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Fasting clinical trials

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NCT ID: NCT03155776 Completed - Fasting Clinical Trials

Estimation of Preoperative Gastric Volume Using Ultrasound

GUS
Start date: June 15, 2017
Phase:
Study type: Observational

Aspiration of gastric contents can be a serious anesthetic related complication. Gastric antral sonography prior to anesthesia may have a role in identifying pediatric patients at risk of aspiration. The investigator examined the relationship between sonographic antral area and endoscopically suctioned gastric volumes infants.

NCT ID: NCT03098381 Completed - Fasting Clinical Trials

Alteration in Body Composition and Metabolic Profile During Ramadan Fasting in Healthy Men

Start date: June 2016
Phase: N/A
Study type: Observational

One of religious duties for all healthy adult Muslims is fasting during Ramadan, the ninth month of Islamic lunar calendar. In this month, Ramadan observance fasted (no food and drink) from dawn to dusk. Studies demonstrated daytime fasting may pose a positive significant effect on metabolic health. Thus, this present study aimed to determine the effect of Ramadan fasting on body composition, metabolic profile, serum leptin and adiponectin levels in healthy men.

NCT ID: NCT03017066 Completed - Fasting Clinical Trials

Ultrasound Assessment of Preoperative Gastric Volume in Children

Start date: June 12, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the gastric volume in pediatric patients who followed preoperative fasting guideline using ultrasound.

NCT ID: NCT02957435 Withdrawn - Healthy Subjects Clinical Trials

Pharmacokinetics Study of Eplerenone Coated Tablets

Start date: July 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetics profile of the formulation of eplerenone coated tablets in the concentration of 25mg, 50mg and 100mg (2 coated tablets of 50mg) in male and female healthy subjects under fasting condition.

NCT ID: NCT02884791 Completed - Fasting Clinical Trials

FGF21 and Fructose Challenge in Humans

Start date: February 2016
Phase: N/A
Study type: Interventional

The primary aim of this study is to examine the effect of acute ingestion of fructose on serum FGF21 levels. Subjects in this study will be lean volunteers and individuals with metabolic syndrome.

NCT ID: NCT02843256 Completed - Obesity Clinical Trials

Using Exhaled Air to Determine Changes in Nutritional Status of Patients on Intravenous Nutrition

UEAIVN
Start date: June 8, 2016
Phase: N/A
Study type: Observational

Carbon-12 and carbon-13 are naturally-occurring isotopes that are found in exhaled breath. Investigators have proved that the 13CO2/12CO2 breath delta value (BDV) changes in subjects who were in negative energy balance then fed a positive energy balance meal. Measuring one liter of exhaled breath daily may be a more convenient way to measure negative or positive energy balance in patients receiving intravenous nutrition.

NCT ID: NCT02810977 Completed - Fasting Clinical Trials

Ultrasound Assessment of Gastric Content and Volume

Start date: June 2016
Phase: N/A
Study type: Observational

Anesthesiologists try to avoid complications with significant peri -operative morbidity and mortality such as bronchoaspiration in patients requiring a surgical procedure under anesthesia. Currently, this is achieved based on experts recommendations from the American Society of Anesthesiologists. However, there are tools like ultrasound that allow assessment of gastric content and volume. This tool allows to individualize each patient and base the decisions objectively. The investigators will assess gastric content and volume by ultrasound in patients who have fasted and require surgery at two University Hospitals.

NCT ID: NCT02773199 Completed - Ischemia Clinical Trials

Effects of Preoperative Fasting on ECG and Vital Parameters

Start date: May 2016
Phase: N/A
Study type: Observational

This study compares differences in hemodynamic ve ECG parameters of patients undergoing urological or orthopedic surgery under spinal anesthesia. First group will comprise of patients undergoing surgery in the morning hours; thus with a standard fasting duration (8 hours), and the second group will comprise of patients undergoing surgery afternoon; thus having a prolonged fasting duration (>12 hours).

NCT ID: NCT02720133 Completed - Fasting Clinical Trials

Ramadan Fasting Effects in Patients With Cardiovascular Risk Factors

Start date: July 2013
Phase: N/A
Study type: Observational [Patient Registry]

Ramadan Fasting has multiple effects on the variation of hematological and biochemical parameters.

NCT ID: NCT02710721 Completed - Prostatic Neoplasms Clinical Trials

Fasting and Nutritional Therapy in Patients With Advanced Metastatic Prostate Cancer

Start date: April 2016
Phase: N/A
Study type: Interventional

The aim of this trial is a first evaluation of the effectiveness of intermittent fasting as a supplementary therapy in patients with CRPC or hormone-sensitive prostate cancer with high metastatic load (1≥ visceral and ≥4 osseous metastases) in respect to quality of life, reduction of side effects and possible reduction in tumor progression.