# Evaluation of a Postcoital Sponge on Self-Reported Vaginal Health Parameters

> **NCT06530186** · NA · NOT_YET_RECRUITING · sponsor: **Atlantic Health System** · enrollment: 1000 (estimated)

## Conditions studied

- Vaginal Infection
- Vaginal Discharge
- Vaginosis
- Sexual Dysfunction

## Interventions

- **DEVICE:** LiviWell Postcoital Vaginal Insert

## Key facts

- **NCT ID:** NCT06530186
- **Lead sponsor:** Atlantic Health System
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2024-08-01
- **Primary completion:** 2024-12-31
- **Final completion:** 2025-01-31
- **Target enrollment:** 1000 (ESTIMATED)
- **Last updated:** 2024-07-31


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06530186

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06530186, "Evaluation of a Postcoital Sponge on Self-Reported Vaginal Health Parameters". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06530186. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
