Evaluation of an Opioid Decrease Strategy in Chronic (EODSCPP)
Evaluation of an Opioid Decrease Strategy in Chronic Pain Patients at the Pain Assessment and Treatment Center in Montpellier: Prospective Study Over 6 Months.
Increase in the consumption of analgesics observed in many countries with a mediatic crisis resulting in an increasingly frequent wish of patients to wean themselves from opiates. A recent update (B. Rolland 2017) suggests that upon initiation of an opioid analgesic treatment, the patient should be informed of the risk of opioid dependence and misuse. There is no clearly validated decay scheme in the event of dependence in patients with Chronic Non-Cancer Pain.
Hypotheses:
- Possibility of a rapid decrease in opioid analgesic treatments at DCNC sensitized to the risk of DOP and MOP. (Protocol implemented: Multidisciplinary assessment, workshops and information sheet on chronic pain, treatments and risk of DOP, pharmacological and nonpharmacological adaptation)
- Highlight the need for additional information from patients and prescribers on the risk of DOP and MOP in DCNC.
Studieöversikt
Detaljerad beskrivning
Main objective: Check if the rapid to semi-rapid regimen (- 25 to -60% dosage in 5 days of HDS) of opioid analgesics, without the use of methadone or buprenorphine agonists, in the case of DCNC at the CETD in Montpellier is efficient in the medium term (6 months).
Secondary objective:
- With our inclusion questionnaire we wanted to check if the patients had been made aware of the risk of opiate dependence and misuse.
- Detect the conditions of prescriptions that can promote the misuse of opiates.
- Evaluating the different components of residual pain at 6 months (type, intensity, anxiety component and depression, function).
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
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Montpellier, Frankrike, 34295
- Uhmontpellier
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Inclusion criteria:
- chronic pain patient
- major
- supported at CETD
Exclusion criteria:
-patient with physical and mental incapacity to participate in the study
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
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Patients included from 10/01/19 to 12/31/19.
Patients included from 10/01/19 to 12/31/19.
(the study will be extended to a larger number of patients according to the first results), continued according to the first results.
DCNC patients treated at the Montpellier Pain Assessment and Treatment Center hospitalized during the period from 10/01/19 to 12/31/19, for misuse of opioid treatment.
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The data retrieved from the patient will be encrypted and there will also be written data or written in binary form.
They will be used to create an Excel table which allows me to list the data on D1 then on M + 3 then on M + 6 in order to evaluate the evolution of these data over a time interval of 6 months and this is which will be used as support in my thesis in pharmacy.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
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Change of the dosage of opioid and co-analgesic treatments
Tidsram: 3 months and 6 months
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Change of the dosage of opioid and co-analgesic treatments
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3 months and 6 months
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
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Measuring quality of life
Tidsram: Inclusion, 3 and 6 months
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interview with the patient
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Inclusion, 3 and 6 months
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Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Théa GENDARME, MD, PharmD, MSc, Uh Montpellier
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- RECHMPL20_0132
Plan för individuella deltagardata (IPD)
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