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Study identifier: NCT06843044 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of Ranquilon in Patients With Anxiety Disorders Due to Neurasthenia and Adjustment Disorders

Condition: Anxiety · Neurasthenia · Adjustment Disorders  ·  Sponsor: Valenta Pharm JSC

PhasePhase 4
Planned participants250
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

Study is to evaluate the efficacy and safety of the drug Ranquilon, 1 mg tablets, at a dosage of 6 mg/day compared to the drug Afobazole, 10 mg tablets, at a dosage of 30 mg/day for the treatment of patients with anxiety disorders due to neurasthenia and adjustment disorders.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (6)

Engels Psychiatric Hospital State Health Care Institution of the Ministry of Health of the Saratov RegionEngel's, RussiaRecruiting
Unimed-C JscMoscow, RussiaRecruiting
Aurora MedFort LLCSaint Petersburg, RussiaRecruiting
Limited Liability Company "Research Center Eco-Safety"Saint Petersburg, RussiaRecruiting
Limited Liability Company "Stepmed Clinic"Saint Petersburg, RussiaRecruiting
Saratov City Psychoneurological DispensarySaratov, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06843044