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Signs and Symptoms clinical trials

View clinical trials related to Signs and Symptoms.

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NCT ID: NCT03994809 Completed - Pain Clinical Trials

International Study of Biofield Therapy

Start date: January 1, 2008
Phase:
Study type: Observational

Participants from 14 different countries received a single session of biofield therapy (Okada Purifying Therapy) lasting 30 minutes or longer from the volunteer practitioners. Before and after the therapy, they reported the severity of physical pain, anxiety/depression, dizziness/palpitation, and overall symptoms. The team compared the effectiveness/safety of biofield therapy between countries and analyzed the factors associated with the outcomes.

NCT ID: NCT03972605 Completed - Clinical trials for Benign Breast Findings

Delphinus SoftVue™ ROC Reader Study

DMT SV RRS2
Start date: June 8, 2019
Phase:
Study type: Observational

The purpose of this multi‐reader, multi‐case (MRMC) reader study is to evaluate reader performance when SoftVue™ automated breast ultrasound and screening mammography are combined, compared to screening mammography alone, in women with dense breast parenchyma. This reader study will include approximately 32 radiologist readers and a sample of approximately 200 breast screening cases to be selected from the library of images collected under Delphinus Protocol #DMT‐2015.001 (NCT03257839) Arm 1 Phases B, C, and D. The reader study image case set will be enriched with cancer cases.

NCT ID: NCT03939000 Completed - Clinical trials for Type 2 Diabetes Mellitus

Clinical Profile and Laboratory Finding of DFU From Tertiary Hospitals in Bali

Start date: March 2016
Phase:
Study type: Observational

The investigators want to obtain the clinical profile, hematological profile, and biochemical profile from diabetic foot ulcer (DFU) patient.

NCT ID: NCT03898570 Completed - Clinical trials for Cardiovascular Diseases

Distributed Registry

Start date: April 1, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to test if a patient can be directly connected to a quality assurance (QA) database, traditionally known as a registry. Patient-reported outcomes (PRO) data will be entered into the database directly from a patient's mobile phone from their index procedure for 12 months. The investigators hope this study to be a "proof of concept" for such a distributed registry and evaluate 1) consistency of data acquisition, 2) engagement of patients, 3) overall value of patient-reported outcomes to enhance long term follow up.

NCT ID: NCT03713359 Completed - Signs and Symptoms Clinical Trials

Clinical Trial for Measles - Rubella Combined Vaccine (MRVAC) Produced by POLYVAC (Phase III)

Start date: April 2016
Phase: Phase 3
Study type: Interventional

The study is conducted to evaluate the safety and Immunogenicity of Measles-Rubella combined vaccine MRVAC produced by POLYVAC (phase 3) on Vietnamese volunteers and to demonstrate non-inferiority on the immunogenicity of MRVAC in comparison to MR vaccine produced by Serum Institute, India.

NCT ID: NCT03608735 Completed - Clinical trials for Functional Gastrointestinal Disorders

Prevalence of Functional Gastrointestinal Disorders (FGIDs), Related Signs and Symptoms in Infants/Toddlers in Thailand

GI_Planet
Start date: November 7, 2018
Phase:
Study type: Observational

Prevalence and impact of Functional Gastrointestinal Disorders (FGIDs) and Related Signs and Symptoms in Infants and Toddlers in Thailand

NCT ID: NCT03544268 Completed - Signs and Symptoms Clinical Trials

Academic-Industrial Partnership for Translation of Acoustic Angiography

Start date: March 25, 2019
Phase: Phase 4
Study type: Interventional

Purpose: The primary objective of this single arm study is to compare the sensitivity and specificity of acoustic angiography with traditional b-mode ultrasound in the distinction of malignant versus benign breast lesions. Secondary objectives include a comparison of area under the curve (AUC) for acoustic angiography versus b-mode ultrasound, and comparison of radiologist preference for the two imaging techniques for each of 3 lesion characteristics. Participants: Sixty patients who are to have a clinical surgical breast biopsy based on results from pre-study standard of care (SOC) imaging will be recruited from the UNC Breast Clinic for participation in the study. Procedures (methods): This is a one arm single center study of patients with suspicious breast lesions (BIRADS 4 or 5) from the UNC Breast Clinic that consent to undergo an acoustic angiography in conjunction with b-mode ultrasound prior to their scheduled biopsy.

NCT ID: NCT03543709 Completed - Fibromyalgia Clinical Trials

Evaluation of Fibromyalgia With Disease Activity and Clinical Findings in Women With Behçet's Disease

Start date: June 11, 2018
Phase:
Study type: Observational [Patient Registry]

In the literature, the relationship between fibromyalgia and disease activity has been assessed in a few studies without discrimination between women and men.In this study, it was aimed to evaluate the relationship between fibromyalgia and disease activity in women with Behçet's disease.

NCT ID: NCT03471923 Completed - Clinical trials for Nervous System Diseases

Non-Motor Features of Cervical Dystonia (CD)

Start date: March 26, 2018
Phase:
Study type: Observational

This study will examine the prevalence of four previously identified non-motor markers in a population of cervical dystonia patients, unaffected family members, and healthy volunteers in an attempt to identify a distinct combination of non-motor symptoms that may be indicative of disease development.

NCT ID: NCT03451396 Completed - Dry Eye Clinical Trials

Effect of Lifitegrast on Dry Eye Disease Signs and Symptoms

Lifitegrast
Start date: December 12, 2016
Phase: Phase 4
Study type: Interventional

To determine whether a fall in tear osmolarity precedes improvement in symptoms and signs of dry eye in dry eye patients treated topically with 5% lifitegrast drops for 3 months.