Clinical TrialParallelEsketaminePlaceboCompleted

Clinical Study of Esketamine for Improving Depressive Symptoms in Patients With Lung Cancer After Smoking Cessation

Parallel-group controlled trial of intranasal esketamine (0.5 mg/kg) vs saline placebo in lung-cancer surgery patients with a long smoking history (≥20/day × 5+ years) undergoing smoking cessation. Target: 80 participants (40/40). Primary outcomes: HDRS-24, MADRS, CADSS, BPRS. Sponsor: Zhejiang Provincial People's Hospital, Hangzhou, China.

Target Enrollment
80 participants
Study Type
interventional
Design
Randomized, double Blind

Study Arms & Interventions

Esketamine

experimental

Intranasal delivery of esketamine (ESK) once a week for 8 sessions.

Interventions

  • Esketamine0.5 mg/kg
    via Intranasalweekly8 doses total

    Administered once a week for 8 sessions

Placebo

placebo

Intranasal delivery of normal saline placebo once a week for 8 sessions.

Interventions

  • Placebo
    via intranasalweekly8 doses total

    Normal saline placebo with a bittering agent added to simulate the taste of esketamine

Study Details

  • Status
    Completed
  • Type
    interventional
  • Design
    Randomizeddouble Blind
  • Target Enrollment80 participants
  • Timeline
    Start: 2023-02-24
  • Compounds

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