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OpenAny

Search clinical trial records

treg_post_call_valyu_health_trials_search

Find clinical study protocols and outcomes. Uses the caller's OpenAny gateway credentials. Charges and authorization are determined by the gateway.

Input Schema

NameRequiredDescriptionDefault
bodyYesFind clinical study protocols and outcomes. Usage limits: Restricted clinical-trial source, short responses, 1-10 results. Billed from total_deduction_dollars; trial records are not efficacy or safety certification. Draft retail price: at cost from the upstream USD meter; no markup. Only the documented data sources are allowed. Request contract: include all six declared body fields. Send search_type=proprietary, response_length=short, and the exact max_price and included_sources shown in the example; these are constrained source settings.

Schema Changelog

Changes observed during successful MCP inspections.

  1. First observed

TDQS

B3.4/5.0
Behavior3/5

Does the description disclose side effects, auth requirements, rate limits, or destructive behavior?

No annotations are provided, and the top description usefully discloses that the caller's OpenAny gateway credentials are used and that charges and authorization are gateway-determined. However, it does not itself explain result limits, source restrictions, or the disclaimer that trial records are not efficacy or safety certification; those details appear only in the nested body description.

Agents need to know what a tool does to the world before calling it. Descriptions should go beyond structured annotations to explain consequences.

Conciseness5/5

Is the description appropriately sized, front-loaded, and free of redundancy?

The description is two short sentences with no wasted wording, and the purpose is front-loaded. The credential/billing note is relevant and does not obscure the primary function.

Shorter descriptions cost fewer tokens and are easier for agents to parse. Every sentence should earn its place.

Completeness4/5

Given the tool's complexity, does the description cover enough for an agent to succeed on first attempt?

The tool has one nested body parameter with a rich schema description and no output schema. The top description covers purpose and gateway billing/authorization, while the body schema supplies the request contract, limits, and source constraints; only usage routing is notably thin.

Complex tools with many parameters or behaviors need more documentation. Simple tools need less. This dimension scales expectations accordingly.

Parameters3/5

Does the description clarify parameter syntax, constraints, interactions, or defaults beyond what the schema provides?

Schema description coverage is 100%, so the schema already documents the six required body fields and their constraints. The top-level description adds no parameter-specific meaning beyond what the schema provides, making the baseline 3 appropriate.

Input schemas describe structure but not intent. Descriptions should explain non-obvious parameter relationships and valid value ranges.

Purpose4/5

Does the description clearly state what the tool does and how it differs from similar tools?

The description uses a specific verb, 'Find,' and a clear resource, 'clinical study protocols and outcomes,' which matches the title's clinical trial records focus. It is distinguishable from generic web and economics search siblings, though it does not explicitly name an alternative.

Agents choose between tools based on descriptions. A clear purpose with a specific verb and resource helps agents select the right tool.

Usage Guidelines2/5

Does the description explain when to use this tool, when not to, or what alternatives exist?

There is no explicit when-to-use or when-not-to-use guidance. The description gives credential and billing behavior but does not route the agent between this tool and siblings such as health references search or broader search tools.

Agents often have multiple tools that could apply. Explicit usage guidance like "use X instead of Y when Z" prevents misuse.

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