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NCT ID: NCT03801252 Completed - Obesity Clinical Trials

Antibiotic Prophylaxis to Prevent Obesity-Related Induction Complications in Nulliparae at Term

APPOINT
Start date: December 12, 2018
Phase: Early Phase 1
Study type: Interventional

Obesity increases the risk of pregnancy complications, including among others puerperal infections and cesarean delivery, and risk rises with increasing body mass index (BMI). Class III obesity is an indication for delivery by 39 weeks, and these patients have a high rate of labor induction. In nulliparous women from the general population (obese and non-obese), labor induction at 39 weeks (compared to expectant management) is associated with less morbidity and a lower cesarean rate. Antibiotic prophylaxis, standard before cesarean delivery, is associated with less post-cesarean infection if azithromycin is added to the standard cefazolin. In this placebo-controlled pilot trial, investigators will estimate the parameters necessary to calculate the sample size for a planned multicenter clinical trial of prophylactic antibiotics administered at the start of labor inductions of morbidly obese nulliparous women at term.

NCT ID: NCT03801226 Completed - Volume Overload Clinical Trials

Zero Sodium Peritoneal Dialysate Protocol Pilot Study

Start date: December 1, 2018
Phase: Early Phase 1
Study type: Interventional

The following pilot study will be undertaken to determine the effects of use of a zero-sodium peritoneal dialysate solution (10% dextrose in sterile water) on sodium removal as compared to a standard peritoneal dialysis solution.

NCT ID: NCT03801213 Completed - Clinical trials for Urinary Tract Infection Bacterial

Evaluation of Urine Samples Obtained by Bladder Stimulation for the Diagnosis of Urinary Tract Infection in Infants

EEStiVeN
Start date: December 12, 2019
Phase: N/A
Study type: Interventional

Urinary tract infection (UTI) is the most common serious bacterial infection among infants. Suprapubic aspiration and bladder catheterization are considered as the gold standard by the American Academy of Pediatrics for the diagnosis, yet it is painful and invasive. In contrast, the bladder stimulation technique has been shown to be a quick and non-invasive approach to collect urine in young infants. Actually, the investigators don't have data on bacterial contamination rates for clean-catch midstream urine collections using this technique

NCT ID: NCT03801122 Completed - Clinical trials for Hematological Malignancies Treated With Intensive Chemotherapy

Evolution of Thromboelastography During Tranexamic Acid Treatment

TTRAP-Bleeding
Start date: March 5, 2019
Phase: Phase 2
Study type: Interventional

Patients with hematological malignancies are at increased risk of bleeding, especially during intensive chemotherapy. The aim of this study is to compare by thromboelastography changes during the intensive chemotherapy in patients with hematological malignancies.

NCT ID: NCT03801070 Completed - Clinical trials for Walled Off Pancreatic Necrosis (WON)

Rad Predictors for WON

Start date: July 14, 2017
Phase:
Study type: Observational

This is a retrospective chart review study examining 1) demographic data such as age, sex, etiology of pancreatitis 2) clinical data including radiological characteristics of walled off pancreatic necrosis, walled off necrosis related admissions and readmission following endoscopic drainage, surgical or percutaneous procedures performed for the management of walled off pancreatic necrosis, and clinical outcomes following treatment of WON (including hospital readmissions, WON resolution, procedure complications, WON related death) 3) endoscopy data including indication for initial endoscopic drainage and subsequent endoscopic procedures performed for management of walled off necrosis (including additional EGD's, endoscopic drainage procedures, and/or necrosectomy)

NCT ID: NCT03800966 Completed - Clinical trials for Attitudes Towards Tobacco Industry

A Brief Intervention Programme for TID

Start date: January 3, 2019
Phase: N/A
Study type: Interventional

The brief RCT will be conducted in the form of a questionnaire survey, with two kinds of leaflets embedded in the same questionnaire. The RCT will be conducted in classrooms by teachers who will be given two kinds of questionnaires (with leaflet embedded) used for intervention and control groups. The questionnaires will be mixed in a way that two adjacent questionnaires are always different. The intervention leaflets will contain information for tobacco industry denormalisation. The control leaflets will contain information for tobacco control policy in Hong Kong. The study aims to test the effect of a leaflet-based intervention on primary school students' attitudes towards tobacco industry.

NCT ID: NCT03800732 Completed - Clinical trials for Shift Work Type Circadian Rhythm Sleep Disorder

The Influence of Nocturnal Food Intake in Eating Behavior of Night Workers

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

This study aimed to verify the influence of night work and food intake during the night shift on the eating behavior of fixed night workers the next day.

NCT ID: NCT03800498 Completed - Clinical trials for Effect of Didactic Intervention Regarding (DASH) on Hypertension

Shalamar Institute of Health Sciences

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

Effect of Didactic intervention regarding Dietary Approach to Stop Hypertension (DASH) on Hypertensive Patients Blood Pressure, Knowledge and Attitude at a Tertiary Hospital of Lahore

NCT ID: NCT03800368 Completed - Psychotic Disorders Clinical Trials

Exercise and Overnight Motor Sequence Task

EOMST
Start date: December 21, 2016
Phase: N/A
Study type: Interventional

The objective of this randomized controlled trial (RCT) is to compare the changes of the sleep-related memory functions in patients with psychosis after they have completed the 12-week high-intensity exercise intervention, the 12-week low-intensity exercise intervention, or the 12-week controlled non-exercise intervention respectively. Fifty-one patients with psychosis, patients who received either the high-intensity exercise or low-intensity exercise as intervention shown a significant improvement to their impaired sleep-related memory function, while those who received non-exercise intervention has no such improvement. Moreover, high-intensity exercise may have a more prominent effect compare to low-intensity exercise.

NCT ID: NCT03800303 Completed - Clinical trials for Mood Disorders in Children and Adolescents

Integrated Treatment for Youth With Mood Disorders

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

In an effort to understand the effects of evidence-based interventions on children and adolescents, the aims of this study are to: 1. evaluate the feasibility of utilizing wearable devices to track health information (i.e., sleep, physical activity); 2. evaluate the effectiveness of evidence-based intervention components on mood and interpersonal functioning, family engagement, and sleep and physical activity level outcomes.