- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06137599
GCS Survey: "GHB IN CHEMICAL SUBMISSION: MYTH OR REALITY?" (GCS)
Study Overview
Detailed Description
The Addictovigilance center of Paris (CEIP-A) has been responsible for the national chemical submission survey under the supervision of the French National Agency for the Safety of Medicines and Health Products (ANSM) since 2003, using data from expert toxicology laboratories, forensic police and forensic medicine departments. With 20 years' experience in the criminal use of substances, the center draws up an annual report on substance-facilitated assaults in order to put in place appropriate, up-to-date prevention measures.
In 2021, the #balancetonbar movement emerged in Brussels and spread like a shockwave across Belgian cities and Europe. On Instagram, women spoke out about the extent of drug-facilitated sexual assault (DFSA) in nightclubs and denounced the " laissez faire " attitude of the political authorities. The movement is resonating in France and getting louder : #balancetonbar has now been joined by #MetooGHB, which puts the so-called "rape drug" in the spotlight. But what's really going on?
A retrospective study of the national survey data from 2010 to 2019 reports only 26 chemical submissions (CS) attributable to GHB/GBL out of 617 CS identified (4.2%) among 4349 suspected cases. However, this study highlights all the limits to the disclosure of GHB (low proportion of complaints filed, speed of elimination of this substance from the usual matrices, insufficient number of court orders for hair analysis).
With the aim to eliminate the limitations identified as far as possible and answer the question "Is the massive use of GHB in chemical submission a myth or a reality?", a pilot research protocol, centred on capillary analysis, is being proposed to 200 victims in the Ile de France region.
This is a non-interventional, multi-centre, category 3 study, the only acts (hair sampling) or procedures (chemical submission declaration form) are risk-free and do not affect the management of participants.
Victims are included whether or not they have lodged a complaint, in collaboration with forensic medicine departments, HIV and STI screening Center and Victim Support Associations. Referred to the parisien CEIP-A, 3 strands of hair are sampled after an interview in which the victim's history and voluntary drug use data were taken. A pre-analytical treatment of the hair (washing, fragmentation), followed by detection by high-resolution mass spectrometry is carried out by an expert laboratory in search of GHB and other known chemical submission agents (illicit drugs and psychoactive medicines).
To meet our objective, a comparative study of the results of the GCS protocol and the survey history was carried out using an exact binomial test. This study will also provide an opportunity for a more general discussion of the value of hair analysis in the detection of chemical submission agents.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Leïla CHAOUACHI, PharmD
- Phone Number: +33 01 40 05 42 70
- Email: Leila.chaouachi@aphp.fr
Study Contact Backup
- Name: Anne Batisse, PharmD
- Phone Number: +33 01 40 05 42 65
- Email: anne.batisse@aphp.fr
Study Locations
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-
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Bondy, France, 93140
- Recruiting
- Laetitia LASNE
-
Contact:
- Laetitia LASNE, MD
-
Paris, France, 75004
- Recruiting
- Elisabeth ALCARAZ
-
Contact:
- Elisabeth ALCARAZ, MD
-
Paris, France, 75010
- Recruiting
- Leila CHAOUACHI
-
Contact:
- Leila CHAOUACHI, PharmD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Victims over the age of majority (≥ 18 years) on the day of the alleged events
- With a medical history leading to the suspicion of chemical submission:
- Presence of evocative clinical signs (amnesia and/or behavioural disorders and/or neurological disorders and/or other somatic disorders, etc.) AND
- In the presence of potential criminal acts (suspected or proven assault or attempted assault).
- French speaking
- Having been informed of the search
Exclusion Criteria:
- - Victims who were minors (<18 years) on the day of the alleged events.
- Victims who usually use GHB/GBL recreationally.
- Suspecting administration of a harmful substance with no crime or offence committed at the time and no attempted assault
- Victims of needle spiking
- Victims with very short hair (<3 cm), bald or shaven heads
- Victims who have exceeded the maximum time limit for taking a hair sample (6 months after the event)
- Do not speak French
- Oppose to participating in the study
- Victims presenting a psychotic or cognitive syndrome likely to impair judgement Victims placed under guardianship or legal protection (article L11-22-2 CSP)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evidence of exogenous GHB intake without the knowledge of the victims through hair analysis.
Time Frame: Samples taken between 2 and 6 months after the presumed events: GHB analysis in the hair can no longer be interpreted after 6 months due to the hydrosoluble nature of GHB and repetitive hair washing.
|
A double CEIP-A/Expert Laboratory interpretation is carried out according to the evaluation criteria defined by the national chemical submission survey Steering Committee.
|
Samples taken between 2 and 6 months after the presumed events: GHB analysis in the hair can no longer be interpreted after 6 months due to the hydrosoluble nature of GHB and repetitive hair washing.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evidence of the use of a psychoactive substance (other than GHB) without the knowledge of the victims via capillary analysis.
Time Frame: Samples taken between 2 and 6 months after the presumed events.
|
A double CEIP-A/Expert Laboratory interpretation is carried out according to the evaluation criteria defined by the national chemical submission survey Steering Committee.
|
Samples taken between 2 and 6 months after the presumed events.
|
Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Leïla CHAOUACHI, PharmD, APHP(ASSISTANCE PUBLIQUE DES HOPITAUX DE PARIS
- Study Director: Anne Batisse, PharmD, APHP(ASSISTANCE PUBLIQUE DES HOPITAUX DE PARIS
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- APHP230579
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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