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NCT ID: NCT03836781 Completed - Clinical trials for Chronic Periodontitis

Teh Effect of Subgingival Irrigation Wif Ketorolac and Chlorhexidine in Patients Wif Chronic Periodontist

Start date: April 10, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

In this study, 40 patients with a history of Mild- Periodontitis who were diagnosed with clinical and radiographic findings showed that all of the periodontal parameters before the treatment, during the treatment period Then, scaling & Root planing and oral hygiene instructions were given to the patients, and after 2 weeks, the patients who received the study were randomly divided into two groups (Balanced Block Randomization) with four blocks according to the visit time. To group A, oral chlorohexidine and to B group, the drug Ketorolac was given. 5 mm of the drugs required every 15 days the areas underwent a gingival wash with an insulin syringe, which lasted for 3 months.

NCT ID: NCT03973775 Completed - Scabies Clinical Trials

A Bioequivalence Study With Clinical Endpoints to Evaluate the Safety and Therapeutic Equivalence of Permethrin Cream 5% & Elimiteā„¢ in Subjects With Scabies

Start date: April 10, 2018
Phase: Phase 3
Study type: Interventional

This phase III study was conducted to establish the clinical bioequivalence of Permethrin Cream 5% and Elimiteā„¢ in the treatment of scabies following a single application.

NCT ID: NCT04267770 Completed - Type 1 Diabetes Clinical Trials

Flat and Circadian Insulin Infusion Rates in Continuous Subcutaneous Insulin Infusion

FIRST1D
Start date: April 10, 2018
Phase: N/A
Study type: Interventional

Randomised controlled trial to contribute to the evidence base for the optimal initial insulin profile for adults with type 1 diabetes commencing insulin pump therapy.

NCT ID: NCT04436900 Completed - Clinical trials for Diabetes Mellitus, Type 2

Evaluation of Macular Structural and Functional Function Following Extensive Retinal Laser Therapy in Patients With Proliferative Diabetic Retinopathy

Start date: April 10, 2018
Phase: N/A
Study type: Interventional

The present study is a semi-experimental clinical trial that 20 patients (40 eyes) with PDR underwent PRP with ARC with a spot number of 1,200 to 1,500 per eye and spot size 500 micron with a duration of 200 ms. The variables of contrast sensitivity, macula thickness under fovea , BCVA, the width of thyroid under fovea , RNFL thickness in the four areas around the disc, and the quality of life questionnaire of all patients were recorded at the beginning of the study.Retinal and choroid under fovea thickness and RNFL thickness were assessed in four areas, one week and one month after the end of treatment, and all the variables mentioned earlier were evaluated three months after PRP surgery. This study is single group that the outcomes are compared before and after the intervention

NCT ID: NCT04464096 Completed - Clinical trials for Rheumatoid Arthritis

Can Musculoskeletal Ultrasound Predict Fall Risk in Rheumatoid Arthritis Patients?

Start date: April 10, 2018
Phase:
Study type: Observational

Rheumatoid patients have higher fall risk than normal population. Several fall risk factors were studied. No previous study investigated the role of musculoskeletal ultrasound as a predictor of fall risk in rheumatoid arthritis.

NCT ID: NCT04767724 Completed - Clinical trials for Carpal Tunnel Syndrome

Extracorporeal Shock Wave Versus Local Corticosteroid Injection for Carpal Tunnel Syndrome

Start date: April 10, 2018
Phase: Phase 4
Study type: Interventional

This RCT is to investigate the clinical effect of extracorporeal shock wave therapy (ESWT) compared to the local corticosteroid injection (LCI) in managing mild to moderate carpal tunnel syndrome (CTS).

NCT ID: NCT05015075 Completed - Bradycardia Clinical Trials

Cardiac Rehabilitation After Pacemaker Implantation

Start date: April 10, 2018
Phase: Phase 4
Study type: Interventional

The investigators assessed whether short-term cardiac rehabilitation following pacemaker implantation was enough to improve both physical function and quality of life.

NCT ID: NCT03162367 Completed - Burn Clinical Trials

Efficacy Of Autologous Epidermal Cell Suspension And Silver Sulfadiazine Ointment In Burn

Start date: April 10, 2019
Phase: Phase 2
Study type: Interventional

Different medical treatments are available for treatment of skin burns such as skin grafts and silver sulfadiazine ointment. These treatments are used for second degree burn as routine technique in burns units. Cell therapy is a new approach for treatment of skin disease.In this study we use autologous epidermal cell suspension to achieve better cosmetic and functional results in treatment of second degree burn.

NCT ID: NCT03445130 Completed - Anxiety Clinical Trials

A Study of the Effects of Lavender Aromatherapy on Preoperative Anxiety in Breast Surgery Patients

Start date: April 10, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of lavender aromatherapy on preoperative anxiety by measuring changes in pulse rate and anxiety core using Spielberger State-Trait Anxiety Index questionnaires and on postoperative pain medicine usage. Study participants will then be randomized into one of four groups; either they will receive 2 drops of lavender (Lavandula Angustifolia) oil (LO) or 2 drops of Michelia Alba Leaf oil (MA) or 2 drops of unscented Almond oil (AO) or two drops water on the inside of an oxygen face mask for 15 minutes. Linalool makes up ~30% of Lavandula Angustifolia oil and is believed to be its most active anti-anxiety component. Before and after treatment, anxiety level will be measured using the Spielberger State-Trait Anxiety Inventory.

NCT ID: NCT03506438 Completed - Critical Illness Clinical Trials

Addressing Palliative Care Needs Among Intensive Care Unit Family Members

ICUconnect
Start date: April 10, 2019
Phase: N/A
Study type: Interventional

The quality of palliative care is highly variable for many patients treated in intensive care units (ICUs) and their family members. To address these challenges, the investigators will test the impact of a mobile app designed to help families navigate ICU-based palliative care vs. usual care. The investigators hypothesize that the intervention will reduce patient/family member unmet palliative care needs and improve the quality of clinical-family communication in racially/ethnically diverse populations.