Aspurus

Aspurus
Studies & Documents (2)
News (1)

Asparagus racemosus
5% Shatavarins
INCI:
SPARAGUS RACEMOSUS ROOT EXTRACT
Sectors
Nutrition
Properties
Women's Health, Urinary

Aspurus

Aspurus - For all stages of women's health

- 7 Studies - 17 Controlled Parameters - The Female Adaptogen That Matches Women's Rhythms.aspurus® features a profile of 7 precisely identified and isolated biomarkers compounds (controlled separately by HPLC), supported by innovative research and in-depth expertise (including soil and cultivation). Its 7 studies—some being already published—have demonstrated its effectiveness throughout women's lives, as well as its safety..Clinical studies (including two involving 150 women) have demonstrated the incredible efficacy of aspurus® at 300mg (pre-) or 500mg (peri- and post-menopause) across 17 parameters monitored according to a medical protocol..aspurus® is a full-spectrum extract of Shatavari root (Asparagus racemosus) studied to provide the necessary active compounds (and not just shatavarines), sourced through specific selection of soils, plants, and cultivation methods. Standardized in Shatavarins (I–IX) by HPTLC, aspurus® is obtained via a proprietary, patent-pending "soft extraction" process designed to preserve major and minor phytoactive compounds..aspurus® is made by women, for women: Waleria is a research company founded and managed by women...Key results (vs. placebo) from clinical studies:
  • Significant reduction in menopausal symptoms: hot flashes (-77% to -93%) and their severity (-85%), night sweats (-47%), insomnia (-41%), anxiety/nervousness (-55%), vaginal dryness, and loss of libido.
  • Significant improvement in quality of life (Utian QoL +35%) with progress in the areas of health, emotional well-being (fatigue: -75%), professional well-being, and sexual function (+68% for libido and sexual function, +80% for satisfaction and arousal, +90% for lubrication), with estradiol/progesterone levels normalizing by day 60.
  • Improvement in sleep (Regensburg Insomnia Scale), reporting a positive effect on sleep onset and sleep duration.
..Dosage:
  • Perimenopause study (data on file): two studies over 3 months, >150 women, 500mg/day
  • Sexual wellness study (data on file): 8 weeks, 70 women, improved libido/satisfaction, 300mg
..Use/Formulation
  • Soluble powder suitable for capsules/tablets and also sticks to be diluted or orally disintegrating…
  • Recommended daily dosage (published study): 300mg/day to 500mg (250mg x 2)
  • Applications: menopausal comfort, sexual function, hormonal balance support, "female adaptogen," fatigue, night sweats, vaginal dryness
  • Several possible claims with shatavari for women's health: reducing PMS symptoms, supporting and maintaining physiological balance during and after menopause, etc.
  • Dedicated website: https://aspurusshatavari.com/

Shatavari [Asparagus r]

Shatavari - The femal adaptogen

Shatavari, or Asparagus racemosus, has long been used in Ayurveda, the traditional medicine of India, as a tonic regenerator of the female reproductive system, and much more. The ancient Ayurvedic practitioner, Sushruta (2700 B.C.) used Varuna (Crataevo religioso) and Shatavari already.

Aspurus

Supporting women’s health across hormonal transitions. From hot flashes and fatigue to intimacy and quality of life !

The female adaptogen that
matches the rhythm of women

• 7 Studies • 17 parameters controlled •

 

aspurūs® is manufactured using a clean label, patent pending extraction process that is backed by innovative research and deep rooted expertise (incl. soil and cultivation), with a designed profile of 7 bioactives, precisely identified and isolated.

Supports enhancing sexual health

Published studies 300mg (pre-) and 500mg (peri- and post-)

Safety and mechanistic studies

Reduces menopausal symptoms

Improves hormonal cognitive function

From hot flashes and fatigue to intimacy and quality of life

Supporting women’s health across hormonal transitions

 

Safety & Precautions

  • Non GMO
  • Clean Label Extraction Process
  • Rigorously Tested for Toxicity and Heavy Metals

Our trusted sourcing and unique proprietary extraction process ensure the highest quality of batch-to-batch consistency. aspurūs® is backed by preclinical and clinical studies and helps to alleviate and ease menopausal symptoms.

 

 

Sustainability + Social Responsibility

For each kilogram of aspurūs™ sold, we provide one month’s supply to women in underserved communities, fostering economic empowerment and addressing non-communicable health challenges. Our commitment extends non-GMO ingredients, and adherence to GMP compliance. Our raw materials are either cultivated by trusted farmers or responsibly wild-harvested, ensuring sustainability. Processing takes place in facilities renowned for their safety and quality standards.

Many current Shatavari extracts employ saponins as the reference biomarker, measured through the gravimetric method. However, we advocate Shatavarins as the ideal quantification standard. These powerful compounds have been identified as the primary active phytoconstituents within Shatavari

Unlike the gravimetric method, which tends to yield inconsistent and less accurate results, we employ HPTLC (High-Performance Thin-Layer Chromatography) for a more reliable assessment. This choice stems from our commitment to precision and efficacy.

aspurūs®... the ingredient by women for women.

 

The female adaptogen

As an adaptogen, it works primarily by modulating the Hypothalamic-Pituitary-Adrenal (HPA) axis, which helps the body normalize cortisol levels and maintain physiological balance (homeostasis) under physical and emotional stress. Clinical data underscores the profound cortisol-modulating capacity of aspurus® across diverse demographic profiles, a recent prospective study involving perimenopausal cohorts, by day 84, clinical supplementation with aspurus® elicited a statistically significant 17% reduction in basal serum cortisol, indicating stabilized HPA-axis reactivity. This physiological modulation correlated with a 52% decrease in perceived stress and a 74% reduction in fatigue. In another study notably, aspurus® revealed heightened efficacy in younger cohorts presenting with Female Sexual Dysfunction (FSD), characterized by 32% attenuation in cortisol and a 60% reduction in fatigue. This substantial reduction in the physiological stress burden directly correlated with improved scores in psychosexual health markers, suggesting that by mitigating cortisol, aspurus® aids in restoring the metabolic and emotional equilibrium necessary for healthy sexual function and long-term vitality. A third study in the menopausal demographic demonstrated a 44% reduction in perceived stress and an 8% decrease in fatigue.

 

The specific adaptogenic actions of aspurūs

The specific adaptogenic actions of aspurūs® are driven by its rich matrix of phytoconstituents, where Shatavarins I-IV act as estrogen receptor modulators to buffer hormonal stress, while alkaloids  support the nervous system to reduce irritability and anxiety. By neutralizing free radicals and inhibiting pro-inflammatory markers, the extract also provides a "cooling" effect that protects vital tissues from oxidative damage caused by chronic stress. This clinically validated profile makes offers a non-hormonal, plant-based product for enhancing long-term resilience and vitality throughout various stages of life.

These data suggest that aspurūs® functions as a potent adaptogen for female, normalizing endocrine stress responses across distinct female life stages.

1. Efficacy and Safety of Shatavari Root Extract for the Management of Menopausal Symptoms: A Double-Blind, Multicenter, Randomized Controlled Trial: Cureus. 2024 Apr 8;16(4):e57879. doi: 10.7759/cureus.57879.

2. A Prospective, Randomized, Single center, Double-Blind, Parallel-group, Placebo controlled Clinical Trial to evaluate the safety and the efficacy of Shatavari in women with decreased libido: under review

3. Efficacy and Safety of Shatavari Root Extract in Managing Peri-menopausal Symptoms- A Randomized, Double-Blind, Placebo Controlled Clinical trial: under review

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