search
Back to results

Pregabalin for Opiate Withdrawal Syndrome

Primary Purpose

Opioid Withdrawal

Status
Completed
Phase
Phase 4
Locations
Russian Federation
Study Type
Interventional
Intervention
Pregabalin
Clonidine
Doxylamin
Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine)
Sponsored by
St. Petersburg Bekhterev Research Psychoneurological Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Withdrawal

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Opioid Use Disorders; Opioid Withdrawal Syndrome

Exclusion Criteria:

  • Severe psychiatric and somatic disorders, other Substance Use Disorders (except tobacco)

Sites / Locations

  • St.-Petersburg Bekhterev Reserach Psychoneurological Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Pregabalin

Clonidine

Arm Description

This group (N= 40) receives up to 600 mg a day of Pregabalin for six-seven days along with symptomatic therapy that is divided into basic treatment that is given to all patients (Doxylamin 30 mg/day) and additional medications based on patients' needs as determined by a psychiatrist using the Opioid Withdrawal Scale and included Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine).

This group (N= 40) receives up to 600 micrograms of Clonidine a day for six-seven days along with symptomatic therapy that is divided into basic treatment that is given to all patients (Doxylamin 30 mg/day) and additional medications based on patients' needs as determined by a psychiatrist using the Opioid Withdrawal Scale and included Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine)..

Outcomes

Primary Outcome Measures

Number of patients completed detoxification
Compares number of patients that finish treatment of opioid withdrawal syndrome (detoxification) in two treatment arms.

Secondary Outcome Measures

Severity of opiod withdrawal
Compares changes of severity of opioid withdrawal syndrome in two arms
Amount of Ketorolac administered
Compares amount of Ketorolac administered under the symptom triggered protocol (per patient's request of physician's judgement) in two arms.
Number and severity of adverse events
Compares number and severity of adverse events in two treatment arms

Full Information

First Posted
January 6, 2017
Last Updated
April 4, 2020
Sponsor
St. Petersburg Bekhterev Research Psychoneurological Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT03017430
Brief Title
Pregabalin for Opiate Withdrawal Syndrome
Official Title
Randomized Clinical Trial of Pregabalin for Opioid Withdrawal Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
January 2014 (Actual)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Petersburg Bekhterev Research Psychoneurological Institute

4. Oversight

5. Study Description

Brief Summary
It is a single blind randomized symptom triggered study to assess efficacy and safety of pregablin combined with the symptom triggered treatment for opiate withdrawal syndrome vs. clonidne with the same with the symptom triggered treatment for opiate withdrawal syndrome.
Detailed Description
Study design: Single-blind randomized symptom-regulated protocol with an active control. Eighty patients admitted to an inpatient addiction treatment program will be randomly assigned to two groups. The first group (N=40) receives up to 600 mg a day of Pregabalin for six days along with symptomatic therapy that is divided into basic treatment that is given to all patients (Doxylamin 30 mg/day) and additional medications based on patients' needs as determined by a psychiatrist using the Opioid Withdrawal Scale and included Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine). The second group (N= 40) receives up to 600 micrograms of Clonidine a day as the main treatment along with the same basic and symptomatic regimen. Opiate withdrawal severity, craving, sleep disturbance, anxiety and depression, as well as general clinical impressions and side effects are assessed daily by psychiatrists who are blind to patients' group assignment using internationally validated quantitative psychometric instruments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Withdrawal

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pregabalin
Arm Type
Experimental
Arm Description
This group (N= 40) receives up to 600 mg a day of Pregabalin for six-seven days along with symptomatic therapy that is divided into basic treatment that is given to all patients (Doxylamin 30 mg/day) and additional medications based on patients' needs as determined by a psychiatrist using the Opioid Withdrawal Scale and included Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine).
Arm Title
Clonidine
Arm Type
Active Comparator
Arm Description
This group (N= 40) receives up to 600 micrograms of Clonidine a day for six-seven days along with symptomatic therapy that is divided into basic treatment that is given to all patients (Doxylamin 30 mg/day) and additional medications based on patients' needs as determined by a psychiatrist using the Opioid Withdrawal Scale and included Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine)..
Intervention Type
Drug
Intervention Name(s)
Pregabalin
Intervention Description
Pregabalin 600 mg a day for six-seven days along with symptomatic therapy: Doxylamin 30 mg/day, Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine).
Intervention Type
Drug
Intervention Name(s)
Clonidine
Intervention Description
Clonidine 600 micrograms a day for six-seven days along with symptomatic therapy: Doxylamin 30 mg/day, Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine)
Intervention Type
Drug
Intervention Name(s)
Doxylamin
Intervention Type
Drug
Intervention Name(s)
Ketorolac, Loperamide, Metoclopramide, Nefazolin and Phenazepam (benzodiazepine)
Primary Outcome Measure Information:
Title
Number of patients completed detoxification
Description
Compares number of patients that finish treatment of opioid withdrawal syndrome (detoxification) in two treatment arms.
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Severity of opiod withdrawal
Description
Compares changes of severity of opioid withdrawal syndrome in two arms
Time Frame
7 days
Title
Amount of Ketorolac administered
Description
Compares amount of Ketorolac administered under the symptom triggered protocol (per patient's request of physician's judgement) in two arms.
Time Frame
7 days
Title
Number and severity of adverse events
Description
Compares number and severity of adverse events in two treatment arms
Time Frame
7 days
Other Pre-specified Outcome Measures:
Title
Craving for opiates
Description
Craving for opiates will be measured with the visual analog scale. Compares craving for opiates in two treatment arms during detoxification.
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Opioid Use Disorders; Opioid Withdrawal Syndrome Exclusion Criteria: Severe psychiatric and somatic disorders, other Substance Use Disorders (except tobacco)
Facility Information:
Facility Name
St.-Petersburg Bekhterev Reserach Psychoneurological Institute
City
St.-Petersburg
ZIP/Postal Code
192019
Country
Russian Federation

12. IPD Sharing Statement

Learn more about this trial

Pregabalin for Opiate Withdrawal Syndrome

We'll reach out to this number within 24 hrs