Stomach Ulcers Research Dashboard
Double-blind human trials
Clinical human trials
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As a subscriber, you will be able to access dashboard insights including chemotype overviews and dosing summaries for medical conditions and organ system and receptor breakdowns for cannabinoid and terpene searches. Study lists present important guidance including dosing and chemotype information with the ability to drill down to the published material. And all outputs are fully filterable, to help find just the information you need. Stay up-to-date with the science of cannabis and the endocannabinoid system with CannaKeys.
CannaKeys has 18 studies associated with Stomach Ulcers.
Here is a small sampling of Stomach Ulcers studies by title:
- Ameliorative effects of ribes rubrum oil against gastric ulcers caused by indomethacin in experimental models
- MAGL inhibition modulates gastric secretion and motility following NSAID exposure in mice
- Gastric acid inhibitory and gastric protective effects of Cannabis and cannabinoids.
- Gastroprotective Effect of Alpha-Pinene and Its Correlation With Antiulcerogenic Activity of Essential Oils Obtained From Hyptis Species
- The effect of a minor constituent of essential oil from Citrus aurantium: the role of β-myrcene in preventing peptic ulcer disease.
Components of the Stomach Ulcers Research Dashboard
- Dosing information available for Stomach Ulcers
- Chemotype guidance for treating Stomach Ulcers with cannabis
- Synopsis of cannabis research for Stomach Ulcers
- Individual study details for Stomach Ulcers
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Members can filter by the following criteria:
- Study Type
- Cannabinoids & Endocannabinoids
- Study Result
- Year of Publication
Overview - Stomach Ulcers
Description of Stomach Ulcers
The stomach is lined with a thick mucus membrane protecting it from the acidic digestive juices. When the mucus membranes break or thin enough for the acid to burn the underlying tissue ulcer form. Common culprits have been identified and include the over-use of NSAIDs, bacterial infection (Helicobacter pylori), tobacco, alcohol, chronic and severe stress for example. Orthodox treatments depend on underlying causes and severity and as such may include life-style changes (e.g. smoking or alcohol cessation), antibiotics, or surgery for instance.
Diseases of the Digestive System
ICD-10 Code: K25
Stomach Ulcers Symptoms:
Center/upper abdominal pain especially lying down, burning sensation in stomach, vomiting blood (red or coffee ground emesis), black stool
Also known as:
Peptic Ulcer, Gastric Ulcer, Pylorus ulcer
THC Interaction with Pharmaceutical Drugs
- THC can enhance the effects of drugs that cause sedation and depress the central nervous system, such as benzodiazepines, barbiturates, and alcohol, for example.
- THC is metabolized by and an inhibitor of a number of enzymatic liver pathways referred to as cytochrome P450. There are more than 50 enzymes belonging to this enzyme family, a number of which are responsible for the breakdown of common drugs such as antidepressants (e.g. amitriptyline, doxepine, fluvoxamine), antipsychotics (haloperidol, clozapine, stelazine), beta-blockers (e.g. propranolol), bronchodilators (e.g. theophylline), or bloodthinners (e.g. warfarin). Thus patients taking these classes of medication may find that THC increases the concentration and effects of these drugs as well as the duration of their effects.
- Clinical observation suggests no likely interactions with other pharmaceuticals at a total daily dose of up to 20mg THC.
CBD Interaction with Pharmaceutical Drugs
- CBD may alter action on metabolic enzymes (certain drug-transport mechanisms), and as such may alter interactions with other drugs, some of which may produce therapeutic or adverse effects. For instance, CBD interacts with the enzyme cytochrome P450 3A4 and cytochrome P450 2C19, increasing the bioavailability of anti-epileptic drugs such as clobazam (a benzodiazepine). This makes it possible to achieve the same results at significantly lower dosages, reducing treatment costs and risks of adverse effects.
- Groups of drugs affected include: anti-epileptic drugs, psychiatric drugs, and drugs affecting metabolic enzymes, for example.
- Clinical observations suggest no likely interactions with other pharmaceuticals at a total daily dose of up to 100mg CBD
THC Dosage Considerations
- THC micro dose: 0.1 mg to 0.4 mg
- THC low dose: 0.5 mg to 5 mg
- THC medium dose: 6 mg to 20 mg
- THC high dose: 21 mg to 50+ mg
CBD Dosage Considerations
- CBD low dose: 0.4 mg to 19 mg
- CBD medium dose: 20 mg to 99 mg
- CBD high dose: 100 mg to 800+ mg (upper limits tested ~1,500mg)
Disclaimers: Information on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for diagnosing a health problem or disease. If using a product, you should read carefully all product packaging. If you have or suspect that you have a medical problem, promptly contact your health care provider.
Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.