A randomized controlled study of comparison of pain score after intramuscular injection of Benzathine penicillin in female patients with syphilis among cold compression before injection,1 % Lidocaine solution and combination between cold compression before injection and 1 % Lidocaine solutio

Phase 4

Recruiting

• Conditions: female patients with syphilis; Syphilis, Benzathine Penicillin, 1% Lidocain, cold compression, pain

• Registration Number: TCTR20200803003
• Lead Sponsor: Faculty of Medicine Siriraj Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-08-03
• Study Completion: 2021-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

1.female patients with syphilis
2.People who can inject BPG without contraindications
3.People who can communication with Thai

Exclusion Criteria

Drug allergy : BPG or Lidocaine

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain score at during intramuscular injection, 15 minutes after intramuscular injection and 30 minutes after int Visual analog scale

Secondary Outcome Measures

Name	Time	Method
pain score during injection at skin and during pull the needle from skin Visual analog scale,patient satisfaction after injection 30 minutes questionnaire