Citrulline Challenge Study for Healthy Subjects in the United Kingdom
NCT02772861 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2016-05-16
Summary
There are many forms of small bowel disease but their direct consequences on small bowel function are often very hard, if not impossible, to establish. It would be helpful if there was a reliable blood test to find out how well cells in the intestine are working. The amino acid citrulline is produced mainly by these cells, and therefore holds promise as a biological marker. Some previous studies have shown that fasting citrulline gave a good indication as to how many intestinal cells were present. However, other authors have not been able to confirm this.
Most of the citrulline in the blood is derived from another amino acid, glutamine, in a metabolic process that occurs in the intestinal cells, and most of the remainder comes from another amino acid, arginine. A further potential marker of intestinal cell function is the amino acid 3-methylhistidine. It is possible that a dynamic test, which incorporates time for conversion from one amino acid to another in the intestinal cells, might perform better.
The investigators therefore propose a study of oral glutamine, arginine, and 3-methylhistidine compared with citrulline itself or placebo (glucose) as it is hypothesized that these might increase the amount of citrulline more reproducibly. An initial study in healthy subjects is required to establish whether this is true, and if so to provide a normal range prior to investigation of patients who have or who might have the short bowel syndrome, and in whom the test would be clinically useful.
In this study, the subjects will take each of the amino acids and placebo in random order. Between each 6 hour-long visit the subjects will have at least one week where they are independent of the research team and during which they can behave normally. During each visit subjects will have a sequence of blood samples from an in-dwelling venous cannula, taken before and over 6 hours after a single small oral dose of that day's amino acid given as a small volume drink. Urine will also be collected for amino acid assay.
Conditions
- Intestinal Diseases
Interventions
- DIETARY_SUPPLEMENT
-
Amino Acid Supplement - One dose
20gr
- DIETARY_SUPPLEMENT
-
3-Methylhistidine
120mgr
Sponsors & Collaborators
-
University College, London
lead OTHER
Principal Investigators
-
Alastair Forbes, MD, FRCP · University College London, Centre for Gastroenterology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-08-31
- Primary Completion
- 2012-05-31
- Completion
- 2012-05-31
Countries
- United Kingdom
Study Locations
More Related Trials
-
Effect of L-Citrulline Supplementation on NAFLD in Adolescents With Obesity
NCT04871360 ·Status: COMPLETED ·Phase: NA
-
BCAA vs. Rifaximin in Patients With Cirrhosis for Secondary Prophylaxis of HE
NCT06538077 ·Status: RECRUITING ·Phase: PHASE4
-
A Trial of Taurine Supplementation in Parenteral Nutrition 1
NCT00135044 ·Status: UNKNOWN ·Phase: NA
-
Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Extension Study for Subjects Previously Enrolled in Triheptanoin Studies
NCT02214160 ·Status: COMPLETED ·Phase: PHASE2
-
Intralumenal Effects on Cholesterol Absorption/Synthesis
NCT00328211 ·Status: COMPLETED ·Phase: NA
-
Clinical Outcome of Triheptanoin Treatment in Patients With Long-chain Fatty Acid Oxidation Disorders (LC-FAOD) Treated Under Expanded Access Program
NCT03768817 ·Status: COMPLETED
-
Evaluating an Amino Acid Based Medical Food w/ Diarrhea in Carcinoid Syndrome & Other NETs
NCT03722511 ·Status: COMPLETED ·Phase: PHASE2
-
Breath and Blood Ammonia Response to an Oral Protein Challenge
NCT02650245 ·Status: COMPLETED ·Phase: NA
-
Study of the Safety and Tolerability of AXA1957 in Adolescent Subjects With Non-Alcoholic Fatty Liver Disease (NAFLD)
NCT04073407 ·Status: TERMINATED ·Phase: NA
-
Ulinastatin in Severe Acute Pancreatitis
NCT01132521 ·Status: SUSPENDED ·Phase: PHASE4
-
Safely and Efficacy of ClinOleic-based Lipid Parenteral Nutrition
NCT04051840 ·Status: UNKNOWN ·Phase: PHASE1
-
Intravenous Branched Chain Amino Acids for Hepatic Encephalopathy in ACLF
NCT04238416 ·Status: COMPLETED ·Phase: PHASE1
-
The Long Term Outcomes of Micronutrient Antioxidant Supplementation in Patients With Chronic Pancreatitis
NCT04312984 ·Status: COMPLETED
-
Human Heterologous Liver Cells for Infusion in Children With Urea Cycle Disorders
NCT00718627 ·Status: COMPLETED ·Phase: PHASE2
-
Branched-chain Amino Acid Supplementation for Hepatocellular Carcinoma
NCT03908255 ·Status: WITHDRAWN ·Phase: PHASE2
-
Modulation of Secondary Bile Acids Through the Intestinal Microbiota After Consumption of a High-protein Diet.
NCT05906641 ·Status: COMPLETED ·Phase: NA
-
Prevention of Parenteral Nutrition-Associated Cholestasis With Cyclic Parenteral Nutrition in Infants
NCT01062815 ·Status: TERMINATED ·Phase: NA
-
A Prospective, Randomized, Open Label Trial of Two Doses of Oral Betaine
NCT03073343 ·Status: RECRUITING ·Phase: NA
-
Safety of Undenatured Collagen Type II (UCII) Supplement in Healthy Volunteer
NCT05002634 ·Status: UNKNOWN ·Phase: NA
-
Phase I Clinical Study of Chondroitin Sulfate for Treatment of NEC
NCT06547424 ·Status: WITHDRAWN ·Phase: PHASE1
-
A Prospective Study of EUS Guided Celiac Block
NCT00583271 ·Status: COMPLETED
-
A Feasibility Trial of OCM Supplements for the Treatment of NAFLD
NCT05720702 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Nutritional Assessment Tool and Nutritional Intervention in Childhood Chronic Liver Disease
NCT02715973 ·Status: COMPLETED ·Phase: NA
-
Testing the Potential Metabolic Effect of the Human Gut Bacterial Peptide, RUCILP, in Healthy Men
NCT06923839 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Effects of Carnitine Supplementation on Liver and Muscle
NCT03439917 ·Status: COMPLETED ·Phase: NA