Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05336825 · ClinicalTrials.gov registry record · NA

CO2 Laser vs Lidocaine for Vestibulodynia in Premenopausal Women

A NA study, sponsored by Atlantic Health System.

Completed
Registry status
NA
Development phase
10
Enrollment target

NCT05336825: Completed NA study, sponsored by Atlantic Health System.

NCT05336825 is a NA study that has completed, run by Atlantic Health System. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05336825, a NA study, has completed, sponsored by Atlantic Health System.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

CO2 laser energy is currently used widely for the treatment of postmenopausal women who have vaginal atrophy due to the lack of estrogen. However, its effect on premenopausal women with hormonally-mediated vulvar vestibulodynia is unknown. This study seeks to evaluate the effect of CO2 laser on young women and compare it to topical lidocaine.

Primary Outcome

visual analog pain scale to q-tip palpation

Interventions

  • DEVICE CO2 laser
  • DRUG Lidocaine patch 5%

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2019-04-01
Est. Completion 2021-01-31
Phase NA
Atlantic Health System

43 total trials

What the finished NCT05336825 record still lists

NCT05336825 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which CO2 laser is the first listed.

NCT05336825 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05336825 about?

NCT05336825 is a clinical study titled "CO2 Laser vs Lidocaine for Vestibulodynia in Premenopausal Women". CO2 laser energy is currently used widely for the treatment of postmenopausal women who have vaginal atrophy due to the lack of estrogen. However, its effect on premenopausal women with hormonally-mediated vulvar vestibulodynia is unknown. This study seeks to evaluate the effect of CO2 laser on youn...

What is the current status of trial NCT05336825?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2019-04-01. Estimated completion is 2021-01-31.

What interventions are being tested in trial NCT05336825?

The interventions under investigation include: CO2 laser (DEVICE), Lidocaine patch 5% (DRUG).

Who is sponsoring clinical trial NCT05336825?

This trial is sponsored by Atlantic Health System, which has 43 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05336825's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

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

Source: ClinicalTrials.gov NCT05336825, the US trial registry maintained by the National Library of Medicine. NCT05336825 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.