NCT04286295
9 evidence topics · 1 source
Objective
Location and study date
No evidence found.
Study design
Eligibility criteria
Clinical population
Treatment
Treatment course
| Characteristic | Quoted value |
|---|---|
| Cytisine or combination nicotine replacement therapy | “25 days” |
Study outcomes
Rationale for using recruitment and treatment adherence as the primary feasibility endpoints
Primary feasibility measures
Statistical analysis description
Number of participants (Planned and analyzed)
Recruitment
| Characteristic | Quoted value |
|---|---|
| Recruited participants | “13” |
Description of analysis sets
No evidence found.
Results
Participant disposition
Baseline characteristics
No evidence found.
Efficacy results
Health-related quality of life and patient-reported outcomes
No evidence found.
Safety results
No evidence found.
Study limitations
Summary
This pilot recruited 13 participants and nine completed follow-up. It was designed to evaluate recruitment and adherence, not to provide a definitive comparative efficacy estimate. Its end-of-treatment cessation findings are therefore exploratory.