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NCT ID: NCT01973101 Recruiting - Clinical trials for Patients Diagnosed With Advanced Carcinoma of Uterine Cervix t

Non-comparative Study of Treatment With Induction Chemotherapy With Cisplatin and Gemcitabine Followed by Chemoradiation or Definitive Chemoradiation in Invasive Locally Advanced Carcinomas of Uterine Cervix.

CIRCE
Start date: June 2012
Phase: Phase 2
Study type: Interventional

The purpose of this phase II study is to determine the survival free disease of patients diagnosed with invasive locally advanced carcinomas of uterine cervix treated with induction chemotherapy with cisplatin and gemcitabine followed by chemoradiation and definitive chemoradiation.

NCT ID: NCT01972607 Completed - Clinical trials for Headache Disorders, Primary

The Effect of Aerobic Exercise Training for Migraine Prevention.

Start date: March 2012
Phase: N/A
Study type: Interventional

This study has been designed in order to know the effect of 12 weeks of aerobic exercise training for migraine prevention. We hypothesized that the exercise training could reduce the number of days with migraine and the number of attacks per month in the treated group.

NCT ID: NCT01972568 Completed - Clinical trials for Lupus Erythematosus, Systemic

Efficacy and Safety of Atacicept in Systemic Lupus Erythematosus

ADDRESS II
Start date: December 2013
Phase: Phase 2
Study type: Interventional

This is a multi-center, double-blind, randomized, Phase 2b trial to evaluate the efficacy of atacicept in subjects with systemic lupus erythematosus (SLE).

NCT ID: NCT01972529 Completed - Clinical trials for Thrombocytopenia Associated With Liver Disease

Treatment of Thrombocytopenia in Patients With Chronic Liver DiseaseUndergoing an Elective Procedure

Start date: February 2014
Phase: Phase 3
Study type: Interventional

This is a global, multicenter, randomized, double-blind, placebo-controlled, parallel group study using avatrombopag to treat adults with thrombocytopenia associated with liver disease. The study will evaluate avatrombopag in the treatment of thrombocytopenia associated with liver disease prior to an elective procedure to reduce the need for platelet transfusions or any rescue procedure for bleeding due to procedural and post-procedural bleeding complications. Participants will be enrolled into 2 cohorts according to mean baseline platelet count and, within each baseline platelet count cohort will be further stratified by risk of bleeding associated with the elective procedure (low, moderate, or high) and hepatocellular carcinoma (HCC) status (Yes or No).

NCT ID: NCT01972412 Unknown status - Diabetes Mellitus Clinical Trials

Telephone Use for Care of Persons With Diabetes Mellitus.

TCDM
Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether phone use contributes to diabetes control.

NCT ID: NCT01972100 Completed - Healthy Clinical Trials

Use of Low-level Laser Therapy (808nm) to Muscle Fatigue Resistance

Start date: April 2013
Phase: N/A
Study type: Interventional

The study hypothesis is a improved muscle fatigue resistance induced by low-level laser therapy applied between sets of intense exercises.

NCT ID: NCT01971983 Active, not recruiting - Low Back Pain Clinical Trials

Effect of Two Osteopathic Techniques on Thickness of Paravertebral Muscles of the Lumbar Spine

Start date: February 2013
Phase: N/A
Study type: Interventional

The objective of this randomized controlled trial is to describe the effect of two osteopathic techniques - "high velocity, low amplitude" (HVLA) and muscle energy (ME) - on thickness, activation, strength, pressure pain threshold (PPT) of the paravertebral muscles at the lumbar spine, as well as the peak plantar pressures immediately and after a two-day follow-up. The muscle thickness of the paravertebral muscles at the lumbar spine, namely internal oblique, external oblique and transversus abdominis can be altered after the application of 'high-velocity low-amplitude'(HVLA)and 'muscle energy' (ME)techniques immediately and after a two-day follow-up.

NCT ID: NCT01971099 Completed - Clinical trials for Hypoactive Sexual Desire Disfunction

Effects of Tribulus Terrestris in Women With Hypoactive Sexual Desire Disorder

Start date: May 2013
Phase: Phase 4
Study type: Interventional

Hypoactive Sexual Desire Disorder (HSDD) is the most prevalent female sexual dysfunction in society and is strongly linked to the quality of life of women. The androgen hormones decline over age in the premenopausal period, which occurs around 20 years. Tribulus terrestris is a plant native to India, recommended in the treatment of infertility, low libido and impotence. Its main active ingredient is the protodioscin, which has been attributed to an increase in testosterone levels and improved sexual function. The aim of this study is to evaluate the effects of Tribulus Terrestris in premenopausal women with HSDD.

NCT ID: NCT01971034 Completed - Clinical trials for Pancreatic Adenocarcinoma Advanced or Metastatic

Treatment of Patients With Advanced Pancreatic Cancer After Gemcitabine Failure.

Start date: June 2011
Phase: Phase 2
Study type: Interventional

In Brazil pancreatic adenocarcinoma represents 2% of tumors, and 4% mortality being an uncommon disease, however very aggressive.Only 20% of cases are indicated for curative surgery, of which only 20% are alive within 5 years. For locally, advanced or metastatic disease, since 1997, single chemotherapy with gemcitabine is the standard treatment for first line, with survival around 6 months approximately.There is no standard treatment regimen for second-line, however Paclitaxel demonstrated effect on second-line phase II study. Metformin is an oral hypoglycemic drug used for treatment of diabetes mellitus. There is a growing number of preclinical studies which show antitumor effect against pancreatic adenocarcinoma, probably due to the effect of anti-insulin growth factor (IGF-1). This study will add metformin to standard treatment for second line of locally advanced or metastatic pancreatic adenocarcinoma in ICESP previously treated with gemcitabine. The objective is to evaluate whether metformin improves the efficacy of the standard treatment with paclitaxel by clinical and radiological evaluation.

NCT ID: NCT01969383 Recruiting - Clinical trials for Healthy Individuals.

Comparative Analysis Between Electrical Muscle Activity In Water And Soil

Start date: April 2013
Phase: N/A
Study type: Interventional

Muscle activity in the aquatic environment was investigated while performing different exercises by electromyography analysis, due to conflicting results in the literature in relation to the floor. This study evaluated and compared the electrical activity of the rectus femoris and biceps femoris, in aquatic method and on the floor, during flexion and knee extension exercises with and without load.