Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06694714 · ClinicalTrials.gov registry record · Phase 4
Split Face Study of the Duration of Local Anesthetics - Fourth Arm
A Phase 4 study of Anesthesia, Local, sponsored by Weill Medical College of Cornell University.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 35
- Enrollment target
- 1
- Study location
NCT06694714: Recruiting Phase 4 study of Anesthesia, Local, sponsored by Weill Medical College of Cornell University.
NCT06694714 is a Phase 4 study of Anesthesia, Local that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 35 participants, below the 81-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06694714, a Phase 4 study of Anesthesia, Local, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 35 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a research study to compare how long injectable pain medications (anesthetics) commonly used in dermatologic surgery are effective for. The investigators will investigate the role of anesthetic volume on the duration of action at highly vascular sites.
Primary Outcome
To determine whether the time to return to baseline sensation differs significantly between each pair of anesthetics, the investigators will measure the time to return to baseline sensation at each anesthetized site by asking participants at 15 minute intervals if they can feel a sharp sensation at the site. Sterile needles will be used. The return of the sensitivity will be determined using binary outcomes (yes/no) and recorded on a standardized template. The maximum difference in anesthetic du
Conditions Studied
Interventions
- DRUG 0.5 ml lidocaine + epinephrine 1:100,000
- DRUG 1.0 ml lidocaine + epinephrine 1:100,000
Study Locations (1)
New York
- Weill Cornell Medicine - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2025-01-21 |
| Est. Completion | 2027-06-01 |
| Phase | Phase 4 |
What NCT06694714 shows while recruiting
NCT06694714 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 81-participant average among 18 other Anesthesia, Local trials with a reported enrollment target (57% lower).
The record links to 1 condition, with Anesthesia, Local appearing as the primary indexed condition, and to 2 interventions - of which 0.5 ml lidocaine + epinephrine 1:100,000 is the first listed.
NCT06694714 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06694714 about?
NCT06694714 is a clinical study titled "Split Face Study of the Duration of Local Anesthetics - Fourth Arm". This is a research study to compare how long injectable pain medications (anesthetics) commonly used in dermatologic surgery are effective for. The investigators will investigate the role of anesthetic volume on the duration of action at highly vascular sites.
What is the current status of trial NCT06694714?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 35 participants. The study started on 2025-01-21. Estimated completion is 2027-06-01.
What conditions does trial NCT06694714 study?
This clinical trial studies the following conditions: Anesthesia, Local.
What interventions are being tested in trial NCT06694714?
The interventions under investigation include: 0.5 ml lidocaine + epinephrine 1:100,000 (DRUG), 1.0 ml lidocaine + epinephrine 1:100,000 (DRUG).
Who is sponsoring clinical trial NCT06694714?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06694714 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Anesthesia, Local
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06694714's enrollment target sits among peer trials
35 15th of 18 higher than 4 of 18 other Anesthesia, Local trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Anesthesia, Local trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Erector Spinae Plane Block Catheters and Intrathecal Morphine for Hepatic Resection
RECRUITING · Phase 4
-
Intralipid® 20% for Reversal of Local Anesthetics
ACTIVE NOT RECRUITING · Phase 4
-
Clinical Trial Comparing Effectiveness of Buffered Versus Unbuffered Local Anesthetic in Children Ages 10-12 Years
COMPLETED · Phase 4
-
Trial of Injected Liposomal Bupivacaine vs Bupivacaine Infusion After Surgical Stabilization of Rib Fractures
COMPLETED · Phase 4
-
Study of OraVerse® for Safety and Efficacy in Pediatric Dental Patients
COMPLETED · Phase 4
-
Liposomal Bupivacaine Versus Bupivacaine for for Postoperative Pain Control in Shoulder Surgery
COMPLETED · Phase 4
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01697371 · 35 participants · NA
Proton Therapy in the Treatment of Liver Metastases
- NCT01940757 · 35 participants · Phase 1
Experimental Infection of Hookworm-naïve Adults With Dermally-applied Infectious Necator Americanus Hookworm Larvae
- NCT02235857 · 35 participants · NA
Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children
- NCT02637934 · 35 participants · Phase 1
Phase I Pilot Study of Biodistribution, Metabolism and Excretion of Novel Radiotracer [18F]Fluorthanatrace (FTT) by PET/CT
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI