Fasting

19

Review clinical trials related to Fasting. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study of Orforglipron (LY3502970) in Participants With Type 2 Diabetes Who Observe Ramadan Fasting

The purpose of this study is to test the efficacy and safety of orforglipron in participants with T2D (type 2 diabetes) who participate in fasting during Ramadan. For each participant, the study will last up to 48 weeks with a minimum of 7 in clinic visits and 4 virtual visits.

Participants needed: 130
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Eli Lilly and CompanyUpdated: Jun 23, 2026Locations: 37
Eligibility criteria

Have a clinical diagnosis of T2D based on the World Health Organization (WHO) cl... [+4]

Have any form of diabetes other than T2D, including type 1 diabetes (T1D), gesta... [+6]

Status: Recruiting

Preoperative Fasting vs. Not Fasting in Critically Ill Patients

The goal of this clinical trial is to learn if fasting or not fasting before a procedure has an effect on recovery in those who are critically ill. The main questions it aims to answer for patients on a breathing machine who are receiving tube feeding are: * Does the risk of lung complications and death differ between those who are not fasting, which may have a higher chance of allowing tube feeding to enter the lungs, and fasting, which temporarily stops nutrition before a procedure? * Is there a difference in recovery times, hospital stays, infection rates, need for organ support, safety, and nutrition for those who either fast or do not fast before a procedure? * What is the relationship between nutrition and clinical outcomes? Researchers will compare not fasting and fasting to see if it has an effect on recovery. Participants will: * Be assigned by chance (like a coin toss) to one of two groups. One group (fasting group) will have their tube feeding stopped at least 8 hours before their procedure. The other group (not fasting group) will have their tube feeding stopped right before their procedure. * Be monitored via medical record for amount of protein and calories received, and any complications related to fasting/not fasting. * Data from routine electronic medical records will be reviewed to determine how participants are doing 3 months after their procedure. '

Participants needed: 1,072
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Jun 12, 2026Locations: 19
Eligibility criteria

1. Age ≥ 18 [+13]

Inability to obtain informed consent [+14]

Status: Not yet recruiting

Mitophagy and Mitochondrial DNA Dynamics During Ramadan Dry Fasting vs 16:8 Time-Restricted Feeding

This study investigates how different types of fasting affect cell health, specifically focusing on how mitochondria (the energy-producing parts of cells) are cleared and renewed. While standard intermittent fasting allows water intake, Ramadan dry fasting involves total restriction of both food and fluids from dawn to sunset. Researchers want to see if the combined effects of fluid restriction and natural daily body rhythms during Ramadan trigger a stronger cellular cleanup process (called mitophagy) compared to standard 16:8 water-permitted fasting. The study will look at how these fasting habits change blood markers related to mitochondrial DNA and metabolic health across a 30-day period. This research will help determine if dry fasting offers distinct biological benefits for cellular renewal.

Participants needed: 120
Trial details
Age: 18-50Biological sex: AllType: ObservationalSponsor: Bahcesehir Cyprus UniversityUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Age 18-50 years [+7]

Established type 1 or type 2 diabetes (HbA1c 6.5% or higher or pharmacological a... [+6]

Status: Recruiting

The Meta-SHIFT Study: How Metabolic Shift Shapes Human Immunometabolism - a Fasting Trial

During fasting, the body shifts from using carbohydrates to relying more on fat as its main source of energy. This process is known as the 'metabolic shift'. Fat tissue helps supply this energy by breaking down stored fat into fatty acids, which are released into the bloodstream and transported to organs throughout the body. In addition to fatty acids, many other substances in the blood (such as metabolites) change during fasting to help maintain normal body function. Immune cells also circulate in the blood and play an important role in protecting the body against infections and diseases such as cancer. However, it is not yet well understood how the metabolic shift during fasting affects immune cell function. The purpose of this study is to investigate how 24 hours of fasting influences immune cell metabolism and function.

Participants needed: 28
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cornell UniversityUpdated: May 7, 2026Locations: 1
Eligibility criteria

Apparently healthy [+4]

Diagnosed with any chronic medical condition that can interfere with the study o... [+15]

Status: Recruiting

Comparison of Residual Gastric Volume Between Children Who Drink Different Clear Oral Fluid Volume

According to the American Society of Anesthesiologists (ASA) fasting guideline for patients undergoing elective surgery, the 2-hour fasting period is suggested for clear oral fluid (including water, pulp-free juice and tea or coffee without milk). This guideline does not give any suggestions for proper volume of clear oral fluid intake. This study is a prospective randomized control trials in children aged 13 through 17 years who are scheduled for an elective upper GI endoscopy procedure in the Gastroenteral Procedure Unit (GPU) at Boston Children's Hospital. The participants will be randomly assigned into one of four groups: Group 1 will consume 3 ml/kg of clear fluid by mouth at 2-hour period before surgical scheduled time, Group 2 will consume 5 ml/kg, Group 3 will consume 7 ml/kg, and Group 4 will consume 10 ml/kg. The investigators plan to recruit 72 patients in each group and 288 patients for the whole study. Research team will collect patient's demographic data, vital signs, information about their EGD procedure. Then actual volume of the stomach content and acidity will be measured from the content that is suctioned from patient's stomach during upper GI endoscopy procedure. The investigators believe that the information from this study will help establish a comprehensive NPO guideline.

Participants needed: 288
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: Boston Children's HospitalUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

ASA classification: I and II [+4]

Emergent EGD procedures [+3]

Status: Not yet recruiting

The Food Effect on Pharmacokinetics of Fixed Dose Combination of Gemigliptin/Dapagliflozin/Metformin in Healthy Volunteers

This is a single dose, randomized, open-label, two-way crossover study to investigate the food-effect bioavailability of the fixed-dose combination of Gemigliptin/Dapagliflozin/Metformin 50/10/1000 mg in healthy volunteers under fasting and fed conditions.

Participants needed: 28
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: LG ChemUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Healthy Thai male and female subjects between the ages of 18 to 55 years. [+6]

History of allergic reaction or hypersensitivity to gemigliptin or dapagliflozin... [+6]

Status: Recruiting

Gastric Assessment of Pediatric Patients Undergoing Surgery

The goal of this pilot prospective cohort study is to examine the reproducibility of gastric volume and emptying as measured by gastric ultrasound and its correlation to a gold-standard test for gastric emptying in the perioperative period in pediatric patients. The main questions it aims to answer are: * What is the reliability (inter-rater variability between expert and novice assessors, and intra-rater variability) of a) the gastric antral cross-sectional area (CSA) and b) gastric volume using the Perlas US qualitative grading assessment, measured by using an ultrasound device in pediatric patients undergoing general anesthesia for elective surgery? * What is the correlation between ultrasound assessment of gastric emptying by the antral-CSA and gastric emptying determined by the acetaminophen absorption test (AAT), the gold standard? The study will include two cohorts. Cohort assignment will be based on age and anesthesia induction plan. Subjects \>7yrs of age and expected to get an IV induction will be assigned to Cohort #1. Subjects \<7yrs of age and not expected to get an IV induction will be assigned to Cohort #2. * Cohort 1 will include abdominal ultrasound for gastric assessment AND the acetaminophen absorption test which includes administering enteral acetaminophen (tylenol) with 6 oz of water and drawing of blood samples through a peripheral intravenous line. * Cohort 2 will include subjects for whom a peripheral intravenous line placement is not part of routine pre-operative care. Procedures for Cohort 2 will include abdominal ultrasound only in the pre-op area (no tylenol). This cohort is included to examine the reliability of measurements across age groups.

