Adaptive Decision Support for Addiction Treatment (ADAPT) Serial Randomized Testing for Usability, Round 1
NCT07549126
Chemically-Induced Disorders, Clinical Decision Support
Guilford, Connecticut, United States
View Trial DetailsNCT Number: NCT05878210
The purpose of this study is to observe and assess the successful taper and opioid withdrawal experience after participants stop receiving SUBLOCADE because their healthcare provider determines their disease symptoms have been controlled for at least 9 months and they, together with their healthcare provider, plan to discontinue MOUD.
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Notify Me18 year and older
All sexes
Observational
Savera Medical Centre, Edmonton, Alberta, Canada
This is a Phase IV, observational, multicentre, open-label, study in participants with a history of OUD, who have been on SUBLOCADE treatment for at least 12 injections, have had disease symptoms controlled for at least 9 months in the opinion of the healthcare provider, and both healthcare provider and participant plan to discontinue MOUD treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Participants must meet all of the following criteria:
Time frame: 6 months
Time frame: 6 months
Average clinical experience score (range: 0 to 4 with higher score = worse outcome) on opioid withdrawal severity during the past month
Time frame: 6 months
Yes/No
Time frame: 6 months
Yes/No
Time frame: 6 months
Yes/No
Time frame: 6 months
Yes/No
Time frame: 6 months
Yes/No
Indivior Inc.
Industry
A Phase IV Study to Evaluate the SUBLOCADE Treatment Exit Strategy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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