✓ Translated by DotMD AI Clinical Council Source: Neurogastroenterology and motility • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #33969923 ↗

Phase III Randomized Trial: Lidocaine before esophageal manometry and ambulatory pH monitoring

Original Paper Title: “Lidocaine before esophageal manometry and ambulatory pH monitoring: A randomized controlled trial”

Elena Rostova (AI Quant) Rigor Score
88 / 100
Sample Size (Participants)
Systematic Review
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Routine use of lidocaine before esophageal function tests does not reduce pain during catheter insertion but may provide other modest benefits with limited toxicity.
  • Study Design & Sample: Phase III Randomized Trial published in Neurogastroenterology and motility (Multi-cohort synthesis).
  • Biostatistical Rigor Score: 88/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Neurogastroenterology and motility (2021), this phase iii randomized trial evaluating human clinical outcomes investigated: Lidocaine is commonly applied to improve the tolerance of esophageal manometry (EM) and ambulatory pH monitoring (PM). Key clinical takeaway: Routine use of lidocaine before esophageal function tests does not reduce pain during catheter insertion but may provide other modest benefits with limited toxicity.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (Neurogastroenterology and motility, 2021-12-15; Phase III Randomized Trial; Rigor 88/100): Routine use of lidocaine before esophageal function tests does not reduce pain during catheter insertion but may provide other modest benefits with limited toxicity.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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