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NCT ID: NCT03790150 Completed - Clinical trials for Mechanical Ventilation Complication

National Approach to Standardize and Improve Mechanical Ventilation

NASAM
Start date: January 1, 2019
Phase:
Study type: Observational

This is a pre-post implementation cohort study. This is a data driven quality improvement project which aims to improve the care of mechanically ventilated patients through the implementation of a bundle of evidence based practices, with a goal of reducing ventilator associated events and mortality.

NCT ID: NCT03789812 Recruiting - Oral Hygiene Clinical Trials

Oral Hygiene in Patients With Orthodontic Fixed Appliances

Start date: December 3, 2018
Phase: N/A
Study type: Interventional

The study aims to compare the efficacy of the use of different methods of teeth cleaning on the oral hygiene in patients with orthodontic fixed appliance

NCT ID: NCT03788135 Completed - Healthy Clinical Trials

Localized Muscle Cooling on Balance in Healthy Individuals

Start date: January 5, 2019
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of localized muscle cooling on static and dynamic stability in healthy adults.

NCT ID: NCT03787914 Completed - Tuberculosis Clinical Trials

Effect of Community Mobile Outreach Approach Compared to Facility Based Directly Observed Treatment Short Course on Treatment Outcome Among Tuberculosis Patients in Jeddah: A Randomized Controlled Trial

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

To compare the effectiveness of the community mobile outreach approach in improving treatment outcomes (success rate) among tuberculosis patients with those being treated with facility based directly observed treatment short course (DOTS) in Jeddah region.

NCT ID: NCT03785522 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Research Study, Looking at How Tresiba® Works in People With Type 2 Diabetes in Local Clinical Practice in Saudi Arabia

UPDATES
Start date: December 23, 2018
Phase:
Study type: Observational

The purpose of the study is to collect information on how Tresiba® works in real world patients. Patients will get Tresiba® as prescribed to them by their study doctor. The study will last for about 6 to 8 months. Patients will be asked questions about their health and diabetes treatment as part of their normal study doctor's appointment.

NCT ID: NCT03782714 Completed - Pulpotomy Clinical Trials

Low-level Laser Therapy Versus Formocresol in Primary Molar Pulpotomies

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

This study aimed to assess and compare the clinical and radiographic success rates of LLLT and FC for pulpotomy in human primary teeth. One hundred and six primary molars from 36 children aging five to eight years were included and randomly assigned into two equal groups; LLLT group and FC group. Teeth were evaluated clinically and radiographically at 3, 6 and 12 months.

NCT ID: NCT03779698 Completed - Dental Caries Clinical Trials

BiodentineTM Versus Formocresol Pulpotomy Technique in Primary Molars

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

The objective of this clinical study was to prospectively compare the clinical and radiographic success rates of BiodentineTM pulpotomies versus formocresol pulpotomies in children vital primary molars. A randomized, split-mouth study design was used with a sample of 37 healthy children aged 4- to 8-year-old. A total of 56 pairs (112 teeth) of carious primary teeth, 1 pair per child, were selected for treatment. One tooth from each pair was randomly assigned to either the BiodentineTM pulpotomy group or the formocresol pulpotomy group. Children were followed-up at 3, 6 and 12 months for clinical evaluation and at 6 and 12 months for radiographic evaluation. Data were collected, tabulated and analyzed using Fisher exact and McNemar tests. The level of significance was set at P < 0.05.

NCT ID: NCT03779581 Completed - Clinical trials for Scoliosis Idiopathic

Self Correction Exercises for Idiopathic Scoliosis Among Adolescents. A Randomised Controlled Trial

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Adolescent idiopathic scoliosis (AIS) is a three-dimensional spinal deformity with an unknown cause that affects adolescents aged 10 or older. A standing posterior-anterior radiograph with a Cobb angle greater than 10 degrees is used to make the diagnosis. Depending on the severity of the spinal deformity, conservative treatments and surgery are used to treat AIS. Patients whose spinal curvature is greater than 45 degrees are typically considered for surgery. The majority of patients with AIS receive conservative treatments to prevent and slow the progression of the curve. 2 Orthotic intervention (OI) and scoliosis-specific exercise (SSE) are commonly recommended by the International Society on Scoliosis Orthopaedic and Rehabilitation Treatment for patients with a curvature between 20 and 45 degrees. Self correction exercises are the group of spinal extension, lateral spinal flexion and rotational exercises performed to correct spinal deviation. Exercises are performed in a different fundamental postures.

NCT ID: NCT03778697 Completed - Obesity, Childhood Clinical Trials

Endosleeve in Adolescents

Start date: December 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

In this study, the investigators assess the safety and efficacy of endoscopic sleeve gastroplasty in adolescents with obesity.

NCT ID: NCT03778099 Completed - Clinical trials for Polycystic Ovary Syndrome

The Effect of Cinnamon on Ovulation Induction in Women With Polycystic Ovary Syndrome

PCOS
Start date: September 20, 2018
Phase: Phase 3
Study type: Interventional

Title: The effect of cinnamon supplementation on ovulation induction in women with polycystic ovary syndrome, Jeddah 2019: Randomized Double-Blind Placebo-controlled trial Phase: III Population: 118 women with polycystic ovary syndrome will be recruited from Obstetrics and Gynecology clinics in King Abdul-Aziz University Hospital, Jeddah 2019. Subject Participation Duration: Each participant will be followed for three months. Intervention: 2g of cinnamon capsules daily will be provided. Objectives: Primary Objective: 1. To compare the effectiveness of cinnamon supplement in combination with clomiphene citrate versus clomiphene citrate alone on ovulation in women with PCOS, in King Abdul-Aziz University Hospital in Jeddah 2019. 2. To measure the difference in insulin resistance after three months of cinnamon supplementation in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019. 3. To determine the effect of cinnamon and CC on menstrual cyclicity, approximated by menstrual frequency, during the study period, in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019 4. To evaluate the quality of life in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019. Secondary Objectives: - To measure the pregnancy rate in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019 Description of Study Design: The participants will be randomized in 1:1 fashion. Allocation concealment will be ensured using similar bottles labeled by letters A and B, to receive either the combination of cinnamon supplement and clomiphene citrate or clomiphene citrate with placebo. First visit: Patients will be evaluated during the early follicular phase for progesterone level and HOMA-IR and QUICK-I. Follow up: 3 months. Last Visit: Patients will be re-evaluated to compare the difference.