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Extended Observational Study Following Flexible-dose Treatment with Buagafuran Capsule in Generalized Anxiety Disorder

Extended Observational Study Following Flexible-dose Treatment with Buagafuran Capsule in Generalized Anxiety Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128677
Enrollment
Unknown
Registered
2026-07-23
Start date
2026-07-27
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Generalized Anxiety Disorder

Interventions

Positive-control group:NA
Placebo-control group:NA

Sponsors

Beijing An Ding Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Subjects who have signed the main trial informed consent form and have received at least one dose of the investigational product during or within the main trial period; 2. Be capable of fully understanding and signing the informed consent form for this extended observational study; 3. Subjects shall have no contraindications to venous blood collection, exhibit normal coagulation function, and be able to cooperate with the additional blood collection procedures scheduled at each visit.

Exclusion criteria

Exclusion criteria: 1. Subjects who have seriously violated the protocols of both the main trial and this observational study; 2. Subjects with severe anemia or coagulation disorders; 3. Other conditions judged by the investigator to render the subject ineligible for enrollment.

Design outcomes

Primary

MeasureTime frame
Cortisol levels;Plasma levels of Corticotropin-Releasing Factor;Omics-related indicators;Adrenocorticotropic Hormone;

Countries

China

Contacts

Public ContactGang Wang

Beijing An Ding Hospital, Capital Medical University

gangwangdoc@gmail.com+86 10 5930 3005

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026