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A clinical study to test how well the tablet ANXO-125 works in treating people with Generalized Anxiety Disorder (GAD).

A pilot study to evaluate the efficacy of tablet ANXO-125 in the management of generalized anxiety disorder (GAD). - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075951
Enrollment
30
Registered
2024-10-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Interventions

None listed

Sponsors

EVIMED SOLUTION
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed anxiety disorder. Willingness to comply with study requirements and follow instructions. Absence of significant cognitive impairment or comorbid psychiatric disorders. Ability to provide informed consent. Stable medication regimen for other medical conditions for at least 4 weeks prior to the

Exclusion criteria

Exclusion criteria: Individuals with known allergies to the contents of Drug. Pregnant or breastfeeding women. Individuals with associated comorbidities Recent participation in another clinical trial. Presence of severe medical conditions or unstable psychiatric disorders. Current substance abuse or dependence. Use of medications known to interact with the study drug Significant medical illness or unstable medical condition. Use of other anxiolytic medications within the past 4 weeks. Inability to comprehend or effectively communicate in the primary language of the study.

Design outcomes

Primary

MeasureTime frame
effectiveness of treatments in reducing symptoms mentioned in GAD scale.Timepoint: effectiveness of treatments in reducing symptoms mentioned in GAD scale in one month.

Secondary

MeasureTime frame
Monitoring for adverse effects such as Exacerbation of anxiety symptomsTimepoint: Monitoring for adverse effects such as Exacerbation of anxiety symptoms done during follow up 10th, 20th and 30th day of treatment

Countries

India

Contacts

Public ContactDr Yogini M Bhoyar

Dr D Y Patil College of Ayurveda and Research Centre

ashwin3485@gmail.com9405716548

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026