ClinicalTrials.gov
public full text
Public Domain
Questioning Patients About Adverse Medical Events
This trial studies whether 3 different methods of asking patients about adverse medical events in a clinical trial affects the rate of reported side effects.
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Examining Patterns in the Involvement of Gastric Bypass Patients in Clinical Studies#873631
- Electronic Notification of Teratogenic Risks#1095480
- Event-Related Potential (ERP) Components in Clinical Diagnosis#966458
- Testing Response Bias on Sensitive Topics in Self- Versus Enumerator-administered Surveys#852359
- Clinical trial participant information leaflets overstate the harms/risks of participation and understate the benefits#159578
Record · ID 1183539
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive