Clinical Trials Logo

Filter by:
NCT ID: NCT00345527 Withdrawn - Anger Clinical Trials

A Randomized Control Trial Examining Two Treatments for Problem Gambling

Start date: n/a
Phase: N/A
Study type: Interventional

Despite evidence of high rates of concurrent substance use and anger problems among problem gamblers, until recently there have been no empirically evaluated treatments for these co-morbid problems. A recent study (Korman, Collins, McMain, & Skinner, 2005) found that an emotion and behaviour regulation treatment (EBRT) was more effective than a gambling-only treatment-as-usual in engaging clients in treatment and in reducing gambling, anger, and substance use. This study is a replication of Korman et al's study and will compare an emotion and behaviour regulation treatment (EBRT) for problem gambling, anger and substance use to a manualized cognitive behavioural treatment (CBT) for problem gambling.

NCT ID: NCT00347256 Withdrawn - Clinical trials for Paranasal Sinus Neoplasms

Chemoradiotherapy Followed by Surgery for Advanced Paranasal Sinus Cancer

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of concurrent chemotherapy and radiotherapy pre-operatively in patients with advanced paranasal sinus cancer. The main objectives of this study are: 1) to measure the rate of complete response to preoperative chemoradiation and 2) to study the efficacy of combining preoperative chemoradiation and surgery in terms of local control of the cancer two years post treatment.

NCT ID: NCT00347997 Withdrawn - Myopia Clinical Trials

A Study to Evaluate the Safety and Effectiveness of the 217z Laser With Zyoptix for Lasik

Start date: n/a
Phase: N/A
Study type: Interventional

A Study to demonstrate the safety and efficacy of wavefront laser refractive surgery treatments for myopia and astigmatism.

NCT ID: NCT00357981 Withdrawn - Dysmenorrhea Clinical Trials

Continuous Use of the Contraceptive Patch and the Personal Economic Impact.

Start date: n/a
Phase: N/A
Study type: Interventional

Dr. Eleanor Drey in the Department of Obstetrics, Gynecology and Reproductive Sciences UCSF is conducting a study to examine the personal and economic impact of continuous use of ORTHO EVRA, the contraceptive patch, on menstrual related symptoms for women who report having severe menstrual related symptoms.

NCT ID: NCT00358241 Withdrawn - Postoperative Pain Clinical Trials

Effects of Nerve Block on Knee Function After Knee Replacement

Start date: n/a
Phase: N/A
Study type: Interventional

Early physical therapy after knee surgery is very painful on top of pain from surgery. Pain following surgery can limit recovery. One way to treat pain is by giving intravenous (IV) pain medication with morphine. Another method is to use a "nerve block" which involves placing a thin catheter (tube) into the lower back near the nerves that sense pain in the knee and give a local anesthetic to numb the nerves. Sometimes both methods are used together. This research is being done to determine whether nerve blocks with a local anesthetic improve knee recovery in addition to providing pain relief as compared to IV pain medicine alone

NCT ID: NCT00360139 Withdrawn - Lipodystrophy Clinical Trials

Clinical Trial to Determine the Efficacy of Sculptra™ Dermal Filler for the Correction of Contour Deformities Caused by Lipoatrophy

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

Lipoatrophy is a condition that affects certain individuals, most commonly those who are infected with the HIV virus. Lipoatrophy however can also affect individuals who suffer from recurrent systemic infections, those who have a weakened immune system, or certain patients who suffer from cancer or receive chemotherapeutics. In contrast, lipoatrophy can sometimes be present in individuals who are perfectly healthy but have genetically predisposing factors that can contribute to facial emaciation or lipoatrophy. The function of injectable fillers for the treatment of dermal contour deformities is to smooth dermal depressions formed by the loss of volume. These often elastic contour fillers (also known as soft tissue augmentation devices) can correct hollowness around the eyes, add fullness to thin lips, balance a disproportionate face or correct topographical anomalies. This study aims to: - Objectively measure the improvement of contour-deformities after Sculptra™ injection from baseline to study closure by utilizing the Primos™ photographic/topographical measuring system. - Evaluate the efficacy, longevity and duration of volume-correction in subjects which are both HIV positive and HIV negative. - Assess the safety of Scupltra™ dermal filler when used to correct volume deformities caused by lipoatrophy in subjects that are HIV negative.

NCT ID: NCT00363441 Withdrawn - Clinical trials for Head and Neck Neoplasms

A Study of Conventional 3D Radiation vs. Intensity-Modulated Radiation in Squamous Cell Cancer of the Head and Neck

Start date: n/a
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized study of conventional 3d radiation versus intensity-modulated radiation in squamous cell cancer of the head and neck.

NCT ID: NCT00364897 Withdrawn - Primary ACL Tears Clinical Trials

Investigation of Clinical Outcome of ACL Reconstruction Utilizing Two Tibial Fixation Techniques, Concentric Tapered Interference Screws and Interference Screw and Sheath

Start date: n/a
Phase: Phase 2
Study type: Observational

Tibial fixation is the weak link when using soft tissue grafts and interference screws for fixation in a bony tunnel in ACL reconstruction. The Objective is to study two groups of patients undergoing double loop hamstring autograft ACL reconstruction and compare between the two tibial fixation devices: the tapered Deltascrew and the Intrafix screw and sheath .

NCT ID: NCT00365027 Withdrawn - Clinical trials for Ovarian Hyperstimulation Syndrome

Transfer of Fresh Versus Frozen/Thawed Embryos in IVF Cycles Where GnRH Agonist is Utilized for Oocyte Maturation.

Start date: n/a
Phase: N/A
Study type: Interventional

It has been suggested that in IVF cycles where GNRH agonist is utilized for final oocyte maturation in patients at risk of ovarian hyperstimulation, pregnancy rates are reduced. We hypothesize that the use of GNRH antagonist reduces pregnancy rates through an effect on the endometrium and not oocyte quality, therefore better results may be obtained by not returning these embryos in a fresh cycle but rather cryopreserving them and returning them to the uterus and a later stage.

NCT ID: NCT00367718 Withdrawn - Clinical trials for Nasopharyngeal Carcinoma

Trial of VELCADE in Patients With Metastatic or Locally Recurrent Nasopharyngeal Carcinoma

Start date: n/a
Phase: Phase 2
Study type: Interventional

This study seeks to test the Efficacy in terms of rates of disease response in metastatic nasopharyngeal carcinoma of the standard dose of velcade 1.3 mg/m2 given at the day 1,4,8,and 11 every 21 days schedule. The study uses a Simons 2 stage design and will enroll between 15-25 patients. Secondary endpoints studied include Pharmacokinetics, toxicities, EBV viral load and molecular characterization of EBV in plasma.