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A Study Comparing Tofisopam and Clonazepam in Reducing Anxiety Symptoms in Adults with Generalized Anxiety Disorder

A comparison of the anxiolytic properties of Tofisopam and Clonazepam A randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092417
Enrollment
60
Registered
2025-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F411- Generalized anxiety disorder Health Condition 2: F410- Panic disorder [episodic paroxysmal anxiety] Health Condition 3: F401- Social phobias Health Condition 4: F400- Agoraphobia

Interventions

Intervention1: Tofisopam: It will be started along with escitalopram at a dose of 50 mg once daily. Based on the response and clinical improvement, it may be increased to a maximum dose of 200 mg per

Sponsors

Kurma Ramya Krishna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who are diagnosed with any anxiety disorder according to the International Classification of Diseases (ICD-11). This includes the diagnosis of phobias, panic disorders, and generalized anxiety disorder. 2. Past diagnosis of mental illness, but not on medication for at least 3 months.

Exclusion criteria

Exclusion criteria: 1. Organic causes for the anxiety symptoms. 2. Presence of uncontrolled medical conditions such as hypertension, diabetes mellitus, bronchial asthma, etc. 3. Presence of severe medical conditions that might interfere with assessment, such as cancer, renal problems, cardiac problems, etc. 4. Pregnancy 5. Unwilling to participate in the study.

Design outcomes

Primary

MeasureTime frame
Changes in scores of the Hamilton Anxiety Rating ScaleTimepoint: Changes in scores of the Hamilton Anxiety Rating Scale at baseline, 2 weeks, and 4 weeks.

Secondary

MeasureTime frame
To compare the tolerability between the two anxiolytics by a generic assessment of the Side Effects scale.Timepoint: Baseline, 2 weeks, and 4 weeks.

Countries

India

Contacts

Public ContactKurma Ramya Krishna

Konaseema Institute of Medical Sciences and Reseach foundation

ramyakrishna251@gmail.com08332885221

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026