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NCT ID: NCT01731964 Withdrawn - Clinical trials for Age Related Macular Degeneration

Study of WA-NG Telescope Prosthesis in Patients With End-stage Age-related Macular Degeneration

Start date: November 2012
Phase: N/A
Study type: Interventional

This is a pilot study to evaluate the safety of the Model WA-NG telescope prosthesis in patients with bilateral moderate to profound central vision impairment due to end-stage age-related macular degeneration.

NCT ID: NCT01724242 Withdrawn - Breast Cancer Clinical Trials

Vaginal DHEA for Women After Breast Cancer

Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

There does not appear to be a consensus regarding the treatment of vaginal dryness in women who have a contraindication to the use of estrogen products. DHEA, when used locally, may improve the symptoms of vaginal dryness due to its chemical properties.

NCT ID: NCT01709240 Withdrawn - Clinical trials for Child Delivery Using an Elective C- Section

Evaluation of the BioWeld1 System as a Method for Surgical Incision Closure

Start date: January 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to assess the safety and performance of the BioWeld1 System procedure for surgical incision closure of the skin in women scheduled for elective C-section procedure.

NCT ID: NCT01696864 Withdrawn - Stroke Patients Clinical Trials

Remote Rehabilitation Via the Internet in Patients After a Stroke - Physical Rehabilitation Using Biofeedback Systems to Improve Upper Extremity Function

Start date: March 2016
Phase: N/A
Study type: Interventional

The objective of this study is to examine monitored rehabilitation therapy over the internet to improve upper limb function for stroke patients. Home rehabilitation for stroke patients will avoid the burden of arrival to the health facilities, making it easier on them and improve their quality of life and the lives of their caregivers. To achieve this goal the investigators will examine the effectiveness and feasibility of home rehabilitation system of upper limb, consisting of ergonomic accessories (hand and arm tutors). The quantitative indices will be based on the quantitative clinical measures that are used in regular evaluations of stroke patients and function and range of motion indices as received from the system.

NCT ID: NCT01696851 Withdrawn - Clinical trials for Wheelchair Rugby Players With Tetraplegia

Physiological and Psycho-social Variables of People With a Spinal Cord Injury Participating in Competitive Rugby in Wheelchairs

Start date: September 2012
Phase: N/A
Study type: Observational

People with Spinal cord injury with tetraplegia suffer from respiratory problem due to weakness of the muscles and because the autonomic system dysfunction. Exercise is one way of preserving and improving physical fitness and directly and indirectly reduce risk factors such as insulin resistance, weight loss and low values of HDL. subjects with spinal cord injury with tetraplegia have limited options for exercise: table tennis, gym, pool and more. Because of the nature of the injury which includes the sympathetic failure, they can not easily get the desired pulse to improve physical fitness. Wheelchair rugby in Canada was developed specifically for people with tetraplegia who could not participate in wheelchair basketball. The game combines short, quick races with different aerobic capabilities. Previous studies have shown that participants in wheelchair rugby Improve anaerobic power, oxygen consumption, physical fitness and daily functioning. Wheelchair rugby improves self-confidence and as a result it affects other areas of life. Another study examined sense of self-efficacy, saw improvement in this index for rugby players in a wheelchair at high levels. In the present study the investigators aim to examine whether regular participation in wheelchair Rugby for a season has more impact than other routine exercise (table tennis, gym, swimming).

NCT ID: NCT01671215 Withdrawn - Fibroids Clinical Trials

Endometrial and Myometrial Changes, With and Without Fibroids

Start date: August 2012
Phase: N/A
Study type: Observational

fibroids are common among women in fertile age. the relation between fibroids and infertility is controversial. our goal is to claculate a ratio between uterine cavity - endometrium & myometrium in normal uterine s and study the interference of the cavity in uterine s with fibroids.

NCT ID: NCT01659528 Withdrawn - Micropenis Clinical Trials

Establishing Nomograms of Penile Length and Width Throughout the Weeks of Pregnancy

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to establish nomograms of penile length and width throughout the weeks of pregnancy.

NCT ID: NCT01651468 Withdrawn - Menorrhagia Clinical Trials

The Effect of the Nutraceutical "Hemofix" on the Coagulation System

Start date: September 2016
Phase: N/A
Study type: Interventional

Hemofix is a herbal formula based on traditional Jewish and far eastern medicine created to assist in wound healing and bleeding arrest. It contains herbs such as Red Clover, Liquorice, Raspberry, Ginger and more. The present study will evaluate the formula on the coagulation system.

NCT ID: NCT01648309 Withdrawn - Aortic Stenosis Clinical Trials

Neuropsychological Testing in Patients Undergoing Transvascular Aortic Valve Implantation

TAVIPSYCH
Start date: September 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the neuropsychological effects of transvascular aortic valve implantation (TAVI). Patients undergoing TAVI usually suffer from congestive heart failure and low cardiac output which may limit their cognitive abilities. TAVI results in significant improvements in cardiac function and therefore may improve cognitive functions. However, TAVI may also be associated with stroke and may therefore have a negative impact on cognition. Therefore, in this study the investigators wish to perform a battery of standardized neuropsychological tests before and after TAVI to test the net effects of TAVI on cognitive performance over time. The investigators plan to include all patients planned to have TAVI in the study and to test them before, 3,7, 30 and 360 days post TAVI with a standardized battery of test.

NCT ID: NCT01631578 Withdrawn - Low Ovarian Reserve Clinical Trials

Improving the Reproductive Outcome of Poor Quality Ova by Injection of Autologous Somatic Mitochondria

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

A prospective randomized controlled trial (RCT) to determine the effect of injecting an autologous somatic mitochondria concentrate, together with the spermatozoon during ICSI, into oocytes of older and or poor prognosis in vitro fertilization (IVF) patients.