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NCT ID: NCT00743769 Withdrawn - Clinical trials for Myocardial Infarction

A Phase 1 Safety Study of the Intravenous Administration of Thymosin Beta in Healthy Volunteers

Start date: April 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether the intravenous administration of single- and multiple-ascending doses of Thymosin Beta 4 is safe and tolerable in healthy volunteers.

NCT ID: NCT00755157 Withdrawn - Clinical trials for Small Cell Lung Cancer

Metronomic Docetaxel and Bevacizumab in Patients With Small Cell Lung Cancer

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

This trial will evaluate the efficacy and safety of metronomic docetaxel and bevacizumab combination in patients with pretreated, advanced small cell lung cancer.

NCT ID: NCT00798798 Withdrawn - Skin Lesion Clinical Trials

Effect of Externally Implantable Tissue Expansion Device on Scar Length

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

The purpose of this study is to assess whether brief use of an externally implantable tissue expansion device following excisional skin cancer surgery will significantly reduce the diameter of the final wound defect, and hence the length of the final linear primary closure. The secondary objective is to assess the functional benefits, if any, associated with use of the tissue expander.

NCT ID: NCT00831831 Withdrawn - Perinatal Outcomes Clinical Trials

Can Safety Planning Improve Perinatal Outcomes Among Pregnant Women Exposed to Intimate Partner Violence?

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

OBJECTIVE: To investigate if, among women exposed to physical violence during pregnancy, does a targeted intervention consisting of safety planning and referral to community advocacy services decrease rates of adverse perinatal outcomes including antepartum hemorrhage or infection, low birthweight, and perinatal death. DESIGN: A randomized controlled trial. SETTING: Surrey Memorial Hospital and BC Women's Hospital in British Columbia, Canada PARTICIPANTS: Pregnant women experiencing intimate partner violence MAIN OUTCOME MEASURES: We are interested in perinatal outcomes such as birth weight and preterm labour. DATA ANALYSIS: Outcomes for women in each arm of the trial will be compared in an intention to treat analysis. Changes in risk for adverse outcomes associated with the study intervention will be estimated by the odds ratios calculated by the logistic regression model.

NCT ID: NCT00915447 Withdrawn - Allergic Rhinitis Clinical Trials

Diesel Exhaust Particles and Leukotriene Production

Start date: April 2008
Phase:
Study type: Observational

The purpose of this study is to measure the effects of allergens and/or diesel exhaust particles in the nose to learn more about allergic responses in individuals with cat allergic rhinitis.

NCT ID: NCT00942396 Withdrawn - Breast Cancer Clinical Trials

Study to Compare the Diagnostic Accuracy of Nuance Full-Field Digital Mammography to Screen-Film Mammography

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

Evaluate the diagnostic accuracy of the Planmed Sophie Nuance Full Field Digital Mammography (FFDM) X-ray System compared to screen-film mammography (SFM) in the detection of breast cancer.

NCT ID: NCT01223599 Withdrawn - Clinical trials for Evaluate and Compare Between Excision and Primary Closure Procedure and Rhomboid Flap Technique for the Treatment of Pilonidal Sinus

Rhomboid Flap Versus Primary Closure After Excision of Sacrococcygeal Pilonidal Sinus. (A Prospective Randomized Study)

non
Start date: April 2008
Phase: N/A
Study type: Observational

To evaluate and compare between excision with primary closure of wound and excision with Rhomboid flap reconstruction in the treatment of pilonidal sinus as regard duration of operation, healing time, hospital stay, complications and recurrence rate.

NCT ID: NCT01307670 Withdrawn - Clavicle Fracture Clinical Trials

Comparison of Nailing, Plate Fixation and Non-operative Treatment of Midshaft Clavicle Fractures

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

Until recently, clavicle fractures have been treated mainly with a sling or brace and felt to have favorable outcomes. Recently, however, data has been published suggesting that these injuries are not as harmless as once thought and, if treated without surgery, may result in lasting functional deficits. As a result, surgery for clavicle fractures is becoming increasingly more accepted as a better treatment option. There are two basic methods of operative treatment. The first involves placement of a metal rod within the middle of the clavicle through a small incision in the skin. Proponents of this technique believe that it has improved cosmetic outcome because of a smaller incision, less post operative pain, and possibly a faster return to activity when compared to other surgical treatments. The second method involves making a larger incision over the clavicle, exposing a large portion of the bone, and fixing the fracture with a plate and screws. Proponents of this method cite better stablity and a decreased risk of the hardware migrating from its intended position among other advantages. This study would propose to determine if these two methods of fracture fixation are necessary and if so, which would provide better outcomes following their use in selected patients.

NCT ID: NCT02369367 Withdrawn - Malignant Gliomas Clinical Trials

Irinotecan Plus Lenalidomide in Adult Patients With Recurrent Glioblastoma Multiforme (Phase II)

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

The goal of this clinical research study is to find the highest tolerable dose of lenalidomide combined with Camptosar (irinotecan) as well as to see if this drug combination can help control malignant gliomas. Researchers will also study if a special magnetic resonance imaging (MRI) technique (dynamic MRI scan) is useful in looking at the effect of treatment on the tumor. Another goal is to learn the effect of lenalidomide on tumor tissue in patients who need surgery for the disease. This record represents the Phase II portion of original Phase I/II study (see registration record NCT00671801).

NCT ID: NCT04802928 Withdrawn - Arterial Leg Ulcer Clinical Trials

Healing of Ischemic Leg Ulcers in Patients Treated With iSONIAzid

SONIA
Start date: April 2008
Phase: Phase 2
Study type: Interventional

The main objective of this trial is to study the healing effect of an oral drug (isoniazid) in patients with ischemic (arterial) leg ulcers defined by a systolic toe pressure <40 mm Hg.