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NCT ID: NCT00957606 Recruiting - Prostate Cancer Clinical Trials

Osteoporosis Among Men Treated With Androgen Deprivation for Prostate Cancer

Osteoporosis
Start date: August 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is - to determine the rate of osteoporosis among patients with advanced prostate cancer. - to propose an algorithm for early detection of patients with advanced prostate cancer who are at risk of developing osteoporosis.

NCT ID: NCT00955539 Recruiting - Heart Failure Clinical Trials

Viability and Cardiac Resynchronization Therapy

Start date: August 2009
Phase: N/A
Study type: Interventional

30% of heart failure patients that receive a device for cardiac resynchronization therapy fail to show clinical improvement. The reason for lack of response is still unclear but factors such as scar tissue in the heart musculature, inadequate lead placement, device-settings and the degree of dyssynchrony before implant seems to be important. In this study, these factors are further investigated.

NCT ID: NCT00935155 Recruiting - Clinical trials for Total Knee Replacement

Effectiveness of Acupuncture as an Adjunct to Rehabilitation After Knee Arthroplasty

Start date: January 2009
Phase: N/A
Study type: Interventional

No randomized trials have tested the effectiveness of acupuncture as a supplement to rehabilitation after total knee replacement. Studies from related fields, however, have shown reduction of symptoms as a result of acupuncture treatment in patients with knee pain caused by severe osteoarthritis in the knee. Furthermore, studies have reported that the need of pain medication was lower when acupuncture treatment was performed immediately after knee surgery. The aim of this study is to test whether acupuncture can reduce pain and improve disability as a supplement to rehabilitation after total knee replacement. One hundred and seventy patients will be allocated by drawing lots to either a treatment group receiving exercise therapy and acupuncture or a group receiving exercise therapy alone. Treatment will start 3 weeks after surgery at the latest. Outcome of treatments will be measured at completion of treatment and at 3 months follow-up by pain- and disability questionnaires as well as the recording of walking capacity.

NCT ID: NCT00928473 Recruiting - Obesity Clinical Trials

The Danish Childhood Obesity Biobank

Start date: January 2009
Phase: N/A
Study type: Interventional

The Danish Childhood Obesity Biobank aims to produce a scientific platform for research in obesity: Bio-clinical data are collected from two cohorts - an obesity clinic cohort and a population-based cohort. The biobank thus facilitates translation between research and clinical practice of obesity treatment and related complications.

NCT ID: NCT00926458 Recruiting - Clinical trials for Coronary Artery Disease

NON-Invasive Examinations of Coronary Artery Disease

NONCAD
Start date: January 2009
Phase: N/A
Study type: Observational

The aim of the study is to evaluate and compare the value of 5 different non-invasive diagnostic methods in patients with chest pain suspected for coronary artery disease. The investigators intend to include 200 patients over a 3 year period in the study. The participants will be recruited from patients referred to coronary angiography at the institution. Before the angiography the participants will (1) test the effect of sublingual Nitroglycerin, (2) give their medical history so mathematical models can estimate the probability of the presence of coronary artery disease, (3) take part in a contrast stress echocardiography and (4) a 2D-strain stress echocardiography and a myocardial scintigraphy. Stenosis found at the angiography will be the gold standard.

NCT ID: NCT00918099 Recruiting - Vaginal Prolapse Clinical Trials

The Use of Avaulta for Anterior Repair

Start date: October 2008
Phase: N/A
Study type: Interventional

Summary: Vaginal prolapse is a well-known disease and is observed in approximately 11% of all postmenopausal women and tending to increase with age. Consequently, many surgical procedures have been developed in order to ensure sufficient support for the bladder, rectum or vaginal vault depending on the site of the defect. However, many procedures are associated with a high recurrence rate up to 40 % even within one to two years after the surgical procedure. Due to the high recurrence rate new methods include the use of mesh, either biologically or synthetic. The latter is a permanent implant and therefore theoretically may result in a long-lasting anatomically correct position of the prolapse. Although the recurrence rate may be lower using a mesh such surgical procedures may be associated with adverse events such as erosions of the vaginal mucosa. Others have observed shrinkage of the vaginal mucosa. However, in these studies large prolene mesh have been used. In contrast the recurrence rate is lowered up to 25%. The above-mentioned advantage of synthetic mesh is however, mostly based on few non-randomised studies. The investigators therefore find it of importance to evaluate whether a surgical procedure using a mesh implant is superior to conventional surgical techniques. The present study is a clinical controlled study where patients with anterior vaginal prolapse are randomised to either a mesh technique or a standard anterior procedure. The present study includes only two more visits at the outpatient clinic after the surgical procedure. Furthermore the patients have to fulfil questionnaires regarding urinary and faecal leakage and sexual habits. Any participation in the study is totally voluntary and the patient may at any time withdraw herself. In any case the patient will receive the investigators' standard treatment.

NCT ID: NCT00898118 Recruiting - Leukemia Clinical Trials

Studying Blood Samples in Young Patients With Cytopenia After a Donor Stem Cell Transplant

Start date: April 2007
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of blood from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. PURPOSE: This research study is looking at blood samples in young patients with cytopenia after undergoing a donor stem cell transplant.

NCT ID: NCT00877838 Recruiting - Migraine With Aura Clinical Trials

Study of the Safety and Effectiveness of NXN-188 for the Acute Treatment of Migraine Attacks With Aura

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The following study is being conducted to explore the safety and effectiveness of a new chemical entity called NXN-188 in subjects with a history of migraine with aura. In this study subjects will treat two attacks of migraine with aura during the aura phase - once with placebo and once with NXN-188.

NCT ID: NCT00864409 Recruiting - Postoperative Pain Clinical Trials

Local Infiltration Analgesia With Ropivacaine Versus Placebo in Bilateral Hip Arthroplasty

Start date: n/a
Phase: Phase 4
Study type: Interventional

High-volume infiltration analgesia may be effective in postoperative pain management following total hip arthroplasty. In this randomized, double-blind trial patients undergoing bilateral hip arthoplasty are randomized to receive high-volume local anesthetic infiltration in one hip and similar infiltration with saline (placebo) in the other hip.

NCT ID: NCT00850850 Recruiting - Clinical trials for Postoperative Nausea and Vomiting

Physostigmine After General Anesthesia

Start date: December 2009
Phase: N/A
Study type: Interventional

Recovery after general anaesthesia is often prolonged in the elderly. This group is particularly exposed to post-operative confusion. This has negative personal consequences as well as consequences for the postoperative care for these patients. The hypothesis is that physostigmine will decrease the amount of time in the post-anaesthesia care unit (PACU ), the postoperative amount of pain and shivering and finally post-operative confusion.