Participants needed: 60
Trial details
Age: 2-18Biological sex: AllType: ObservationalSponsor: Boston Children's HospitalUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Perioperative patients with ASA classification 1-2 [+2]

History of gastrointestinal surgery [+5]

Status: Recruiting

Effect of Fasting on Patient Outcomes After Wide-Awake, Local Anesthesia-only, No Tourniquet (WALANT) Procedures

The purpose of this study is to determine whether eating solid food prior to undergoing a wide awake local-only no tourniquet (WALANT) procedure reduces anxiety in patients or has any effect on outcomes. Patients will be split randomly into two groups and told whether to eat or fast before their procedure. We will then compare levels of anxiety and nausea on the day of the procedure as well as satisfaction with the procedure and other outcome measures at follow-up visits. Our hypothesis is that patients who are instructed to eat before their WALANT procedure will have less anxiety, nausea, and overall higher satisfaction compared to those who are instructed to fast prior to their procedure.

Participants needed: 134
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of California, IrvineUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Patients undergoing wide-awake, local anesthetic-only, no-tourniquet (WALANT) pr...

Patients with insulin-dependent diabetes or allergy to local anesthesia, < 18 ye...

Status: Recruiting

Non-inferiority of Continuing Oral Intake Versus Fasting in Patients With Acute Respiratory Failure

Fasting in intensive care is mainly studied in mechanically ventilated patients or those in the weaning phase. Recent research challenge the common assumption of fasting and suggests that continuing enteral nutrition before extubation may be beneficial. Fasting is also practiced before procedures (e.g., tracheostomy, endoscopy) or surgeries, based on anesthetic guidelines. Yet, no data address fasting in non-intubated ICU patients with acute respiratory failure, despite frequent caloric deficits and inadequate nutritional intake. Aspiration risk often justifies fasting, but studies indicate that swallowing reflexes remain intact in patients receiving high-flow nasal oxygen or non-invasive ventilation. Moreover, although intubation carries a 2-5.9% aspiration risk, rapid sequence induction mitigates this, questioning the necessity of preventive fasting. Despite its prevalence, this practice lacks scientific validation and guideline support. Patient discomfort is also significant. Hunger and thirst are major sources of distress, and evidence from anesthesiology suggests that allowing fluid intake pre-anesthesia reduces discomfort. Extrapolating these findings to ICU patients could improve well-being. In conclusion, fasting in ICU patients may contribute to discomfort, dehydration, and malnutrition, while its protective benefits remain uncertain. We hypothesize that maintaining oral intake does not increase the risk of intubation or aspiration-related complications.

Participants needed: 754
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToursUpdated: Feb 18, 2026Locations: 14
Eligibility criteria

Male or female ≥ 18 years old [+6]

Persistent or worsening respiratory failure (respiratory rate > 40/min, respirat... [+12]

Status: Recruiting

Immunomodulatory Effects of Fasting in Healthy Adults

This is a clinical trial assessing the effects of fasting on the immune system in healthy adults. Immune profiling, gene expression profiling, and flow cytometry on peripheral blood mononuclear cells (PBMCs) will be performed and we hypothesize that a period of fasting will alter the immune system in healthy adults.

Participants needed: 4
Trial details
Age: 20-40Biological sex: AllType: InterventionalSponsor: University of California, DavisUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Age: 20-40 years, to constitute a young study population [+7]

Current smoking [+10]

Status: Recruiting

Fastomics: Metabolic and Therapeutic Effects of Prolonged Fasting

This is an observational study investigating how the metabolic and cell marker changes in Prolonged Fasting in the serum may be used against a cell-based model of disease for therapeutic purposes.

Participants needed: 15
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: University of MinnesotaUpdated: Oct 15, 2025Locations: 1
Eligibility criteria

Ages of 18-65 years old [+4]

Concern for active eating disorder per screening questionnaire [+4]

Status: Recruiting

Mechanisms of Fasting Induced Reduction in Energy Expenditure

Fasting reduces the energy consumption of the human body. The extent of this adaptation varies significantly between different individuals. The aim of this research project is to investigate how this adaptation of the metabolism is regulated by the body. For this purpose, we will first measure how the so-called basal metabolic rate of the body reacts to a short-term fasting of 24 h in a preliminary study. Those subjects with a particularly pronounced and those subjects with an only slightly pronounced reaction of the basal metabolic rate will be invited to the main study. Here, in random order (24 h fasting vs. 8 h fasting), the following is compared * how the basal metabolic rate of the body reacts to the reduced energy intake. * how the energy metabolism increases after a test meal * what role in particular the thyroid hormones play in this adaptation. In addition, a sample of the subcutaneous adipose tissue is taken in each case and it is examined how the regulation of metabolic processes at the cellular level.

