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NCT ID: NCT00531102 Terminated - Resuscitation Clinical Trials

Effect of Establishing Functional Residual Capacity During Newborn Resuscitation on Oxygenation

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

Currently, newborns receive 100% supplemental oxygen by free flow when they remain cyanotic despite demonstrating regular respiratory effort. Resuscitating infants with continuous positive airway pressure (CPAP) in room air may improve oxygen saturations more quickly than providing FFO2 because of its ability to establish functional residual capacity in the lungs. Our primary hypothesis is that in this blinded, randomized control trial, more infants (≥35 weeks gestation) resuscitated with CPAP in room air will have an oxygen saturation ≥80% at five minutes of age compared to infants resuscitated with the 50% FFO2.

NCT ID: NCT00529464 Terminated - Cervical Cancer Clinical Trials

Spectroscopy Versus Standard Care in Cervical Cancer Patients

Start date: November 2006
Phase: Phase 3
Study type: Interventional

Primary objectives 1. To conduct a randomized clinical trial of the emerging technology fluorescence and reflectance spectroscopy, comparing colposcopy to colposcopy + spectroscopy in the diagnostic setting, stratifying patients by outside Papanicolaou (Pap) smear of low grade and high grade squamous intraepithelial lesions, and to use multispectral digital colposcopy retrospectively. The number of clinically read referral Paps, clinically read UT MD Anderson Cancer Center (MDACC) Paps, quantitatively read Paps, quantitatively read biopsies, point probe fluorescence/reflectance spectroscopy, and the multi-spectral digital colposcopy image, that shows a possible cancer, High-grade Squamous Intraepithelial Lesion (HGSIL), Low-grade Squamous Intraepithelial Lesion (LGSIL), or changes less than LGSIL to colposcopically directed biopsies at the first visit, Loop Electrical Excision Procedure (LEEP) at the second visit if needed, repeat evaluations at 6, 12, and 18 months that have Paps, or Paps + Endocervical Curettage or sample of the cervical canal + possible biopsy, and at the 24 month visit when all patients will at minimum have a Pap and an Endocervical Curettage for certain, and a cervical biopsy if any colposcopic abnormality is present. 2. To see if optical spectroscopy using both the point probe and the multi-spectral device improves diagnosis by improving specificity over colposcopy alone. 1. To study the number of colposcopically directed biopsies that show High-grade Squamous Intraepithelial or cancer. 2. To study the number of LEEP specimens that show HGSIL or cancer.

NCT ID: NCT00529386 Terminated - Clinical trials for Chronic Pain Syndrome

Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

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

The objective of this study is to evaluate the safety and efficacy of intraprostatic injection of Botox for the treatment of men diagnosed with chronic nonbacterial prostatitis/chronic pelvic pain syndrome (CP/CPPS).

NCT ID: NCT00528008 Terminated - Wound Infection Clinical Trials

A Comparison of Surgical Preparations and Wound Infection Rates for Elective Cesarean Sections

Start date: December 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to find out if chlorhexidine gluconate solution is better at reducing the rate of wound infection after cesarean section compared to povidone-iodine.

NCT ID: NCT00527696 Terminated - Clinical trials for Stress Urinary Incontinence

Trial Comparing TVT SECUR System and Trans Vaginal Obturator Tape for Surgical Management of Stress Urinary Incontinence

Start date: May 2008
Phase: Phase 3
Study type: Interventional

To compare the efficacy and complications of the TVT SECUR system (TVT S) and trans-vaginal obturator tape (TVT-O) procedures for the surgical management of female stress urinary incontinence.

NCT ID: NCT00524862 Terminated - Clinical trials for Congestive Heart Failure

Standard Drug Therapy vs. Implanted Defibrillator for Primary Prevention of Sudden Cardiac Death

SMART-ICD
Start date: October 2007
Phase: N/A
Study type: Interventional

Recent ACC/AHA/ESC guidelines recommend prophylactic ICD implantation in most patients with coronary heart disease and LVEF < 40%. Current Canadian guidelines recommend ICDs for primary prophylaxis in CAD patients with LVEF < 30% (Class I recommendation). There are very sparse data to recommend ICD implantation in patients with EF between 30 and 40 %. This study will randomize patients with CHD and an EF between 30 and 40% to ICD therapy vs. No ICD therapy. The primary outcome is mortality and the study is powered as a non-inferiority trial to test the hypothesis that mortality in patients with no ICD is not more than 1% greater (absolute yearly increase) than patients receiving an ICD.

NCT ID: NCT00524667 Terminated - Clinical trials for Chronic Lymphocytic Leukemia

HDAC Inhibitor Valproic Acid as an Effective Therapy for Chronic Lymphocytic Leukemia

Start date: January 2008
Phase: Phase 2
Study type: Interventional

OBJECTIVES To investigate: - the mechanism of Valproic Acid (VPA)-induced apoptosis in B-CLL - the ability of VPA in combination with standard chemotherapy or new antitumor agents to induce a synergistic antitumor effect in chronic lymphocytic leukemia (CLL) cells - the clinical efficacy of VPA in previously treated CLL patients. This will be an example of a translational research study where the results of our laboratory studies will be applied to a clinical trial in the CLL clinic at CancerCare Manitoba.

NCT ID: NCT00523471 Terminated - Prostate Cancer Clinical Trials

Blood Test to Measure DNA Damage in Blood

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

To check the radiosensitivity level in individual patients based on their DNA damage level.

NCT ID: NCT00523328 Terminated - Clinical trials for Rheumatoid Arthritis

BG9924 in Combination With Methotrexate Extension of Study 104RA203 (NCT 00458861)

Start date: August 2007
Phase: Phase 2
Study type: Interventional

This study is to observe the long-term treatment of BG9924

NCT ID: NCT00523055 Terminated - Pain Clinical Trials

Ultrasound-guided Supraclavicular Brachial Plexus Blockade

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

Pain Clinic patients undergoing physiotherapy for rehabilitation often have arm freezing performed. The quality of physiotherapy is felt to be superior with good pain control. The quality of the freezing is felt to be better when it is done with ultrasound guidance. We are able to use less drug to achieve the same result. For this reason, we are doing a study to look at the level of freezing drug that accumulates in the body. We feel that the drug levels will be significantly different. We also feel that the time-to-peak drug level will be different than with traditional arm freezing procedures.