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Amino Acid Supplement

Leucine Enriched Amino Acids for Muscle Recovery

N/A
Waitlist Available
Research Sponsored by Daniel Moore
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6-9 months
Awards & highlights

Study Summary

This trial will look at how leucine-enriched amino acids affect muscle protein synthesis following exercise and at rest. It will also look at how this affects molecular regulation in the body.

Who is the study for?
This trial is for healthy, recreationally-active men and women aged 18-35 who haven't done resistance exercise or plyometrics in the last 3 months. Women must have a regular menstrual cycle. Exclusions include tobacco or illicit drug use, recent participation in similar studies, and recent birth control use.Check my eligibility
What is being tested?
The study tests if leucine-enriched amino acids (LEAA) are more effective than a carbohydrate placebo at incorporating specific markers into muscle proteins after exercise and at rest. It also looks at how these substances affect protein synthesis on a molecular level.See study design
What are the potential side effects?
Potential side effects aren't specified but could include digestive discomfort or allergic reactions due to the intake of LEAA compared to the carbohydrate placebo.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6-9 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6-9 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Myofibrillar Protein synthesis
Secondary outcome measures
Collagen
Protein localization via immunofluorescence
Protein Synthesis Inhibitors
Other outcome measures
Isolation of primary myoblasts for in vitro nutritional experiments

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Leucine enriched essential amino acidsActive Control1 Intervention
Leucine enriched essential amino acids (4g total, of which 1.6g are leucine). 20g carbohydrate, 2g of protein free drink powder, and 5g of Splenda to mask taste.
Group II: Carbohdyrate PlaceboPlacebo Group1 Intervention
Iso-caloric placebo (4g maltodextrin to replace LEAA). 20g carbohydrate, 2g of protein free drink powder, and 5g of Splenda to mask taste.

Find a Location

Who is running the clinical trial?

Daniel MooreLead Sponsor
2 Previous Clinical Trials
20 Total Patients Enrolled

Media Library

Leucine enriched amino acids (Amino Acid Supplement) Clinical Trial Eligibility Overview. Trial Name: NCT05554653 — N/A
Interventional. Research Study Groups: Leucine enriched essential amino acids, Carbohdyrate Placebo
Interventional. Clinical Trial 2023: Leucine enriched amino acids Highlights & Side Effects. Trial Name: NCT05554653 — N/A
Leucine enriched amino acids (Amino Acid Supplement) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05554653 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is enrollment available to those aged under 30 for this examination?

"To be eligible to join this clinical trial, patients must fall in the 18-35 year old age range. There are additional trials available for minors and seniors respectively."

Answered by AI

How many participants has the clinical trial recruited thus far?

"Confirmed. Records taken from clinicaltrials.gov indicate that this medical trial has been actively recruiting since October 1st 2022 and is still looking for 10 participants at a single site as of January 31st 2023."

Answered by AI

Does this research project currently require volunteers?

"Affirmative. The clinical trial registry states that this research is recruiting subjects and was initially posted on October 1st 2022, with its most recent update taking place at the end of January 2023. This study requires 10 participants to be enrolled from one location."

Answered by AI

Am I eligible to partake in this research study?

"This clinical trial seeks 10 healthy volunteers, between 18 and 35 years of age who meet the criteria for interventional study participation. Specifically, applicants must have completed the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+), not taken part in resistance exercise or lower body plyometrics within 3 months prior to enrollment, possess a regular menstrual cycle if female (25-35 days) over the same timespan, and commit to abiding by all rules associated with this experiment."

Answered by AI
~3 spots leftby Apr 2025