Participants needed: 40
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: ETH ZurichUpdated: May 30, 2025Locations: 1
Eligibility criteria

Age: 18 to 40 years [+1]

Chronic conditions necessitating medical treatment (e.g., renal failure, hepatic... [+7]

Status: Not yet recruiting

Therapeutic Fasting and Immune Aging

Immunosenescence is the age-related decline of the immune system, involving a state of chronic inflammation and a decrease in the diversity/adaptability of the lymphocyte repertoire. The consequences of immunosenescence are multiple, including increased susceptibility to infections and poorer vaccine responses.

Participants needed: 20
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de Saint EtienneUpdated: Apr 8, 2025Locations: 5
Eligibility criteria

Patient affiliated or entitled to a social security scheme [+4]

Inability and/or unwillingness to follow dietary recommendations and/or perform... [+10]

Status: Recruiting

Postprandial Metabolome and Metabolic Flexibility

Metabolic flexibility is a process in which the body can switch energy substrates in different physiological states. This flexibility plays an important role in an individual's health because losing it increases the risk of obesity, metabolic syndrome, insulin resistance, and type 2 diabetes. Considering that humans spend most of their awakening hours in a postprandial (PP) state, an organism's metabolic flexibility (MF) to respond to a standardized meal's consumption would provide information on the individual's metabolic health. The PP response to glucose following an oral glucose tolerance test or consumption of a high-carbohydrate meal is well described; however, few studies assess the FM and PP metabolome using mixed meals with different macronutrients. The investigators address how metabolic flexibility and metabolome change after consuming standardized meals with different macronutrient ratios. Data collection includes clinical and diet information, indirect calorimetry, and capillary blood sampling during fasting and after consumption of standardized meals. Samples are collected weekly for one month. The data will determine the metabolic flexibility and metabolome after consuming standardized meals with different macronutrient ratios.

Participants needed: 300
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Instituto Nacional de Medicina GenomicaUpdated: Mar 17, 2025Locations: 1
Eligibility criteria

be over 18 years of age and under 30 years of age; [+3]

subjects with any pathology that requires medication or special treatment, such... [+6]

Status: Recruiting

The Impact of a 48-hour Fast with or Without Exercise on Immune Cell Metabolism and Glycemic Control in Healthy Active Adults

Many individuals engage in fasting for its purported health benefits but the effects of fasting on immune cell and whole body metabolism are not well understood in humans. Moreover, how exercising during a prolonged fast impacts immunometabolic outcomes is unclear. This study will determine how a 2 day fast - performed with or without daily exercise - impacts immune cell bioenergetics, immune cell function, and whole-body glycemic control in healthy active individuals.

Participants needed: 15
Trial details
Age: 19-35Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Mar 7, 2025Locations: 1
Eligibility criteria

Aged between 19 and 35 years. [+1]

History of cardiometabolic diseases or inflammatory diseases (e.g., chronic obst... [+7]

Status: Recruiting

Fasting Effects on Metabolism and Immunity Study in Human

This study aims to investigate the effects of 1-week fasting but not prohibiting water drink on human immune function, metabolic indicators, and brain function in human, and to explore the underlying mechanisms of these changes from a multi-omics perspective and/or other ways.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Xuanwu Hospital, BeijingUpdated: Jan 22, 2025Locations: 1
Eligibility criteria

Age 18-65 years old, gender is not limited; [+3]

Women planning pregnancy, pregnancy and breastfeeding; [+4]

Status: Not yet recruiting

Bioequivalence Study of Sulfadoxine/Pyrimethamine 500/25 mg Dispersible Tablet

The primary objective of this study is to assess the bioequivalence between the test product and the reference product based on Cmax and AUC0-\>72 for sulfadoxine and pyrimethamine in healthy adults under fasting conditions. The secondary objectives of present study are to describe the Tmax and assess the safety and tolerability profile of both test and reference products.

