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NCT ID: NCT00944268 Not yet recruiting - Anxiety Clinical Trials

Efficacy and Tolerability Study to Treat Mild and Moderate Anxiety

E01ATCAL0308
Start date: September 2009
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and tolerability of the combination use of Passiflora incarnata L, Crataegus oxyacantha and Salix alba L in mild and moderate anxiety. Clinical study phase III, multicenter, prospective, open. Patients will be included in sufficient quantity to achieve the minimum number of 124 evaluable patients.

NCT ID: NCT00926419 Not yet recruiting - Varicella Clinical Trials

Serological Evaluation of Varicella and Hepatitis A Vaccines Using Injector Delivery

InjHepAVar
Start date: June 2009
Phase: Phase 2/Phase 3
Study type: Interventional

This study aims to assess immunogenicity and safety of nd influence of the delivery system (needle-free injector or syringe with needle) of fractional doses (dose sparing) of two vaccines (Varicella and Hepatitis A vaccines) in children aged 13 to 30 months.

NCT ID: NCT00925639 Not yet recruiting - Menopause Clinical Trials

Effects of the Concentrated Extract of Soy on Coagulation Factors After Menopause

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

Hypoestrogenism, common in menopause, is responsible for systemic and metabolic changes affecting women's wellness, favoring hot flashes, urogenital atrophy and bone mass loss. Hormone reposition therapy (HRT) with estrogen or estrogen associated to progesterone is administered to minimize these effects. Meanwhile, the beneficial effects of HRT are known, there is still concern about its adverse effects such as thromboembolic and cardiovascular effects, increased risk of breast and endometrial cancer. Thus, there is an increasing interest in the development of phytohormonal HRT. The aim of the investigators' study is to evaluate the effects of concentrated extract of soy on hypercoagulation markers in menopausal women.

NCT ID: NCT00889356 Not yet recruiting - Bacterial Vaginosis Clinical Trials

Evaluate Efficacy, Tolerability & Safety of Combination of Clindamycin and Ketoconazole for the Treatment of Mixed-Type Vaginosis, Bacterial Vaginosis and Candidiasis

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the Efficacy, Tolerability & Safety of Combination of Clindamycin 100mg and Ketoconazole 400mg in Vaginal Capsules, used for 7 consecutive days in patients with Mixed-Type Vaginosis compared to Combination of Tetracycline 100mg and Amphotericin B 50mg in Vaginal Cream.

NCT ID: NCT00877409 Not yet recruiting - Acne Vulgaris Clinical Trials

Safety and Efficacy Study of Acnase Creme in the Treatment of Acne Vulgaris I and II

ACNASE
Start date: April 2009
Phase: Phase 3
Study type: Interventional

The objective of this study is to establish the safety in use of the topical drug Acnase Creme and its effectiveness in treatment of acne grade I (comedones) and II (comedones, papules, pustules).

NCT ID: NCT00757458 Not yet recruiting - Drug Contamination Clinical Trials

Evaluation of Bacterial and Fungal Contamination During Propofol Continuous Infusion

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

The purpose of this study is to verify the existence of bacterial and/or fungal contamination during different technics of propofol with or without EDTA continuous infusion in patients undergoing general anesthesia.

NCT ID: NCT00661063 Not yet recruiting - Pain Clinical Trials

Diabetic Neuropathy Topical Treatment

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

Comparative study of efficacy and safety of ketamine, clonidine, mixture of both and placebo in patients with diabetic neuropathic pain

NCT ID: NCT00616044 Not yet recruiting - Hip Fractures Clinical Trials

Continuous Spinal Anesthesia Versus Combined Spinal Epidural Block

Spinocath
Start date: March 2008
Phase: N/A
Study type: Interventional

In major orthopaedic surgery of the lower extremities both continuous spinal anesthesia (CSA) and combined spinal epidural anesthesia (CSE) are safe and reliable anaesthesia methods. Our results suggest that both continuous spinal anesthesia and combined spinal epidural anesthesia provide good surgical conditions with a low incidence of complications. The sensory block level and hemodynamic changes were lesser with CSA.

NCT ID: NCT00385983 Not yet recruiting - Thyroid Nodule Clinical Trials

Total Thyroidectomy With Harmonic Scalpel®

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

Harmonic scalpel is a new surgical instrument. Its use has been recommended in patients submitted to total thyroidectomy. Few randomized controlled trials has been published. However they had small sample sizes, used intermediate outcomes and included different surgical procedures. Our objective is to asses the use of Harmonic scalpel in patients submitted to total thyroidectomy using surgical complications, operative time, drainage volume, postoperative pain, length of stay and costs as outcomes. Our hypothesis is that Harmonic scalpel decreases operative time,drainage volume, postoperative pain, length of stay and costs without increasing surgical complications

NCT ID: NCT00334477 Not yet recruiting - Clinical trials for Erectile Dysfunction

Efficacy and Safety of Tadalafil in Hemodialysis Patients

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

The purpose of this study is to check the safety and efficacy of a pde5 inhibitor, tadalafil, is a special group of patients: Renal chronic patients in hemodialysis treatment.