Mirtazapine and olanzapine reduce anxiety and depression scores in oral cavity cancer patients.
This randomized controlled trial evaluated 144 patients with oral cavity cancer. The study aimed to assess the impact of pharmacological interventions on psychological distress, specifically anxiety and depression. No specific setting was reported. The population was defined by cancer type.
Participants received either mirtazapine 15 mg/day orally or olanzapine 5 mg/day orally. Treatment duration was assessed at the second and fourth weeks. No publication phase was reported. The setting was not reported.
Both groups demonstrated significant reductions in anxiety and depression scores over time with p<0.001. Anxiety scores decreased from 14.10 to 10.28 with mirtazapine and from 14.08 to 10.97 with olanzapine. Depression scores changed from 14.07 to 10.24 for mirtazapine and from 14.01 to 10.98 for olanzapine. No absolute numbers were reported.
Safety data regarding adverse events, serious adverse events, discontinuations, and tolerability were not reported. Limitations were not specified in the provided documentation. Practice relevance was also not reported. Funding sources were not reported. Conflicts of interest were not reported.
While statistical significance was observed, the lack of safety reporting requires caution. Clinicians must weigh the potential benefits against unknown risks when considering these agents for oral cavity cancer patients experiencing anxiety or depression. Careful monitoring is advised.