ClinicalTrials.gov record
Completed Early Phase 1 Interventional Accepts healthy volunteers

Immediate Post-Operative Anesthesia With Either Lidocaine or Bupivacaine

ClinicalTrials.gov ID: NCT06293807

Public ClinicalTrials.gov record NCT06293807. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 14, 2026, 7:22 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Immediate Post-Operative Anesthesia With Either Lidocaine or Bupivacaine: A Short-term Clinical Response

Study identification

NCT ID
NCT06293807
Recruitment status
Completed
Study type
Interventional
Phase
Early Phase 1
Lead sponsor
The University of Texas Health Science Center at San Antonio
Other
Enrollment
72 participants

Conditions and interventions

Interventions

  • Bupivicaine 0.5% with 1:200,000 epinephrine Drug
  • Placebo Other
  • Xylocaine 2 % with 1:100,000 epinephrine Drug

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 5, 2022
Primary completion
Apr 15, 2023
Completion
Apr 15, 2023
Last update posted
Mar 7, 2024

2022 – 2023

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
The University of Texas Health Science Center at San Antonio San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06293807, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 7, 2024 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06293807 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →