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L-Ornithine

Ornithine

Research reviewed: 2025-2026

Ornithine (L-Ornithine) is a dietary supplement with 13 published peer-reviewed studies involving 670 participants, researched for Fatigue & Sleep, Ammonia Detoxification, Athletic Performance & Growth Hormone and 5 more areas.

13
Studies
670
Participants
1990–2026
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Very Strong Evidence

Fatigue & Sleep

Strong
2 studies 2 of 2 positive 112 participants

Ammonia Detoxification

Strong
2 studies 2 of 2 positive 109 participants

Athletic Performance & Growth Hormone

Strong
2 studies 2 of 2 positive 56 participants

Liver Health & Metabolism

Moderate
2 studies 2 of 2 positive 29 participants 1 human

Cognitive Function

Moderate
2 studies 1 of 2 positive 595 participants

General Health

Moderate
1 study 0 of 1 positive 75 participants

Liver Health

Moderate
1 study 0 of 1 positive 0 participants

Heart Health

Moderate
1 study 0 of 1 positive 0 participants

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

7/13
Randomised
7/13
Double-Blind
7/13
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2014)
52
Study 2 (2016)
60
Study 3 (2015)
45
Study 4 (2000)
64
Study 5 (2012)
36
Study 6 (1990)
20
Study 7 (2010)
8
Study 8 (2022)
21

Research Timeline

When the studies were published

1
1990
1
2000
1
2010
1
2012
1
2014
1
2015
1
2016
1
2022
4
2025
1
2026

All Studies

Detailed breakdown of each trial. Click to expand.

Fatigue & Sleep

1

To evaluate L-ornithine hydrochloride on fatigue and sleep in healthy subjects with mild fatigue

2014 52 participants 8 weeks 400 mg/day L-ornithine HCl
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate L-ornithine hydrochloride on fatigue and sleep in healthy subjects with mild fatigue

Dose

400 mg/day L-ornithine HCl

Participants

52 healthy adults with self-reported fatigue

Duration

8 weeks

Results

Significant reduction in fatigue scores (p=0.01), improved sleep quality, and reduced morning ammonia levels. Mood and wellbeing also improved vs placebo.

How They Measured It

OSS fatigue scale, PSQI, Profile of Mood States, plasma ammonia

Read full study
2

To assess L-ornithine on stress-related fatigue and sleep in working adults

2016 60 participants 8 weeks 400 mg/day L-ornithine
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess L-ornithine on stress-related fatigue and sleep in working adults

Dose

400 mg/day L-ornithine

Participants

60 healthy working adults under occupational stress

Duration

8 weeks

Results

Significant reduction in fatigue (p=0.02) and sleep disturbance. Morning salivary cortisol reduced. Salivary amylase (stress marker) trending lower. Overall stress-related fatigue improved.

How They Measured It

OSS fatigue score, salivary cortisol, salivary amylase, PSQI

Read full study

Ammonia Detoxification

3

To evaluate L-ornithine supplementation on ammonia levels and fatigue after alcohol consumption

2015 45 participants Acute alcohol study 400 mg/day L-ornithine
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate L-ornithine supplementation on ammonia levels and fatigue after alcohol consumption

Dose

400 mg/day L-ornithine

Participants

45 healthy adults

Duration

Acute alcohol study

Results

Significant reduction in blood ammonia levels (p=0.01) and hangover symptom scores. Fatigue the following morning reduced. Urea cycle enhancement confirmed.

How They Measured It

Blood ammonia, ethanol metabolism, fatigue VAS, hangover scores

Read full study
4

To assess ornithine supplementation on blood ammonia in patients with liver disease

2000 64 participants 7 days 10 g/day L-ornithine L-aspartate infusion
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess ornithine supplementation on blood ammonia in patients with liver disease

Dose

10 g/day L-ornithine L-aspartate infusion

Participants

64 patients with hepatic encephalopathy

Duration

7 days

Results

Significant reduction in blood ammonia levels (p<0.001) and improvement in hepatic encephalopathy grade. Neurological function improved. Ornithine is effective in hepatic ammonia management.

How They Measured It

Blood ammonia, neurological function, hepatic encephalopathy grading

Read full study

Athletic Performance & Growth Hormone

5

To evaluate L-ornithine on strength, body composition and recovery in athletes

2012 36 participants 6 weeks 2 g/day L-ornithine
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate L-ornithine on strength, body composition and recovery in athletes

Dose

2 g/day L-ornithine

Participants

36 trained athletes

Duration

6 weeks

Results

Significant improvement in fatigue resistance during prolonged exercise (p=0.03). Post-exercise ammonia lower. Lean body mass trended higher. Recovery quality improved.

How They Measured It

1RM strength, lean mass, post-exercise fatigue, ammonia

Read full study
6

To examine the effect of oral ornithine on growth hormone secretion

1990 20 participants 4 weeks 100 mg/kg/day L-ornithine
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To examine the effect of oral ornithine on growth hormone secretion

Dose

100 mg/kg/day L-ornithine

Participants

20 healthy young men

Duration

4 weeks

Results

Significant increase in GH levels (p=0.04) after 4 weeks. IGF-1 also elevated. Lean mass trends consistent with anabolic GH effects. Urinary ornithine increased confirming absorption.

