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NCT ID: NCT00522691 Withdrawn - Fecal Incontinence Clinical Trials

Efficacy of Sacral Nerve Stimulation Before Definitive Implantation

SNStest
Start date: September 2007
Phase: N/A
Study type: Interventional

Sacral nerve stimulation (SNS) is an emerging treatment for patients with severe fecal incontinence. The test stimulation is minimally invasive, associated to low morbidity and relatively cheap. On the contrary, implantation of the definite stimulator is related to higher morbidity and considerable costs. A careful patent selection for definite implantation is therefore crucial. However, indication for implantation is actually based only on the subjective criteria reported in the patients´ diary only. Patients and care providers are likely to overestimate the real effect of SNS leading to an unjustified overuse of this expensive device. It is therefore necessary to evaluate real efficacy of SNS during the testing phase in a unbiased setting in order to avoid unnecessary morbidity and costs.

NCT ID: NCT00512044 Withdrawn - Hemorrhoids Clinical Trials

Local Versus General Anaesthesia in Stapled Hemorrhoidectomy

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether local or general anaesthesia in stapled hemorrhoidectomy leads to a shorter operation time with a better patient comfort.

NCT ID: NCT00488384 Withdrawn - Clinical trials for Carcinoma, Squamous Cell

Acitretin Plasma Levels Under Hemodialysis

Start date: June 2007
Phase: Phase 4
Study type: Interventional

Acitretin is given to hemodialysis patients who have developed in-situ or invasive squamous cell carcinoma of the skin in increasing doses up to 25 mg daily for one year.

NCT ID: NCT00383006 Withdrawn - Clinical trials for Stress Disorders, Post-Traumatic

Affect Management Group for Adult Survivors of Childhood Trauma

Start date: May 2006
Phase: Phase 1
Study type: Interventional

Problems of self regulation, e.g. emotional dysfunction, represent a core symptom of adult patients with traumatic childhood experiences. The study intends to evaluate the efficiency of a 14-week group therapy for adult survivors of relational trauma in childhood. Main interventions are psychoeducation about the sequelae of childhood trauma, teaching of skills for affect regulation and techniques for activating resources. The hypothesis is that the group therapy significantly improves the participant's capacity in emotion management and self-soothing.

NCT ID: NCT00324714 Withdrawn - Breast Cancer Clinical Trials

Risedronate in Improving Bone Mineral Density and Bone Health in Postmenopausal Women With Ductal Carcinoma In Situ Enrolled in Clinical Trial CRUK-IBIS-II-DCIS

Start date: February 2003
Phase: Phase 3
Study type: Interventional

RATIONALE: Bisphosphonates, such as risedronate, may help improve bone health and prevent osteoporosis in postmenopausal women. It is not yet known whether risedronate is effective in improving bone mineral density and bone health in women with ductal carcinoma in situ. PURPOSE: This randomized phase III trial is studying risedronate to see how well it works compared to a placebo in improving bone mineral density and bone health in postmenopausal women with ductal carcinoma in situ enrolled in clinical trial CRUK-IBIS-II-DCIS (CRUK: Cancer Research UK) (DCIS: Ductal carcinoma in situ).

NCT ID: NCT00313118 Withdrawn - Healthy Clinical Trials

Mean Values of Oxidative Stress Parameters in Healthy Subjects

Start date: January 2006
Phase: N/A
Study type: Observational

Determination of the mean value of oxidative stress parameters in normals and of the plasma and serum levels, resp. of malondialdehyde, glutathion and superoxide dismutase in healthy subjects.

NCT ID: NCT00284440 Withdrawn - Clinical trials for Primary Open Angle Glaucoma

Choroidal Blood Flow Response to Hand-grip Test in Progressive Glaucoma

Start date: March 2006
Phase: N/A
Study type: Observational

The present study is designed to compare the response of choroidal blood flow to the hand-grip test in glaucoma patients with and without visual field progression.

NCT ID: NCT00003985 Withdrawn - Lung Cancer Clinical Trials

KRN7000 in Treating Patients With Solid Tumors

Start date: September 1998
Phase: Phase 1
Study type: Interventional

RATIONALE: Biological therapies such as KRN7000 use different ways to stimulate the immune system and stop cancer cells from growing. PURPOSE: Phase I trial to study the effectiveness of KRN7000 in treating patients who have solid tumors that have not responded to previous treatment.

NCT ID: NCT00003984 Withdrawn - Clinical trials for Myelodysplastic Syndromes

Monoclonal Antibody Therapy in Treating Patients With Primary Myelodysplastic Syndrome

Start date: February 1999
Phase: Phase 2
Study type: Interventional

RATIONALE: Monoclonal antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. PURPOSE: Phase II trial to study the effectiveness of monoclonal antibody therapy in treating patients who have primary myelodysplastic syndrome.

NCT ID: NCT00003979 Withdrawn - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

CHS 828 in Treating Patients With Solid Tumors

Start date: April 1999
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I trial to study the effectiveness of CHS 828 in treating patients who have solid tumors.