Anesthetic effect of topical lidocaine-prilocaine in thoracentesis and abdominocentesis

Phase 2

• Conditions: Condition 1: Pleural effusion. Condition 2: Fluid in peritoneal cavity.; Pleural effusion in conditions classified elsewhere; Ascites

• Registration Number: IRCT20191204045600N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

patient undergoing thoracentesis or abdominocentesis, ordered by attending physician
Alert
Patients giving their consent to intervention

Exclusion Criteria

being pregnant or breast-feeding
allergies to the amides
having any dermatologic conditions at the site of procedure
being G6PD
using systemic analgesic medications

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient pain perception by using 0-10 Numeric Rating Scale. Timepoint: immediately after the procedure. Method of measurement: 0-10 Numeric Rating Scale.;Patients’ satisfaction level. Timepoint: immediately after the procedure,after asking pain perception. Method of measurement: 1-4 scale.

Secondary Outcome Measures

Name	Time	Method
umber of attempts to perform paracentesis(either abdomonocentesis or thoracentesis). Timepoint: after the procedure. Method of measurement: Writing down the number of attempts.