How They Measured It

Serum GH, IGF-1, arginine and ornithine plasma levels

Read full study

Liver Health & Metabolism

7

To assess L-ornithine L-aspartate (LOLA) in hepatic encephalopathy treatment

2010 8 participants Various 20-40 g/day LOLA infusion
Review/Other Positive

Study Type

Systematic review and meta-analysis

Purpose

To assess L-ornithine L-aspartate (LOLA) in hepatic encephalopathy treatment

Dose

20-40 g/day LOLA infusion

Participants

Meta-analysis of 8 RCTs

Duration

Various

Results

Significant reduction in blood ammonia and improvement in encephalopathy grade. LOLA appears effective for management of hepatic encephalopathy. Well tolerated.

How They Measured It

Blood ammonia, encephalopathy grade, neurological tests across RCTs

Read full study
8

To evaluate L-ornithine on endurance performance in kayakers

2022 21 participants 4 weeks 2 g/day L-ornithine
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate L-ornithine on endurance performance in kayakers

Dose

2 g/day L-ornithine

Participants

21 competitive kayakers

Duration

4 weeks

Results

Significant improvement in time trial performance (p=0.03). Post-exercise ammonia and blood lactate levels lower. Perceived fatigue significantly reduced vs placebo.

How They Measured It

Time trial performance, blood lactate, post-exercise fatigue, ammonia

Read full study

Cognitive Function

9

STELLAR: Phase III, Randomized, Open-Label Study of Eflornithine Plus Lomustine Versus Lomustine Alone in Patients With Recurrent Grade 3 Astrocytoma.

2026 343 participants 2 weeks See study
Human Study Mixed

Study Type

RCT

Purpose

STELLAR: Phase III, Randomized, Open-Label Study of Eflornithine Plus Lomustine Versus Lomustine Alone in Patients With Recurrent Grade 3 Astrocytoma.

Dose

See study

Participants

343 participants

Duration

2 weeks

Results

CONCLUSION: Clinically meaningful improvements were observed; eflornithine + lomustine doubled PFS and improved OS in patients with recurrent IDH-mutant, grade 3 astrocytoma, but not grade 4 tumors,.

How They Measured It

PubMed PMID: 41325560. J Clin Oncol

Read full study
10

Comparison of efficacy of rifaximin, probiotics and L-ornithine L-aspartate in overt hepatic encephalopathy: a randomized, phase IV, lactulose control

2025 252 participants Not specified See study
Human Study Mixed

Study Type

RCT

Purpose

Comparison of efficacy of rifaximin, probiotics and L-ornithine L-aspartate in overt hepatic encephalopathy: a randomized, phase IV, lactulose control

Dose

See study

Participants

252 participants

Duration

Not specified

Results

Study results available at linked source.

How They Measured It

PubMed PMID: 41272855. Trials

Read full study

General Health

11

L-ornithine supplementation in periodontitis treatment yields greater benefits than L-arginine after one year: Part II of a randomized controlled pilo

2025 75 participants 12 months See study
Human Study Mixed

Study Type

RCT

Purpose

L-ornithine supplementation in periodontitis treatment yields greater benefits than L-arginine after one year: Part II of a randomized controlled pilo

Dose

See study

Participants

75 participants

Duration

12 months

Results

CONCLUSION: After one year, L-ornithine supplementation demonstrated more pronounced clinical benefits than L-arginine, although both can modulate gingival CD68 + and CD163 + macrophages.

How They Measured It

PubMed PMID: 40614877. Complement Ther Med

Read full study

Liver Health

12

An Open-Label Randomized Controlled Non-Inferiority Trial of Arginine Glutamate Injection for the Treatment of Mild Hepatic Encephalopathy.

2025 ? participants 7 days See study
Human Study Mixed

Study Type

RCT

Purpose

An Open-Label Randomized Controlled Non-Inferiority Trial of Arginine Glutamate Injection for the Treatment of Mild Hepatic Encephalopathy.

Dose

See study

Participants

Not specified

Duration

7 days

Results

CONCLUSIONS: Both regimens effectively alleviated mild HE symptoms and reduced ammonia levels.

How They Measured It

PubMed PMID: 40545706. J Dig Dis

Read full study

Heart Health

13

The effects of acute and chronic oral tea catechins and ornithine supplementation on exercise-induced ammonia accumulation and cycling performance in

2025 ? participants 13 days See study
Human Study Mixed

Study Type

RCT

Purpose

The effects of acute and chronic oral tea catechins and ornithine supplementation on exercise-induced ammonia accumulation and cycling performance in

Dose

See study

Participants

Not specified

Duration

13 days

Results

CONCLUSIONS: A single dose and 14-day oral intake of tea catechins and ornithine supplementation did not suppress exercise-induced ammonia accumulation or enhance cycling performance.

How They Measured It

PubMed PMID: 40506665. Eur J Appl Physiol

Read full study

Frequently Asked Questions

Common questions about Ornithine research

What does the research say about Ornithine?

There are currently 13 peer-reviewed studies on Ornithine (L-Ornithine), involving 670 total participants. Research covers Fatigue reduction, Sleep quality, Ammonia detoxification and 2 more areas. The overall evidence strength is rated as Very Strong.

How strong is the evidence for Ornithine?

The evidence is currently rated as "Very Strong Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (12 human studies), and reported outcomes.

What health goals has Ornithine been studied for?

Ornithine has been researched for: Fatigue reduction, Sleep quality, Ammonia detoxification, Athletic performance, Growth hormone. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Ornithine based on human trials?

Yes, 12 out of 13 studies are human trials. Human trials carry more weight in our evidence scoring system.