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The Comparison of Stress Response to Rapid Opioid Detoxification Applying Different Methods of Opioid Antagonism

V

Vilnius University

Status

Completed

Conditions

Opiate Addiction

Treatments

Drug: Naltrexone
Drug: Clonidine
Drug: Lorazepam

Study type

Interventional

Funder types

Other

Identifiers

NCT02362256
158200-01-443-124

Details and patient eligibility

About

The aim of this study is to investigate which method of naltrexone induction during rapid opioid detoxification causes stronger stress response and has a higher influence on opioid abstinence caused by opioid induction.

Full description

Study enrolls opiate addicted patients who are motivated for a long term treatment and full opiate abstinence. Patient is offered to take part in a study. Information is provided regarding protocol, aim and course of study. Patients who are eligible and consent for study commit to follow the pre-study recommendations.

Study consists of:

Primary assessment - information about study. Assessment of patient according to predefined criteria. Consent form. Allocation of the treatment date.

Stabilization - Buprenorphine. Assessment according to SOWS and OWS. Total amount of buprenorphine is recorded.

Repeated evaluation - patient after successful stabilization course undergoes urine test for psychotropic substances, blood alcohol level is recorded. If any test is positive patient is not enrolled to study.

Correction of opioid withdrawal symptoms - all of the patients receive medicines for opioid detoxification, infusion therapy in predefined doses.

Antagonist induction - patients receive opioid antagonist (incremental or standard dose). Withdrawal symptoms are assessed and correction with lorazepam is given if needed.

Data collection - data is recorded (demographic, epidemiological, vital signs, opioid withdrawal symptoms, levels of hormones, metabolites, electrolytes).

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Opiate addiction
  • Use of short-acting opiate (morphine or heroine)
  • Age > 18 years
  • Length of opiate addiction > 1 year
  • Patient can make a decision for detoxification and has a capacity to consent for procedure
  • Written consent for procedure

Exclusion criteria

  • Polyvalent addiction
  • Pregnancy or breast feeding
  • Cardiovascular pathology
  • Acute or chronic kidney disease
  • Decompensated liver pathology (jaundice, ascites, hepatic encephalopathy)
  • Infective complications of opiate addiction (pneumonia, phlegmon, abscess, thombophlebitis, sepsis)
  • Malnutrition (Nutritional risk screening 2002 score ≥3)
  • Diabetes mellitus
  • Previous history of psychosis
  • Glasgow coma scale < 15
  • Abdominal surgical intervention during last 30 days
  • Cumulative buprenorphine dose for stabilization < 8 mg
  • Positive test for psychoactive substances during treatment
  • Refusal to participate in study at any point of it

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

Intervention
Experimental group
Description:
Opioid antagonist induction. Day 4. Duration 12-16 hours. Naltrexone gradual increase from 50 µg p/o to a total dose of 12,5 mg according to a predefined protocol: 1. st hour 50 µg 2. nd hour 50 µg 3. rd hour 100 µg 4. th hour 100 µg 5. th hour 200 µg 6. th hour 400 µg 7. th hour 800 µg 8. th hour 1600 µg 9. th hour 3200 µg 10. th hour 6000 µg Correction of symptoms for opioid abstinence: Clonidine 150 µg p/o every 4 hours (Day 3 and Day 4) Lorazepam 5 mg p/o every 4 hours (Day 3 and Day 4), Lorazepam 2,5 mg po every 4 hours (Day 5, Day 6)
Treatment:
Drug: Lorazepam
Drug: Clonidine
Drug: Naltrexone
Control
Active Comparator group
Description:
Opioid antagonist induction. Day 4. Duration 12-16 hours. Naltrexone single dose 12,5 mg p/o Correction of symptoms for opioid abstinence: Clonidine 150 µg p/o every 4 hours (Day 3 and Day 4) Lorazepam 5 mg p/o every 4 hours (Day 3 and Day 4), Lorazepam 2,5 mg po every 4 hours (Day 5, Day 6)
Treatment:
Drug: Lorazepam
Drug: Clonidine
Drug: Naltrexone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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