Status: Not yet recruiting
Evaluation of the Efficacy of QUITOXIL® in Smoking Cessation
As part of post-marketing clinical monitoring and with a view to applying for the digital medical device Quitoxil® to be included on the LPPR list, this prospective, multicentre, controlled, randomised clinical trial aims to evaluate the clinical impact of support provided by Quitoxil® as an adjunct to conventional management for patients undergoing smoking cessation who have a tobacco use disorder.
Participants needed: 606
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: KLAVA InnovationUpdated: Jul 24, 2026
Eligibility criteria
Men or women aged between 18 and 65 [+10]
Individuals who, at the time of inclusion ( ), have been receiving another form... [+6]