Evidence map›Paper›PMID 31103778›Full record

ArticleThe International journal on drug policy2019

Kratom policy: The challenge of balancing therapeutic potential with public safety.

Walter C Prozialeck, Bonnie A Avery, Edward W Boyer, Oliver Grundmann, Jack E Henningfield, Andrew C Kruegel, Lance R McMahon, Christopher R McCurdy, Marc T Swogger, Charles A Veltri and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The International journal on drug policy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
13.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 102 citations in OpenAlex.

  1. The effects of kratomFrontiers in pharmacology · 2025
    Pooled it
  2. Pooled it
  3. Trial
  4. Observational
  5. Kratom (Molecules (Basel, Switzerland) · 2026
    Article
  6. Kratom Brands in Vape Shops Across the US.Health behavior research · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Translating Kratom-Drug Interactions: From Bedside to Bench and Back.Drug metabolism and disposition: the biological fate of chemicals · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 2 countries.

Walter C ProzialeckDepartment of Pharmacology, Midwestern University, 555 31st Street, Downers Grove, IL 60515, USA. Electronic address: wprozi@midwestern.edu.
Bonnie A AveryDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA.
Edward W BoyerDepartment of Emergency Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. Electronic address: edward.boyer@childrens.harvard.edu.
Oliver GrundmannDepartment of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA. Electronic address: grundman@ufl.edu.
Jack E HenningfieldResearch, Health Policy and Abuse, Liability, Pinney Associates And Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, 4800 Montgomery Lane, Suite 400, Bethesda, MD 20814, USA. Electronic address: jhenning@pinneyassociates.com.
Andrew C KruegelDepartment of Chemistry, Columbia University, 3000 Broadway, New York, NY 10027, USA. Electronic address: ack2137@columbia.edu.
Lance R McMahonDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA. Electronic address: lance.mcmahon@cop.ufl.edu.
Christopher R McCurdyDepartment of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA. Electronic address: cmccurdy@cop.ufl.edu.
Marc T SwoggerDepartment of Psychiatry, University of Rochester Medical Center, 300 Crittenden Blvd., Rochester, NY 14682, USA. Electronic address: marc_swogger@urmc.rochester.edu.
Charles A VeltriDepartment of Pharmaceutical Sciences, Midwestern University, 19555 N. 59th Avenue, Glendale, AZ 85308, USA. Electronic address: cveltr@midwestern.edu.
Darshan SinghCentre for Drug Research, Universiti Sains Malaysia, Minden, Malaysia. Electronic address: darshan@usm.my.
University of Florida · USMidwestern University · USBrigham and Women's Hospital · USColumbia University · USJohns Hopkins University · USUniversiti Sains Malaysia · MYUniversity of Rochester Medical Center · US

Funding

Opioid use disorders: UF Pharmacy medications discovery and developmentUG3DA048353 · NIDA · UNIVERSITY OF FLORIDA · PI MCCURDY, CHRISTOPHER R, MCMAHON, LANCE R. · 2019 to 2020
$3.6M
Kratom alkaloids: in vitro and in vivo pharmacological mechanismsR01DA047855 · NIDA · UNIVERSITY OF FLORIDA · PI MCCURDY, CHRISTOPHER R, MCMAHON, LANCE R. · 2019 to 2023
$3.6M
Mentoring in Advanced mHealth Technologies and Machine Learning for HIV/Drug Abuse ResearchK24DA037109 · NIDA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BOYER, EDWARD W · 2014 to 2025
$1.9M
NIDA NIH HHS K24 DA037109NIDA NIH HHS R01 DA047855NIDA NIH HHS UG3 DA048353
6 · The paper itself

Abstract

Kratom (Mitragyna speciosa) is a tree-like plant indigenous to Southeast Asia. Its leaves, and the teas brewed from them have long been used by people in that region to stave off fatigue and to manage pain and opioid withdrawal. Evidence suggests kratom is being increasingly used by people in the United States and Europe for the self-management of opioid withdrawal and treatment of pain. Recent studies have confirmed that kratom and its chemical constituents have potentially useful pharmacological actions. However, there have also been increasing numbers of reports of adverse effects resulting from use of kratom products. In August 2016, the US Drug Enforcement Administration announced plans to classify kratom and its mitragynine constituents as Schedule I Controlled Substances, a move that triggered a massive response from pro-kratom advocates. The debate regarding the risks, and benefits and safety of kratom continues to intensify. Kratom proponents tout kratom as a safer and less addictive alternative to opioids for the management of pain and opioid addiction. The anti-kratom faction argues that kratom, itself, is a dangerous and addictive drug that ought to be banned. Given the widespread use of kratom and the extensive media attention it is receiving, it is important for physicians, scientists and policy makers to be knowledgeable about the subject. The purpose of this commentary is to update readers about recent developments and controversies in this rapidly evolving area. All of the authors are engaged in various aspects of kratom research and it is our intention to provide a fair and balanced overview that can form the basis for informed decisions on kratom policy. Our conclusions from these analyses are: (a) User reports and results of preclinical studies in animals strongly suggest that kratom and its main constituent alkaloid, mitragynine may have useful activity in alleviating pain and managing symptoms of opioid withdrawal, even though well-controlled clinical trials have yet to be done. (b) Even though kratom lacks many of the toxicities of classic opioids, there are legitimate concerns about the safety and lack of quality control of purported "kratom" products that are being sold in the US. (c) The issues regarding the safety and efficacy of kratom and its mitragynine constituent can only be resolved by additional research. Classification of the Mitragyna alkaloids as Schedule I controlled substances would substantially impede this important research on kratom.

Indexed as

AnimalsDrug and Narcotic ControlHumansMitragynaPlant ExtractsPlant LeavesSecologanin Tryptamine AlkaloidsSubstance Withdrawal SyndromemitragyninePlant ExtractsSecologanin Tryptamine AlkaloidsDrug policyKetumKratomMitragynineOpioid use disorder (OUD)Pain management

Identifiers

PMID31103778
PMCPMC7881941
OpenAlexW2946482102

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.