← Back to Clinical Trials
Recruiting Phase 4 NCT06254001

NCT06254001 Effectiveness of Combined Tobacco Treatment in Hospitalized Subjects

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06254001
Status Recruiting
Phase Phase 4
Sponsor National Institute of Respiratory Diseases, Mexico
Condition Tobacco Smoking
Study Type INTERVENTIONAL
Enrollment 134 participants
Start Date 2024-01-15
Primary Completion 2025-01-15

Trial Parameters

Condition Tobacco Smoking
Sponsor National Institute of Respiratory Diseases, Mexico
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 134
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-01-15
Completion 2025-01-15
Interventions
BupropionNicotine replacement therapy (Nicotine patches)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

In the 20th century, tobacco caused the death of 100 million people worldwide and it is estimated that it will be responsible for 1 billion deaths in the 21st century. Currently 8 million people die each year from smoking, 7 million are associated with active smoking, thus being the main risk factor for loss of disability-adjusted life years for men and the ninth most important risk factor for women. In previous studies it has been reported that approximately 21% (14%-30%) of subjects who have required hospitalization are active smokers, being higher in men than in women (28% vs 14%). The initiation of treatment for smoking cessation in this group of subjects has shown an effectiveness rate of up to 65% to maintain abstinence 6 to 12 months after discharge. The effectiveness has been analyzed in scenarios with only brief advice, in some others with the use of medications such as varenicline, bupropion and nicotine replacement therapy, however, the interventions have not been standardized for adequate analysis, which could contribute to the different results.

Eligibility Criteria

Inclusion Criteria: \>18 years Active smokers (consumption of more than 100 cigarettes in their entire life, and who have consumed cigarettes in the last 30 days) Hospitalized subjects Informed consent Exclusion Criteria: * Subjects who have had pharmacological treatment to stop smoking in the last month * Subjects with contraindications for medications. Sample size calculation, 80% power, unilateral, due to difference in proportions, estimated loss of 25%.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology