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Lidocaine Before Esophageal Manometry and Ambulatory pH Monitoring

NCT03967197 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 304

Last updated 2023-01-19

No results posted yet for this study

Summary

A randomized controlled trial comparing esophageal manometry and ambulatory pH monitoring test tolerance in the presence versus in the absence of topical lidocaine.

Conditions

  • Pain, Acute

Interventions

DRUG

Saline spray

Physiologic saline spray

DRUG

Lidocaine Hydrochloride

Lidocaine hydrochloride 10% spray

Sponsors & Collaborators

  • Centre hospitalier de l'Université de Montréal (CHUM)

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-06
Primary Completion
2020-08-05
Completion
2020-08-05

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03967197 on ClinicalTrials.gov