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RecruitingAccepts healthy volunteersPhase 3

LIMIT Trial - Lidocaine With Intramuscular Injection of Benzathine Penicillin G for Treponema Pallidum Treatment

Washington University School of Medicine · NCT06391125

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Phase 3
Target enrollment
48
US sites recruiting
1
Study start
July 1, 2024
Record last updated
March 25, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

There is evidence to suggest that lidocaine can help reduce the pain associated with intramuscular injections of benzathine penicillin G (BPG) or Bicillin, used to treat syphilis infections. A study published in the Journal of Family Practice in 2001 compared the pain experienced during bicillin injections with and without the use of lidocaine. The study found that patients who received lidocaine injections before receiving bicillin reported significantly less pain compared to those who received bicillin injections without lidocaine. Per the International Union against Sexually Transmitted Infections (IUSTI) European Guidelines for syphilis management, lidocaine has been used as a diluent for BPG since 1998. In the United States (US), BPG often comes prepackaged and lidocaine is unable to be used as a diluent with the same ease as it is in Europe. In light of this, the investigators propose a randomized controlled trial of benzathine penicillin G with and without lidocaine to quantify any site pain reduction with lidocaine in patients being treated for syphilis.

This study is a randomized, double blinded, placebo controlled trial. During this study, patients needing BPG treatment for syphilis will be screened for any penicillin allergies and consented to their participation. Each participant will receive 2 injections of BPG, 1.2 million units each (2x1.2 million units = 2.4 million units, the standard dose for syphilis treatment), as intramuscular injections, one in each gluteal muscle, with one of the injections randomly having 0.5ml of 1% lidocaine added while the other has 0.5 ml normal saline solution. The side of each injection will be randomized by the medical assistant (MA)/nurse filling the vials and the injecting MA will be blinded, as well as the study participant, as to which vial contains lidocaine and which contains normal saline. The participants will then be asked to rate their pain from 0-10 on each site of injection at 10 minutes post injection, then again at 24 hours after injection via email electronic survey (via RedCap). The differences in pain from the two injections will be compared and analyzed to see if lidocaine reduces pain associated with BPG injections compared to the control of normal saline added to BPG.

Being studied: normal Saline; Lidocaine

Conditions: Syphilis Infection; Benzathine Penicillin Adverse Reaction

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Adults 18 years of age or above
  • Confirmed syphilis diagnosis (reactive RPR with confirmatory treponemal testing)
  • Receiving first injection in series if patient requires 3x weekly injections for syphilis treatment

Exclusion Criteria

  • Penicillin allergy (anaphylaxis)
  • Lidocaine allergy (anaphylaxis)
  • Second or third injection in series if patient requires 3x weekly injections for syphilis treatment
  • Pregnancy

Recruiting US locations

  • WashU Infectious Diseases Clinic

    St Louis, MO 63110

    Site contact: Joseph N Cherabie, MD · 314-362-7827 · jcherabie@wustl.edu

Study contacts (from the official record)

  • Joseph Cherabie, MD · 7202858096 · jcherabie@wustl.edu
LIMIT Trial - Lidocaine With Intramuscular Injection of Benzathine… (NCT06391125) | Bored Studies