SAMBA: Advanced Nurses vs. General Practitioners for the Management of Outpatient Alcohol Detox: a Safety and Cost Comparison

Sponsor
University Hospital, Lille (Other)
Overall Status
Terminated
CT.gov ID
NCT03056365
Collaborator
Ministry of Health, France (Other)
73
26
2
49
2.8
0.1

Study Details

Study Description

Brief Summary

The SAMBA study aims to assess the safety and cost comparison of the management of outpatient alcohol detoxification, between an advanced nurse protocol on the one hand (experimental group), and a GP-based treatment on the other hand (standard-of-care group).

In the advanced nurse (AN) group, nurses manage alcohol detox using a predefined protocol based on both the Cushman and CIWA-Ar scales. Depending on the Cushman and CIWA-Ar scores, which are calculated at every consultation, advanced nurse can adjust the diazepam dosing. In case of any serious adverse event or uncontrolled withdrawal complication, an addiction specialist stands in back-up and can be appealed to decide whether the outpatient detox can be continued or whether the patient has to be hospitalized. In the GP group, GPs can manage patients as they wish.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Advanced Nurse (AN)
  • Procedure: General Practitioner (GP)
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
73 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Advanced Nurses vs. General Practitioners for the Management of Outpatient Alcohol Detoxification: a Randomized Clinical Trial Comparing Safety and Costs
Actual Study Start Date :
Jan 1, 2017
Actual Primary Completion Date :
Feb 1, 2021
Actual Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Advanced Nurse (AN)

The outpatient detoxication procedure will be entirely managed by an advanced nurse team, using a predefined protocol decision algorithm. The protocol allows that the AN team autonomously manages the diazepam dosing during the detox period. Addiction physicians only intervenes in case of severe withdrawal symptoms or serious adverse events.

Procedure: Advanced Nurse (AN)
Protocoled AN-based management of detox

Active Comparator: General Practitioner (GP)

The outpatient detoxication procedure is entrusted to a GP who will manage patients and diazepam dosing as he/she thinks best ("as usual" control group)

Procedure: General Practitioner (GP)
'As usual' medical management of detox

Outcome Measures

Primary Outcome Measures

  1. Number of patients considered in failure of outpatient alcohol detoxification period [15 days]

    Hospitalization required (any cause) across the 15 days following the detox start

Secondary Outcome Measures

  1. The total costs for each arm by cost-minimization [during the 15 days of the outpatient alcohol detoxification]

    All medical costs (visits, medications, hospitalizations, ambulance,..) resulting from the detoxification management

  2. Number of patients reporting at least one recovery in alcohol consumption [during the 15 days of the outpatient alcohol detoxification]

    alcohol consumption obtained from A-TLFB data

  3. Number of patients reporting at least one high alcohol intake [during the 15 days of the outpatient alcohol detoxification]

    High alcohol intake defined by consumption of more than 5 standard drinks per day

  4. Number of patients with adverse events [during the 15 days of the outpatient alcohol detoxification]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • DSM-IV-Tr criteria for alcohol dependence

  • Clinical indication for alcohol detoxification

  • Social Insurance

  • Signed Consent Form for participation

Exclusion Criteria:
  • Previous history of seizures

  • previous history of delirium tremens

  • acute or chronic liver failure

  • contraindication for using diazepam

  • average daily alcohol use of 300g of ethanol

  • SADQ score of 30 or more

  • chronic treatment with baclofen or disulfiram

  • current DMS-IV-Tr criteria for major depressive episode, or lifelong history of bipolar or psychotic disorder

  • any physical, cognitive, or psychiatric disorder that expose the subjects to enhanced risks (at the discretion of the investigator)

  • previous participation in the SAMBA study

  • social isolation of homelessness (at the discretion of the investigator)

  • pregnancy or breastfeeding

  • guardianship or curatorship

  • previous participation in a biomedical study over the previous month

Contacts and Locations

Locations

Site City State Country Postal Code
1 CH Beziers Beziers France
2 CH Boulogne Boulogne France
3 CHU Brest Brest France
4 CHU Clermont-Ferrand Clermont Ferrand France
5 Csapa Anpaa63 Clermont Ferrand France
6 CHU Créteil Creteil France
7 CH Dunkerque Dunkerque France
8 CHU Grenoble Grenoble France
9 CH Lens - CSAPA Le Square Lens France
10 CSAPA CHRU - Le PARI Lille France
11 CH Limoux Limoux France
12 CSAPA Arc-en-Ciel Montpellier France
13 CHU Nancy Nancy France
14 CHU Nantes Nantes France
15 Les Apsyades Nantes France
16 Centre LOGOS Nimes France
17 CH Perpignan Perpignan France
18 Csapa Anpaa66 Perpignan France
19 CH Roubaix Roubaix France
20 CSAPA La Trame - ANPAA59 Roubaix France
21 CHU Rouen Rouen France
22 CH du Rouvray Rouvray France
23 CH Alpes-Isère Saint-Egrève France
24 CHU Strasbourg Strasbourg France
25 CH Tourcoing Tourcoing France
26 CH Troyes Troyes France

Sponsors and Collaborators

  • University Hospital, Lille
  • Ministry of Health, France

Investigators

  • Principal Investigator: Renaud JARDRI, MD, PhD, University Hospital, Lille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Lille
ClinicalTrials.gov Identifier:
NCT03056365
Other Study ID Numbers:
  • 2015_09
  • 2015-A01936-43
  • PREPS_14-0209
First Posted:
Feb 17, 2017
Last Update Posted:
Jul 12, 2022
Last Verified:
Feb 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Lille
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 12, 2022