Convolvulis arvensis

Convolvulis arvensis

Common Names

  • Field bindweed

For Patients & Caregivers

Leaf extract of field bindweed (Convolvulis arvensis) may stop the growth of new blood vessels. But there’s not enough evidence to show it is a safe and effective cancer treatment in humans.

Field bindweed is an invasive weed found in many parts of the world. It has been used in traditional medicine but extracts from the leaves are sold as dietary supplement. These extracts contain proteoglycans that were shown to stimulate the immune system and stop the growth of new blood vessels in lab studies.   They also reduced the size of tumors in the mice.  No clinical trials in humans have been done to find out field bindweed extracts’ benefits and adverse effects. Since these extracts affect growth of new blood vessels, they may interfere with would healing,

  • To stop blood-vessel growth and shrink tumors
    Laboratory studies in mice and chicken eggs suggest that extracts of bindweed flowers and leaves can stop blood-vessel growth.  In mice, this caused tumors to stop growing. This effect has not been tested in humans.
  • To stimulate the immune system
    One small study in rabbits suggests that field bindweed extract stimulates some cells of their immune systems, and another shows some effect on white blood cell growth.  This has not been tested in humans.
  • To lower high blood pressure
    Field bindweed has been used in traditional medicine to lower high blood pressure.
  • As a laxative
    Field bindweed has been used in traditional medicine as a laxative. No scientific evidence supports this use.
  • You use drugs that inhibit blood vessel growth, such as bevacizumab (Field bindweed extract may increase the risk of adverse effects)
  • You are pregnant, or you are a child or adolescent (Field bindweed extracts may inhibit blood-vessel growth, which is needed for fetal and child development)
  • You have a wound or injury that is healing (Field bindweed extracts may interfere with wound healing)

Consumption of large quantities of raw field bindweed caused side effects of the digestive system in animals.

Field bindweed (C. arvensis) extracts have not been tested in humans as a cancer treatment. They are not substitutes for prescription anti-cancer drugs.

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For Healthcare Professionals

C-statin, VascuStatin
Convolvulis arvensis

Convolvulis arvensis, commonly known as field bindweed, is a plant that belongs to the morning glory family. It is a perennial vine with white to pink flowers that can be found in temperate regions. C. arvensis is considered a noxious weed in US farmlands due to its invasive nature but has historical use as a medicinal plant in Europe for hypertension and as a laxative (1), and in traditional Chinese medicine for relief of itching, pain, and toothache (2).
The leaf extract is marketed as a dietary supplement to support vascular health by restricting new blood vessel growth. However, related products are also promoted as a natural cancer treatment.
Recent in vitro and animal studies show that the water extracts from the plant’s aerial parts, rich in proteoglycans, have anti-angiogenic and immune-stimulating effects (3)(4)(5)(6). Other studies found that these constituents also increased vasodilation and circulatory function, and lowered blood pressure in animals (7).

Alkaloids from raw field bindweed are toxic to animals (8)(9) but dietary supplements are alkaloid-free.
Due to its ability to inhibit new blood vessel growth, C. arvensis should not be used before and after surgery. Infants, children, adolescents, and pregnant women should also avoid this product.

Water extract from the aerial parts of C. arvensis is thought to be rich in proteoglycans. It exerts immunostimulatory effects in animals by increasing total leukocyte and lymphocyte counts as well as increasing serum lysosome activity (4). The lipophilic glycoside constituents have cytotoxic effects in human tumor cell lines (5). High molecular weight extract from C. arvensis inhibits tumor growth in a dose-dependent manner probably due to its ability to inhibit growth of blood vessels (8) .
Animal studies show that the tropane alkaloids from C. arvensis have anti-muscarinic activity that slows gastrointestinal motility. This may increase the absorption of toxins leading to intestinal fibrosis gastritis and/or hepatitis (8).

C. arvensis leaf extract inhibits vascular development (8), and can, theoretically interfere with wound healing.

Reported: In animal studies, weight loss and intestinal pain were reported after consuming large amounts of bindweed, probably due to the tropane alkaloid contents (8).

Leaf extracts of C. arvensis have anti-angiogenic activities(8), and may increase the risk of adverse effects when used with other anti-angiogenic agents, such as bevacizumab.


  1. Rexhepi B, Mustafa B, Hajdari A, et al. Genetic Resources and Crop Evolution. 2013:1-26.

  2. Zhou J GX, Xinjian Y. Isolated Compounds T-Z, References, Tcm Plants and Congeners. Encyclopedia of Traditional Chinese Medicines: Molecular Structures, Pharmacological Activities, Natural Sources and Applications. Vol 5: Springer; 2011:410.

  3. Manbir K, Kalia AN. International Journal of Pharmacy and Pharmaceutical Sciences. 2012;4(1):38-40.

  4. Al-Bowait ME, Albokhadaim IF, Homeida AM. Research Journal of Pharmacology. 2010;4(2):51-54.

  5. Sadeghi-aliabadi H; Ghasemi N; Kohi M. Research in Pharmaceutical Sciences. Mar 2008;3(1)(April 2008):31-34.

  6. Meng XL, Riordan NH, Casciari JJ, et al. Effects of a high molecular mass Convolvulus arvensis extract on tumor growth and angiogenesis. Puerto Rico health sciences journal. Dec 2002;21(4):323-328.

  7. Sowemimo BO, Farnsworth NR. Journal of Pharmaceutical Sciences. 1973;62(4):678-679.

  8. Todd FG, Stermitz FR, Schultheis P, et al. Tropane alkaloids and toxicity of Convolvulus arvensis. Phytochemistry. May 1995;39(2):301-303.

  9. Schultheiss PC, Knight AP, Traub-Dargatz JL, et al. Toxicity of field bindweed (Convolvulus arvensis) to mice. Veterinary and human toxicology. Oct 1995;37(5):452-454.

  10. Said AM, Numan IT, Hamad MN. International Journal of Pharmacy and Pharmaceutical Sciences. 2013;5(SUPPL. 2):303-305.

  11. Sher Z, Ibrar M, Hameed I. Journal of Medicinal Plant Research. 2011;5(23):5540-5544.

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