Home Supplements How We Rate Blog
Ruscus aculeatus

Butcher's Broom

Research reviewed: Up until 03/2026

Butcher's Broom (Ruscus aculeatus) is a dietary supplement with 12 published peer-reviewed studies involving 794 participants, researched for Chronic Venous Insufficiency & Leg Oedema.

12
Studies
794
Participants
1988–2025
Research Span

Evidence at a Glance

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

Overall: Very Strong Evidence

Chronic Venous Insufficiency & Leg Oedema

Strong
12 studies 10 of 12 positive 794 participants 9 human

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

7/12
Randomised
6/12
Double-Blind
6/12
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2002)
166
Study 2 (2006)
57
Study 3 (2001)
0
Study 4 (1988)
150
Study 5 (2005)
200
Study 6 (2004)
0
Study 7 (2014)
97
Study 8 (2016)
0

Research Timeline

When the studies were published

1
1988
1
2001
1
2002
1
2004
1
2005
1
2006
1
2014
1
2016
1
2018
1
2022
1
2023
1
2025

All Studies

Detailed breakdown of each trial. Click to expand.

Chronic Venous Insufficiency & Leg Oedema

1

To assess the efficacy and safety of Ruscus aculeatus extract vs placebo in chronic venous insufficiency.

2002 166 participants 12 weeks 36–37 mg Ruscus aculeatus extract twice daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled multicentre trial

Purpose

To assess the efficacy and safety of Ruscus aculeatus extract vs placebo in chronic venous insufficiency.

Dose

36–37 mg Ruscus aculeatus extract twice daily

Participants

166 patients with chronic venous insufficiency

Duration

12 weeks

Results

Ruscus aculeatus extract significantly reduced lower leg oedema and symptom scores vs placebo. Heaviness, tension, and pain in the legs were all significantly improved. Safe and well tolerated.

How They Measured It

Lower leg volume (water displacement plethysmography), oedema rating, patient symptom scores

Read full study
2

To assess clinical and capillaroscopic improvement with Ruscus aculeatus, hesperidin methylchalcone, and ascorbic acid in venous insufficiency.

2006 57 participants 8 weeks Ruscus 150 mg + HMC 150 mg + ascorbic acid 100 mg twice dail...
Human Study RCT Positive

Study Type

Randomised, controlled, open-label trial

Purpose

To assess clinical and capillaroscopic improvement with Ruscus aculeatus, hesperidin methylchalcone, and ascorbic acid in venous insufficiency.

Dose

Ruscus 150 mg + HMC 150 mg + ascorbic acid 100 mg twice daily

Participants

57 ambulatory patients with chronic venous insufficiency

Duration

8 weeks

Results

Combination significantly improved CEAP symptom scores and capillaroscopic parameters. Microcirculatory improvements visible within 2 weeks. Appeared synergistic for venous tone and microvascular permeability.

How They Measured It

CEAP scale, symptom scores, skin capillaroscopy at 2, 4, 6, and 8 weeks

Read full study
3

To explore Ruscus aculeatus as a treatment for orthostatic hypotension and venous pooling.

2001 ? participants Variable Standardised Ruscus aculeatus extract (oral)
Human Study Positive

Study Type

Review with case report

Purpose

To explore Ruscus aculeatus as a treatment for orthostatic hypotension and venous pooling.

Dose

Standardised Ruscus aculeatus extract (oral)

Participants

Case report + literature review

Duration

Variable

Results

Ruscus aculeatus exerts venotonic and vasoconstrictive effects via alpha-adrenoreceptor stimulation. Appropriate for managing orthostatic hypotension where venous pooling is an underlying factor. Case reported significant clinical improvement.

How They Measured It

Literature review of venoconstrictor mechanisms; illustrative case report

Read full study
4

To assess the use of Ruscus aculeatus extract in venous disease of the lower limbs.

1988 150 participants 8 weeks 36–37 mg Ruscus aculeatus extract twice daily
Human Study Positive

Study Type

Open observational study

Purpose

To assess the use of Ruscus aculeatus extract in venous disease of the lower limbs.

Dose

36–37 mg Ruscus aculeatus extract twice daily

Participants

150 patients with venous disease

Duration

8 weeks

Results

Significant improvements in all venous disease symptoms including pain, heaviness, and cramps. Ankle circumference (oedema) meaningfully reduced. Physician global assessments confirmed clinical improvement in majority of patients.

How They Measured It

Patient self-assessment of venous symptoms, ankle circumference, physician global assessment

Read full study
5

To evaluate Ruscus aculeatus in reducing flight-related oedema in airline passengers.

2005 200 participants Single flight (>10 hours) 150 mg Ruscus aculeatus extract taken pre-flight
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate Ruscus aculeatus in reducing flight-related oedema in airline passengers.

Dose

150 mg Ruscus aculeatus extract taken pre-flight

Participants

200 healthy volunteers taking long-haul flights

Duration

Single flight (>10 hours)

Results

Ruscus extract significantly reduced post-flight leg oedema vs placebo (+67 mL vs +138 mL, p<0.001). Ankle circumference increase was halved. Practical preventive measure for flight-related venous pooling.

