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Perioperative Oxaliplatin With S-1 Combined H. Pylori Eradication in the Management of Locally Advanced Gastric Cancer

StatusRecruiting
PhasePhase 2
Started
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Record History

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  1. Enrollment increased: 180 → 198 participantsv5
  2. Enrollment target: 198 to 180
    • Study description expanded, about 105 words
    v4
  3. Trial status: Not Yet Recruiting to Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Feb 28, 2026 to Dec 28, 2026
    • Start date changed from estimate of Aug 31, 2024 to Dec 31, 2024
    • Study sites: 0 to 1
    • Study completion date: Jul 31, 2028 to Jul 31, 2027
  4. Start date: Jul 31, 2024 to Aug 31, 2024v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study focuses on patients with H. pylori-positive resectable locally advanced adenocarcinoma of the gastric and oesophagogastric junction. It evaluates the perioperative oxaliplatin with S-1 (SOX) combined H. pylori eradication versus oxaliplatin with S-1 in the management of H. pylori-positive locally advanced adenocarcinoma of the gastric and oesophagogastric junction (cT3/4a Nx or T2 N2/3, M0) , assessing their values and advantages.
Trial Details
NCT Number NCT06510010
Lead Sponsor Sixth Affiliated Hospital, Sun Yat-sen University
Conditions
(from sponsor)		 Chemotherapy Effect
Enrollment 198 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov