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Clinical Trials in Canada / NCT05883358
Recruiting Observational

Kratom Use Disorder Management Using Clonidine and/or Buprenorphine

NCT05883358 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2018-07-02
Last updated
2025-01-27

Condition(s) studied

Withdrawal Syndrome

Investigational drug(s) / intervention(s)

Clonidine, Buprenorphine →

Clonidine, Buprenorphine: Each patient receives rotational treatment using Buprenorphine 5cmg/hr patch; or Clonidine tablet 0.1mg 4hourly; or combined Clonidine tablet 0.1mg 4hourly + Buprenorphine 5cmg/hr patch.

Study summary

Kratom is used for stimulant, analgesic, anxiolytic, and sedative effects. There is inadequate knowledge about Kratom addiction. Kratom withdrawal may be treated like opioid withdrawal.

Prospective observational crossover study of consenting adults who are undergoing Kratom withdrawal management. On alternate weeks, each patient receives treatment using Buprenorphine 5cmg/hr patch; or Clonidine tablet 0.1mg 4hourly; or combined Clonidine tablet 0.1mg 4hourly + Buprenorphine 5cmg/hr patch. Each patient will undergo treatment for 12 weeks.

Patients will use Subjective Opiate Withdrawal Scale (SOWS) to collect data on daily basis. SOWS is a patient-administered tool that is used to record the severity and presence of opiate withdrawal. The physician will also use Clinical Opiate Withdrawal Scale (COWS) to collect data on weekly basis. COWS is a clinician-administered tool that is used to record the signs of opiate withdrawal. A change in the COWS and SOWS scores by 6-points is considered significant.

Eligibility

Sex
ALL
Min age
20 Years
Max age
99 Years
Healthy volunteers
Accepted
Inclusion Criteria: * adult patients * Kratom dependence * Kratom withdrawal syndrome * Kratom withdrawal therapy * good treatment compliance * reliable Subjective Opiate Withdrawal Scale (SOWS) diary * reliable Clinical Opiate Withdrawal Scale (COWS) diary * informed consent for diary review * consent for clinical record quality assurance review Exclusion Criteria: * poor treatment compliance * cognitive disorder * inability to provide consent * major neuropsychiatric disorder * unreliable diary * cannabis use * excessive alcohol intake * previous adverse/allergic reactions to clonidine * previous adverse/allergic reactions to buprenorphine

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Salem Anaesthesia Pain Clinic Surrey British Columbia Recruiting

More Salem Anaesthesia Pain Clinic trials in Canada

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05883358 on ClinicalTrials.gov ↗ ← All trials in Canada