Table 3.
Natural Compound | Identifier/Status | Cancer Type/Conditions | Title | Observations |
---|---|---|---|---|
Resveratrol | NCT00256334/Completed | Colon cancer | Resveratrol for Patients With Colon Cancer | Patients were randomly assigned to one of four dose cohorts: plant-derived resveratrol tablets (80 mg/day and 20 mg/day), Grape Powder dissolved in water and taken orally (120 g/day and 80 g/day). |
NCT02261844/Withdrawn (No funding) | Liver cancer | Resveratrol and Human Hepatocyte Function in Cancer | Resveratrol 1 g daily for 10 days Dietary Supplement: Resveratrol Resveratrol 1 g po x 10 days prior to liver resection |
|
NCT01476592/Completed | Neuroendocrine tumor | A Biological Study of Resveratrol’s Effects on Notch-1 Signaling in Subjects With Low Grade Gastrointestinal Tumors | 5 g/day of resveratrol orally, in two divided doses of 2.5 g each without a break in therapy for a total of three cycles | |
NCT00433576/Completed | Colorectal cancer | Resveratrol in Treating Patients With Colorectal Cancer That Can Be Removed By Surgery | STAGE II: Patients receive oral resveratrol on days 1–8 and undergo colorectomy on day 9. | |
NCT00098969/Completed | Unspecified Adult Solid Tumor, Protocol Specific | UMCC 2003-064 Resveratrol in Preventing Cancer in Healthy Participants | This phase I trial is studying the side effects and best dose of resveratrol in preventing cancer in healthy participants. | |
NCT03253913/Unknown | Lymphangioleiomyomatosis | Resveratrol and Sirolimus in Lymphangioleiomyomatosis Trial | Resveratrol 250 mg daily for the first 8 weeks, followed by 250 mg twice daily for the next 8 weeks, and then 500mg twice daily for the last 8 weeks. | |
NCT04266353/Suspended (Due to COVID-19) | Breast cancer | Effect of Resveratrol on Serum IGF2 Among African American Women | Participants with receive resveratrol at 150 mg daily for 6 weeks | |
NCT00578396/Unknown | Colon cancer | Phase I Biomarker Study of Dietary Grape-Derived Low Dose Resveratrol for Colon Cancer Prevention | - | |
Curcumin | NCT03980509/Recruiting | Breast Cancer | A "Window Trial" on Curcumin, the Active Compound in Turmeric, for Invasive Breast Cancer Primary Tumors | Curcumin (500 mg) will be orally administered twice a day, after each meal from the time surgical resection is scheduled until the night before surgical resection. |
NCT04294836/Not yet Recruiting | Cervical Cancer | Randomized Phase II Clinical Trial of Oral Turmeric Supplementation in Patients With Advanced Cervical Cancer | Curcumin administered in a dosage of 2000 mg daily, in association with cisplatin and radiotherapy for 16 weeks | |
NCT02724202/Active, not recruiting | Colon Cancer | A Pilot, Feasibility Study of Curcumin in Combination With 5FU for Patients With 5FU-Resistant Metastatic Colon Cancer | Curcumin at a dosage of 500 mg twice/day will be orally administered for 2 weeks. Patients will continue on curcumin at the same dose for an additional 6 weeks while being treated with 3 cycles of 5-fluorouracil | |
EGCG | NCT02891538/Recruiting | Colorectal Cancer | A Pilot Study to Evaluate the Chemopreventive Effects of Epigallocatechin Gallate (EGCG) in Colorectal Cancer (CRC) Patients With Curative Resections | EGCG (highly purified and refined green tea extract-Teavigo™) administered at a dosage of 450 mg twice a day |
NCT01317953/Available | Lung Cancer | Phase I Study of Oral Green Tea Extract as Maintenance Therapy for Extensive-stage Small Cell Lung Cancer | Increasing doses of EGCG (400, 800, 1200, 1600 and 2000 mg) administered daily | |
NCT00917735/Completed | Breast Cancer | Phase II, Randomized, Double-blind, Placebo-controlled, Study of the Efficacy of Green Tea Extract on Biomarkers of Breast Cancer Risk in High Risk Women With Differing Catechol-O-methyl Transferase (COMT) Genotypes | Oral administration of two Green tea extract capsules containing 51.7% EGCG, twice daily after breakfast and dinner for one year. | |
Quercetin |
NCT01538316/ Unknown |
Prostate Cancer | Clinical Trial on the Effectiveness of the Flavonoids Genistein and Quercetin in Men With Rising Prostate-specific Antigen | 500 mg of quercetin supplement (+ vitamin C + folic acid + vitamin B3) administered daily over a period of six months, followed by genistein and placebo administration. |
NCT03476330/Recruiting | Squamous Cell Carcinoma | Quercetin Chemoprevention for Squamous Cell Carcinoma in Patients With Fanconi Anemia | Quercetin administered orally twice daily at an wheight-based adjusted dosage (maximum 4000 mg/day). | |
Betulinic acid | NCT00346502/Suspended | Dysplastic Nevus Syndrome | Phase I/II Evaluation of Topical Application of 20% Betulinic Acid Ointment in the Treatment of Dysplastic Nevi With Moderate to Severe Dysplasia | Daily application of the 20% betulinic acid ointment to the dysplastic nevi site for a period of four weeks. |
Artemisimin
(Artesunate) |
NCT00764036/Completed | Breast Cancer | Prospective Open Uncontrolled Phase I Study of Compatibility, Safety&Pharmacokinetics of Artesunate, a Semisynthetic Derivative of Artemisinin From the Chinese Herb Artemisia Annua in Patients With Metastatic/Locally Advanced Breast Cancer | The administration of the drug was as follows: daily single oral doses of 100, 150 or 200 mg of artesunate, for 4 weeks. |
NCT03093129/Recruiting | Colorectal Cancer | Phase II Randomised, Double Blind, Placebo Controlled Trial of Neoadjuvant Artesunate in Stage II/III Colorectal Cancer in Vietnamese Patients | Daily administration of artesunate (200 mg) for 14 days. | |
NCT04098744/Recruiting | Cervical Neoplasia | A Phase II Double Blind, Placebo-controlled, Randomized Trial of Artesunate Vaginal Inserts for the Treatment of Patients With Cervical Intraepithelial Neoplasia (CIN2/3) | Participants will receive three 5-day cycles of artesunate inserts, 200 mg per day, at weeks 0, 2, and 4. | |
Rutin | NCT00003365/Terminated | Colon Cancer | The Effect of Plant Phenolic Compounds on Human Colon Epithelial Cells | The administration of rutin was twice a day, for 6–10 weeks. Other phytocompounds (e.g. curcumin, quercetin) were evaluated in this study as well. |
Ginseng | NCT00631852/Completed | Breast Cancer | A Phase II Biomarker Trial of Gelatin Encapsulated Extract of American Ginseng Root (LEAG) in Breast Cancer | The administration of American Ginseng Root extract was organised as follows: four 250 mg tablets daily for 5–14 days prior to surgery. |
NCT02603016/Completed | Lung Neoplasm Breast Carcinoma | Phase 1 Study of Clinical Nutrition That Research Safty and Efficacy in Lung Neoplasms And Breast Carcinoma | Two tablets of Ginseng were administered by mouth, twice a day for 42 days. |