Clinical Trials Logo

Signs and Symptoms clinical trials

View clinical trials related to Signs and Symptoms.

Filter by:

NCT ID: NCT02157675 Completed - Clinical trials for Delayed Onset Muscle Soreness

Effects of a Polyherbal Supplement on the Signs and Symptoms of Delayed Onset Muscle Soreness

Start date: April 2014
Phase: Phase 4
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled, crossover design study in healthy subjects to determine the effects of a polyherbal supplement on the signs and symptoms of delayed onset muscle soreness (DOMS) induced by eccentric exercise of the arm.

NCT ID: NCT02125253 Completed - Clinical trials for Seasonal Allergic Rhinitis

Study to Compare the Therapeutic Equivalence of Mometasone Furoate Nasal Spray, 50 mcg With Nasonex Nasal Spray in the Relief of the Signs and Symptoms of Seasonal Allergic Rhinitis

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

To evaluate the therapeutic equivalence of the lest formulation of Mometasone Furoate Nasal Spray, 50 mcg to the marketed formulation NASONEX® (mometasone furoate monohydrate) Nasal Spray, 50 mcg/actuation in patients with seasonal allergic rhinitis

NCT ID: NCT02109185 Completed - Clinical trials for Treatment of the Signs and Symptoms of Seasonal Allergic Rhinitis

A Comparison of Mometasone Nasal Spray, Nasonex Nasal Spray, Nasonex Nasal Spray Suspension, & Placebo for Treatment of Seasonal Allergies for Safety, Efficacy, & Superiority in 1520 Male & Female Volunteers

Start date: September 2013
Phase: Phase 1
Study type: Interventional

The study will compare the safety and efficacy of a generic mometasone nasal spray to the reference listed drugs in the treatment of seasonal allergic rhinitis. Additionally both the test and the reference formulations will be tested for superiority against a placebo nasal spray.

NCT ID: NCT02075320 Completed - Signs and Symptoms Clinical Trials

Evaluation of the Lung Nodule Sensitivity of Stationary Chest Tomosynthesis in Patients With Known Lung Nodules

Start date: February 2014
Phase: N/A
Study type: Interventional

Purpose: The proposed research, if successfully implemented, will result in a low-dose, low-cost, and highly effective method for screening of lung cancer, leading to reduction of the lung cancer mortality rate. Using the stationary Digital Chest Tomosynthesis (s-DCT) system the imaging dose for a full tomosynthesis scan is expected to be only 10% of that from a low-dose computed tomography (CT). The targeted imaging time of 2s is 1/5 to 1/3 of that from a current commercial digital chest tomosynthesis (DCT) system at the same imaging dose. Beyond lung cancer screening, the low-dose and sensitive 3D lung imaging modality will likely to find applications in areas such as monitoring of pediatric cystic fibrosis patients where reduction of imaging dose is critical. Participants: One hundred (100) patients undergoing a clinical non-contrast CT for their lung nodules will be asked to have this procedure (scan) within 2 weeks (+/- 1 week) of their clinical CT and chest radiograph, with no intervening procedures or therapies. Procedures (methods): The purpose and endpoint of this study is to compare the sensitivity of the s-DCT system to the conventional chest radiographs with non-contrast chest CT as the reference standard. One hundred (100) patients undergoing a clinical non-contrast CT for their lung nodules will be asked to have this procedure (scan) within 2 weeks (+/- 1 week) of their clinical CT and chest radiograph, with no intervening procedures or therapies.

NCT ID: NCT02012127 Completed - Acromegaly Clinical Trials

Description of Sign-and-symptom Associations at Acromegaly Diagnosis.

ACRO-POLIS
Start date: September 2013
Phase:
Study type: Observational

The purpose of this study is to describe most characteristic association of signs and symptoms present at the time of acromegaly diagnosis.

NCT ID: NCT01954199 Completed - Low Back Pain Clinical Trials

The Effectiveness of Neurodynamic Techniques in Patients With Nerve-Related Leg Pain

Start date: March 2015
Phase: N/A
Study type: Interventional

This study aims to verify if patients with nerve-related leg pain benefits from neurodynamic treatment over two weeks.

NCT ID: NCT01872663 Completed - Clinical trials for Respiratory Tract Diseases

Influence of Different Physical Therapy Resources Application After Reduction Stomach Surgery

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

The aim of this study will be to investigate the effects of using physical therapy resources in the postoperative morbidly obese individuals undergoing gastroplasty. It is believed that the application of these various features of physiotherapy after abdominal surgery may contribute differently in restoring lung function and prevention of pulmonary complications and can thus identify the resources that can contribute more effectively in post-operative bariatric surgery.

NCT ID: NCT01824511 Completed - Smoking Clinical Trials

Effects of Quitting Study A Test of Pre-clinical Findings

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

The most widely-accepted animal model of nicotine withdrawal states stopping nicotine makes rewarding events become less rewarding. The current study will test if this is true in humans. If we find tobacco abstinence does make rewards less rewarding, this would suggest new symptoms to add to official descriptions of nicotine withdrawal. It would also suggest we need to develop new behavioral and pharmacological interventions to correct this problem. If stopping smoking does not make rewards less rewarding, this would suggest this animal model does not apply to the human condition and we need to continue to search for an animal model of tobacco withdrawal that is relevant to smokers stopping smoking.

NCT ID: NCT01796925 Completed - Clinical trials for Sleep Apnea, Obstructive

Targeted Hypoglossal Neurostimulation Study #2

THN2
Start date: February 2013
Phase: N/A
Study type: Interventional

The objective of the study is to confirm the safety and efficacy in patients utilizing the aura6000 System for the treatment of Obstructive Sleep Apnea (OSA).

NCT ID: NCT01786681 Completed - Clinical trials for Respiratory Tract Diseases

Use of Positive Pressure in Morbidly Obese Patients Undergoing Reduction Stomach Surgery

Start date: August 2011
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effects of using positive pressure in the preoperative, intraoperative and postoperative morbidly obese individuals undergoing gastroplasty. It is believed that the application of these devices before, during or after surgery can help to improve the lungs and reduce pulmonary complications after surgery to reduce the stomach.