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NCT ID: NCT03761771 Completed - Clinical trials for Sensitivity of the ADS in Identifying Polyps in Real-world Colonoscopy

Artificial Intelligence Identifying Polyps in Real-world Colonoscopy

Start date: November 1, 2018
Phase:
Study type: Observational

Recently, artificial intelligence (AI) assisted image recognition has made remarkable breakthroughs in various medical fields with the developing of deep learning and conventional neural networks (CNNs). However, all current AI assisted-diagnosis systems (ADSs) were established and validated on endoscopic images or selected videos, while its actual assisted-diagnosis performance in real-world colonoscopy is up to now unknown. Therefore, we validated the performance of an ADS in real-world colonoscopy, which is based on deep learning algorithm and CNNs, trained and tested in multicenter datasets of 20 endoscopy centers.

NCT ID: NCT03761719 Completed - Clinical trials for Older People With Diabetes Mellitus

The Influence of HDL Function on Cognitive Function

Start date: July 30, 2018
Phase:
Study type: Observational

Older people with diabetes mellitus are at risk of cognitive decline and dementia. We therefore propose to examine the potential influence of HDL function on global cognitive function and brain structures in older people with DM.

NCT ID: NCT03761368 Completed - Clinical trials for Remote Ischemic Preconditioning

Remote Ischemic Preconditioning and Contrast Induced - Acute Kidney Injury in Patients Undergoing Elective PCI

Start date: March 1, 2015
Phase: N/A
Study type: Interventional

Prospective, randomized, sham-controlled clinical study was conducted to assess whether RIPC reduces the incidence of CI-AKI measured standard way of using SCr concentration but also with the use of serum NGAL as a new potential biomarker of kidney injury. Furthermore, the aim of investigation was to analyse the safety and clinical outcomes of RIPC after elective coronary angiography (CA) followed by percutaneous coronary intervention (PCI).

NCT ID: NCT03761225 Completed - Clinical trials for Metastatic Castrate Resistant Prostate Cancer

Masitinib Plus Docetaxel in Metastatic Castration-resistant Prostate Cancer

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

Study of masitinib plus docetaxel as first-line chemotherapy in men with metastatic castration-resistant prostate cancer.

NCT ID: NCT03760809 Completed - Clinical trials for Agitated; State, Acute Reaction to Stress

Dexmedetomidine Combined With Hydromorphone in Tonsillectomy and Adenoidectomy

Start date: January 4, 2019
Phase: Phase 4
Study type: Interventional

Tonsillectomy and adenoidectomy is one of the most common pediatric surgeries, and agitation and severe postoperative pain have been considered a very common complications. Dexmedetomidine mainly inhibits the release of norepinephrine by acting on the α-adrenergic receptor of the brainstem nucleus, which can produce good sedative effects. Hydromorphone has a longer duration of action than fentanyl, and it also has a certain sedative effect. The combination of the two is more conducive to the management of postanesthetic agitation and pain. This study was to compare the effect of different doses of dexmedetomidine combined with hydromorphone in the sedation and analgesia after pediatric tonsillectomy and adenoidectomy.

NCT ID: NCT03760627 Completed - Clinical trials for Mental Health Wellness 1

Evaluation of A Mindfulness Resiliency Training Program for Refugees Living in Jordan

Start date: November 30, 2018
Phase: N/A
Study type: Interventional

To estimate the efficacy of a structured, scalable and replicable psychosocial intervention targeting refugees living in Jordan, Amman who have been forced to flee their homes due to regional conflicts.

NCT ID: NCT03760601 Completed - Clinical trials for Intrusive Memories of Trauma, Symptom of Post Traumatic Stress Disorder (Criterion B1)

A Brief Cognitive Intervention After Intrusive Memories of Trauma With Young Refugees: An Extension

Start date: March 25, 2019
Phase: N/A
Study type: Interventional

This research study is designed to investigate the use of a simple cognitive task (a memory cue and 10 minute time gap, followed by playing the computer game "Tetris") for decreasing the number of intrusive memories of trauma among young refugees and asylum seekers. The design is a single case experimental AB design with optional replication (ABAB). Participants will aim to complete a no-intervention phase ('A': baseline phase) of one week followed by a one-week intervention phase ('B'), including a one-session intervention with a researcher comprising the simple cognitive task, followed by instructions to continue to use the technique self-guided in the subsequent week. Follow ups are conducted after each week to monitor the occurrence of intrusive memories of trauma in a pen-and-paper diary. It is predicted that participants will report fewer intrusive memories during the intervention phase than during the preceding baseline phase.

NCT ID: NCT03760510 Completed - Clinical trials for Mechanical Ventilation Complication

Endotracheal Tube Securement Study

ETTS
Start date: May 17, 2017
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of endotracheal tube securement techniques, a pragmatic, randomized controlled trial will compare the effect of adhesive tape versus endotracheal tube fastener on complications including lip ulcers, facial skin tears, endotracheal tube dislodgement, and ventilator associated pneumonia among critically ill adults requiring intubation and mechanical ventilation for at least 24 hours.

NCT ID: NCT03760198 Completed - Clinical trials for Hyperhidrosis Primary Focal Axilla

Evaluate the Efficacy and Safety of MEDITOXIN in Treatment of Primary Axillary Hyperhidrosis

Start date: August 3, 2018
Phase: Phase 3
Study type: Interventional

This study is intented to evaluate the efficacy and safety of MEDITOXIN compared to placebo in treatment of primary axillary hyperhidrosis.

NCT ID: NCT03760185 Completed - Clinical trials for Intraoperative Floppy Iris Syndrome

Pupil Dilation for Treatment of IFIS

Start date: January 4, 2019
Phase: Phase 2
Study type: Interventional

A novel intervention for targeting the treatment of Intraoperative Floppy Iris Syndrome.