Level Simplify® Cervical Artificial Disc

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

This study is intended to demonstrate that the Simplify® Cervical Artificial Disc (Simplify® Disc) is at least as safe and effective as conventional anterior cervical discectomy and fusion (ACDF) when used to treat two contiguous discs from C3 to C7 following discectomy at two contiguous levels for intractable radiculopathy (arm pain and/or a neurological deficit) with neck pain or myelopathy due to abnormalities localized to the levels of the two contiguous disc spaces in subjects who are unresponsive to conservative management.

NCT ID: NCT03125590 Completed - Osteopenia Clinical Trials

Validation, Reliability and Pilot Test of the Personalized Exercise Questionnaire (PEQ)

Start date: April 1, 2017
Phase: N/A
Study type: Observational

The PEQ is the first tool to measure facilitators, barriers, and preferences to exercise in people with osteoporosis.

NCT ID: NCT03126513 Completed - Clinical trials for Gastroparesis Postoperative

Gastric Per Oral Endoscopic Myotomy (G-POEM) in Refractory Gastroparesis

G-POEM
Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Refractory gastroparesis is a disease characterized by a delayed gastric emptying without a mechanical obstruction. Actual treatments have a limited efficacy and gastric per-oral endoscopic myotomy (G-POEM) is a new treatment that has demonstrated initial promising results in these patients. The investigators aims are to evaluate security and efficacy of this endoscopic treatment in participants with refractory gastroparesis.

NCT ID: NCT03126552 Completed - Clinical trials for Necator Americanus Infection

Establishing a Controlled Human Hookworm Infection Model at Leiden University Medical Center

CHHIL
Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Four healthy hookworm-naive volunteers will be exposed to 50 L3 Necator americanus larvae once and will retain infection for up to 2 years.

NCT ID: NCT03127839 Completed - Shoulder Pain Clinical Trials

Type of Exercise and Education in Patients With SubAcromial Pain Syndrome

SAPS
Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Patients seeking care for shoulder pain will be recruited to enroll will be randomized to one of four combined treatment groups; eccentric or traditional strengthening alone and eccentric or traditional strengthening with pain neuroscience education. Patients will be followed for 1 year.

NCT ID: NCT03131791 Completed - Clinical trials for Post-Stroke Upper Limb Spasticity

Comparing the Radial Extracorporeal Shock Waves and Botulinum Toxin Injection for Spasticity

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Botulinum toxin type A (BoNT-A) is widely used in the clinics to reduce spasticity and improve upper limb function for post-stroke patients. However, there were no studies to compare the effect of rESWT and BoNT-A injection for treatment on spasticity.

NCT ID: NCT03131830 Completed - Delivery Mode Clinical Trials

Individual Choice of Delivery Mode

Start date: April 1, 2017
Phase:
Study type: Observational

The primary aim of the study is to investigate personal attitudes regarding mode of delivery among both medical health care professionals and non-professionals. The investigators are also investigating whether providing detailed information that might influence one's decision regarding mode of delivery (such as education on pelvic floor disorders or advantages or disadvantages of epidural anaesthesia) will change participants´ opinion how to determine their preferred mode of delivery.