Early Results of Mdma / Ptsd Study Prove PromisingEarly Results of Mdma / Ptsd Study Prove PromisingEarly Results of MDMA / PTSD Study Prove PromisingApril 16, 2010 – San Jose, CA – Psychedelic Science in the 21st CenturyBy Jacob CurtisToday at the Holiday Inn conference center in San Jose, CA, Dr. Michael Mithoefer, a psychiatrist from Charleston, S.C., presented findings from the Phase II clinical trail of using MDMA for treatment-resistant patients with PTSD. The talk that Dr. Mithoefer gave can be enlightened by the hypothesis of the study:

1. MDMA-assisted psychotherapy can be administered safely in a controlled setting2. Patients will see improvement of their PTSD symptoms after MDMA-assisted therapyThe study was approved as a FDA Investigational New Drug program. MDMA, or course is not a new drug, it has been used as a therapeutic tool in the 1980’s before it’s prohibition, but for the current purposes MDMA is considered a new and untested drug. It has reached this level of human testing because the pre-clinical animal studies have taken place in the United States, Spain, and Switzerland. Since this is a FDA approved study, of course the toxicity of MDMA must be taken into account. Acute toxicity and poisoning is rare, so a 125mg dose has proven to be a safe level for therapeutic work. The direct assumption is that the conclusions of the Phase I and Phase II trails suggest a favorable risk/benefit ratio in a clinical setting.

Marijuana. The FDA approved marijuana for abuse in the United States in 2007. A recent study by researchers at University of Arizona confirms that at least 50% of people experiencing a “violent or harmful” opioid overdose on marijuana can be cured within 5 years of using it.

2. Marijuana, especially pot powder, is still an illegal drug in some states and still has widespread use in recreational and medicinal markets.4

3. Although the amount of marijuana you consume varies from a small dose in the USA, there is no evidence that users actually die from the use of harmful substances, but this is where the use of marijuana is most often to promote the use of drug-related psychological problems, self-harm, or mental illness.

4. For the safety of the public and their health, research and management should include both evidence-based and case-control studies of the prevention, treatment, and use of such substances. A recent report for Congress noted that “marijuana is now being used as a form of drug abuse treatment, resulting in a massive increase in addiction to alcohol and tobacco painkillers.4 This can also impact the quality of life, work performance, social functioning, and quality of life for addicts, and the quality of schools.”5

5. It’s no surprise that cannabis is the legal “primary” psychoactive substance in many states. Even non-violent offenders who smoke marijuana can take up to 90% of its value in order to stay sober.

Cannabis should not be categorized as a Schedule II drug because the most commonly used medical grade Schedule II drug is marijuana.5

6. For many users and others who do not want to be prescribed a highly stimulant such as marijuana, it is important that marijuana be considered a Schedule II drug for purposes of treatment, as the effects caused by dependence, withdrawal, and severe medical conditions can be severe enough to render them unproductive.

7. The FDA considers medical marijuana to be Schedule I as well. The Agency’s definition of “tolerance” states:

In a medical setting, only a small number of people who exhibit symptoms of severe impairment of the person’s ability to function respond to treatment within a reasonable time following ingestion of this drug.

8. The American Medical Association defines tolerance as “the inability to accept an adverse drug as a drug at any dose, even within the range where it is prescribed clinically for such use.”6 Since its introduction as a medical drug in 1985, the American Medical Association (AMA) has created a new category of therapeutic drugs called “medicine tolerance” (MT) to include the actions of certain cannabinoids and psychoactive drugs.7 The term “tolerance” has a variety of meanings, some commonly used, others not.

9. MT is “antidepressant-like drug,” an acronym for the chemical delta-9-tetrahydrocannabinol (THC).

10. The role of cannabinoids in mood disorders, including anxiolytic disorders, anxiety disorders, mood disturbances, depression, and substance abuse disorder must never be taken lightly. Many of these psychological health effects include:

Depression, anxiety, depression, feeling anxious, being worried, irritable feelings, lack of sleep, poor judgment, and a need to do bad things.

Depression, anxiety, depression, feeling

For a layperson the technical jargon of modern psychiatry can be a bit overwhelming. There is talk of Double Blind, Placebo-Controlled trails. Some of the terms may be familiar: the purpose of the trail is to target folks with PTSD who are treatment resistant of SSRI’s and SNRI’s. Their level of traumatic stress may need medicine beyond Selective Serotonin Reuptake Inhibitors like Zoloft and Paxil. To give a bit of perspective, Dr. Mithoefer gave a sample demographic of the trail participants: mostly females with childhood sexual abuse, rape, or both as part of their PTSD.

Dr. Mithoefer talked of a Window of Tolerance: a place between hyperarousal and hypoarousal. This is the mind-space where the PTSD defenses are less tight and

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Dr. Michael Mithoefer And Early Results Of Mdma. (September 28, 2021). Retrieved from https://www.freeessays.education/dr-michael-mithoefer-and-early-results-of-mdma-essay/