Participants needed: 46
Trial details
Phase: Phase 1Age: 18-50Biological sex: AllType: InterventionalSponsor: Swiss Pharma Nigeria LimitedUpdated: Jul 26, 2024Locations: 1
Eligibility criteria

Healthy subjects male or female (childbearing potential or surgically sterile fe... [+8]

Medical demographics performed not longer than two weeks before the initiation o... [+12]

Status: Recruiting

Safe Brain Initiative, Operationalizing Precision Anaesthesia

Perioperatively, patients experience an unnecessarily high level of side effects associated with their treatment. These side effects include nausea, severe pain, anxiety, and stress. Moreover, many patients develop postoperative delirium (POD) and neurocognitive dysfunctions, often resulting in long-term cognitive impairment, decreased quality of life, and increased mortality. However, physicians, nurses and their institutions do not receive structured feedback regarding these aspects of each patient's well-being. They may therefore be unable to engage in the essential cause-and-effect learning necessary to evaluate and consecutively reduce such side effects. Effective guidelines conform prevention is the proven key to shielding our patients from adverse Outcomes. The Safe Brain Initiative's high-quality routine data-for-action is a sword and accelerator for moving towards patient-centred, precision care. Thus, establishing a foundation for value-based and patient-centred healthcare development. However, a turnkey real-world solution is challenging to develop and implement and requires substantial resources. As a result, such solutions are usually beyond the scope of a single institution. The SBI platform provides high-quality, real-world data to bridge this gap. It allows monitoring and in-depth analysis of cause and effect in the day-to-day routine of individuals, departments, and institutions. The SBI's approach is continuously improved and updated. An organization called the SBI Global Society oversees the quality and precision of science through experts in the field. At SBI Hospitals and Flagship centres, Masterclasses are conducted and can be attended alongside clinical immersions. SBI Solutions manages, develops, and provides technical and service support for the Safe Brain Initiative. Its service guarantees the professional and GDPR conform management of data handling and storage as well as the user-friendly functionality of the SBI-Dashboard solutions.

Participants needed: 15,000
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of Southern DenmarkUpdated: Jun 7, 2024Locations: 1Duration: 5 Years
Eligibility criteria

Not listed

Status: Recruiting

Effectiveness of Focused Tele-education in Reducing Diabetes Complications During Ramadan

Introduction Diabetes is a global emergency with detrimental clinical and financial consequences. Poorly managed diabetes leads to a myriad of serious complications, especially cardiovascular and infectious complications, with consequent increased cost and mortality rate. For Muslims in particular, the annual fasting month of Ramadan is one such period when diabetes control is essential. Adequate adjustments in diabetes management need to be made in line with the allowed mealtimes to avoid the risk of diabetes complications during Ramadan. Objective Investigators aim to investigate the effectiveness of Ramadan-focused structured diabetes tele-education to reduce diabetes complications during Ramadan fasting for Muslims with diabetes in South East Asia. Methodology In a parallel group randomized controlled trial, investigators aim to recruit 300 adults with diabetes who are able to fast at least 15 days in Ramadan. You will be randomized to the intervention group comprising of a Ramadan-focused structured diabetes tele-education and control group receiving standard care. You will be reviewed again after Ramadan. The primary outcome is the incidence of hypoglycemia in Ramadan. The secondary outcomes are incidence of other diabetes complications in Ramadan episodes including hyperglycemia, episodes of acute infections, attendances in clinic and emergency department, hospital admissions, and compliance to recommendations for diabetes management during Ramadan. Clinical Significance The study enables investigators to evaluate Ramadan-focused structured diabetes tele-education to reduce the risk of diabetes complications for a large population during the fasting month.

Participants needed: 300
Trial details
Age: 21-100Biological sex: AllType: InterventionalSponsor: Sengkang General HospitalUpdated: Sep 21, 2023Locations: 1
Eligibility criteria

Adults with diabetes planning to fast in Ramadan, [+8]

Severe diabetes complications including end-stage renal failure [+5]