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A Study on the Safety and Effectiveness of Relafenopride a in Real-World Clinical Practice

A Study on the Safety and Effectiveness of Relafenopride a in Real-World Clinical Practice

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126519
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

locally advanced/recurrent or metastatic gastric cancer

Interventions

Based on the patient's tumor type, stage, and previous treatment history, participants will be enrolled into one of three different treatment regimen groups:None

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Signed informed consent and voluntarily participated. 2.Histologically or cytologically confirmed locally advanced, recurrent, or metastatic gastric cancer. 3.Aged >= 18 years. 4.Investigator-determined eligibility for relafenopride a therapy.

Exclusion criteria

Exclusion criteria: 1.Evidence of pregnancy or lactation in female patients. 2.Receiving treatment in a blinded trial. 3.Other ineligible conditions at the investigator’s discretion.

Design outcomes

Primary

MeasureTime frame
Safety analysis;real-world Progression-Free-Survival, rwPFS;

Secondary

MeasureTime frame
duration of therapy;adverse events;

Countries

China

Contacts

Public ContactLei Cong

Shandong Provincial Hospital

wdconglei@163.com+86 531 68777921

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026