How They Measured It

Lower leg volume, ankle circumference measured before and after flight

Read full study
6

To review the pharmacological basis for Ruscus aculeatus venotonic and vasoconstrictive properties.

2004 ? participants Various Standardised Ruscus saponins (ruscogenin, neoruscogenin)
Review/Other Mixed

Study Type

Pharmacological review

Purpose

To review the pharmacological basis for Ruscus aculeatus venotonic and vasoconstrictive properties.

Dose

Standardised Ruscus saponins (ruscogenin, neoruscogenin)

Participants

Multiple preclinical and clinical studies reviewed

Duration

Various

Results

Ruscus saponins induce venoconstriction via alpha-1 and alpha-2 adrenoreceptor stimulation. They also reduce vascular permeability by inhibiting elastase and hyaluronidase. These mechanisms explain venotonic effects in venous insufficiency.

How They Measured It

Review of in vitro receptor binding, animal vasoconstriction data, and human vascular pharmacology

Read full study
7

To assess Ruscus aculeatus + hesperidin methylchalcone on venous tone in chronic venous insufficiency.

2014 97 participants 12 weeks Ruscus 100 mg + HMC 900 mg + ascorbic acid 100 mg daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To assess Ruscus aculeatus + hesperidin methylchalcone on venous tone in chronic venous insufficiency.

Dose

Ruscus 100 mg + HMC 900 mg + ascorbic acid 100 mg daily

Participants

97 patients with CEAP class C3–C4 venous insufficiency

Duration

12 weeks

Results

Active treatment significantly improved venous compliance and reduced ankle oedema vs placebo. Heaviness, pain, and leg fatigue all significantly reduced. The combination improved microcirculation and venous wall tone.

How They Measured It

Venous compliance, ankle oedema, CEAP symptom assessment

Read full study
8

To pool evidence from RCTs on the efficacy of Ruscus aculeatus-based products for chronic venous disorders.

2016 ? participants 8–16 weeks Various standardised preparations
Review/Other Positive

Study Type

Meta-analysis

Purpose

To pool evidence from RCTs on the efficacy of Ruscus aculeatus-based products for chronic venous disorders.

Dose

Various standardised preparations

Participants

Multiple RCTs included

Duration

8–16 weeks

Results

Pooled analysis confirmed significant reductions in leg oedema and symptom scores with Ruscus-based treatments. Effect sizes were moderate but clinically meaningful. Excellent safety profile across all included trials.

How They Measured It

Pooled leg oedema, symptom score, and adverse event data

Read full study
9

To investigate Ruscus aculeatus for symptoms of haemorrhoids and perianal varicose disorder.

2018 124 participants 8 weeks 150 mg Ruscus extract three times daily
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To investigate Ruscus aculeatus for symptoms of haemorrhoids and perianal varicose disorder.

Dose

150 mg Ruscus extract three times daily

Participants

124 patients with symptomatic haemorrhoids

Duration

8 weeks

Results

Ruscus extract significantly reduced haemorrhoidal symptoms including bleeding, prolapse, and pain vs placebo. Venoconstrictor properties appear effective across venous conditions beyond lower limbs.

How They Measured It

Haemorrhoid symptom score, bleeding, prolapse, pain ratings

Read full study
10

The role of venoactive compounds in the treatment of chronic venous disease

2025 ? participants See full study As per study protocol
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

The role of venoactive compounds in the treatment of chronic venous disease

Dose

As per study protocol

Participants

See full study

Duration

See full study

Results

Statistically significant findings reported — see full study for complete results.

How They Measured It

See full study for endpoints and measurement methods

Read full study
11

Systematic literature review and expert meeting report on health-related quality of life in chronic venous disease

2023 ? participants See full study As per study protocol
Review/Other Positive

Study Type

Systematic review

Purpose

Systematic literature review and expert meeting report on health-related quality of life in chronic venous disease

Dose

As per study protocol

Participants

See full study

Duration

See full study

Results

Statistically significant findings reported — see full study for complete results.

How They Measured It

See full study for endpoints and measurement methods

Read full study
12

Clinical Perspectives and Management of Edema in Chronic Venous Disease-What about Ruscus?

2022 ? participants See full study As per study protocol
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

Clinical Perspectives and Management of Edema in Chronic Venous Disease-What about Ruscus?

Dose

As per study protocol

Participants

See full study

Duration

See full study

Results

Statistically significant findings reported — see full study for complete results.

How They Measured It

See full study for endpoints and measurement methods

Read full study

Frequently Asked Questions

Common questions about Butcher's Broom research

What does the research say about Butcher's Broom?

There are currently 12 peer-reviewed studies on Butcher's Broom (Ruscus aculeatus), involving 794 total participants. Research covers Chronic venous insufficiency, Leg oedema reduction, Circulation improvement and 1 more areas. The overall evidence strength is rated as Very Strong.

How strong is the evidence for Butcher's Broom?

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 (9 human studies), and reported outcomes.

What health goals has Butcher's Broom been studied for?

Butcher's Broom has been researched for: Chronic venous insufficiency, Leg oedema reduction, Circulation improvement, Orthostatic hypotension support. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on Butcher's Broom based on human trials?

Yes, 9 out of 12 studies are human trials. Human trials carry more weight in our evidence scoring system.