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NCT03628092UNKNOWNanonymous

Laser Therapy for Vulvovaginal Symptoms in Breast Cancer Patients

Sponsor

Source record

Royal North Shore Hospital

Phase

Source record

Not Applicable

Modality

AI-normalized

medical device

Target

AI-normalized

Ablative carbon dioxide laser therapy targeting vulvovaginal atrophy (VVA) and genitourinary syndrome of menopause (GSM) symptoms.

Indication / condition

AI-normalized

Vulvovaginal Atrophy

Intervention

Source record

CO2 Fractional Ablative Laser, Placebo

Source & freshness

Source record

NCT ID

NCT03628092

Original source

ClinicalTrials.gov

Source last updated

Mar 12, 2020

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT03628092

Title

Laser Therapy for Vulvovaginal Symptoms in Breast Cancer Patients

Sponsor

Royal North Shore Hospital

Status

UNKNOWN

Phase

Not Applicable

Condition raw

Vulvovaginal Atrophy, Genitourinary Symptoms and Ill-Defined Conditions

Condition normalized

Vulvovaginal Atrophy, Genitourinary Symptoms and Ill-Defined Conditions

Modality raw

medical device

Modality normalized

medical device

Target raw

Ablative carbon dioxide laser therapy targeting vulvovaginal atrophy (VVA) and genitourinary syndrome of menopause (GSM) symptoms.

Target normalized

Ablative carbon dioxide laser therapy targeting vulvovaginal atrophy (VVA) and genitourinary syndrome of menopause (GSM) symptoms.

Interventions

CO2 Fractional Ablative Laser, Placebo

Public preview

Source record

The LAAVA2 trial, sponsored by Royal North Shore Hospital, explores the efficacy of fractional ablative CO2 laser therapy in alleviating vulvovaginal symptoms in breast cancer patients. This patient population is often underserved due to the side effects of cancer treatments, creating a niche market opportunity. If successful, this therapy could address a significant unmet need, potentially leading to a competitive advantage in the women's health segment. The trial's randomized, double-blind design enhances its credibility, which may facilitate future partnerships or licensing opportunities. The estimated enrollment of 70 participants suggests a focused study, but the overall status remains 'unknown,' indicating potential delays or challenges in recruitment.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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