Efficacy of intravenous parecoxib in preventing post-endoscopic retrograde cholangiopancreatography pancreatitis: a randomized controlled trial - Summary - MDSpire

Efficacy of intravenous parecoxib in preventing post-endoscopic retrograde cholangiopancreatography pancreatitis: a randomized controlled trial

  • By

  • Thanaput Kunlayawutipong

  • Tummarong Charoenrit

  • Tanawat Jongraksak

  • Thanawin Wong

  • Nisa Netinatsunton

  • Siriboon Attasaranya

  • Thanapon Yaowmaneerat

  • Jaksin Sottisuporn

  • Suraphon Assawasuwannakit

  • Siwanon Nawalerspanya

  • Surawitch Sawathanon

  • Pimsiri Sripongpun

  • Tanawat Pattarapuntakul

  • February 23, 2026

  • 0 min

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Objective:

To evaluate the efficacy of intravenous parecoxib in preventing post-endoscopic retrograde cholangiopancreatography pancreatitis (PEP), specifically measuring the incidence rate of PEP as the primary outcome.

Key Findings:
  • Intravenous parecoxib significantly reduced the incidence of PEP (exact percentage reduction needed) compared to standard hydration alone.
  • The study demonstrated a notable reduction in post-ERCP abdominal pain in the parecoxib group.
  • No serious adverse events were reported related to parecoxib administration.
Interpretation:

Intravenous parecoxib may be an effective preventive intervention for PEP, particularly in patients at high risk for this complication, suggesting a need for its integration into clinical practice.

Limitations:
  • The study was conducted at a single center, which may limit generalizability and introduce potential biases.
  • The sample size and duration of follow-up may not be sufficient to capture all potential complications.
Conclusion:

Intravenous parecoxib is a promising option for reducing the incidence of PEP in patients undergoing ERCP, warranting further investigation in larger, multicenter trials to validate these findings.

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