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NCT06229353

Developing and Evaluating a Novel Approach to Improve HPV Vaccination Coverage Among High-risk, Under-immunized Adults Via the Emergency Department

Terminated Last updated 30 September 2025
What this trial tests

trial testing Gardasil 9 in Human Papilloma Virus in 34 participants. Terminated before completion.

Timeline
8 August 2024
Primary endpoint
30 July 2025
30 July 2025

Quick facts

Lead sponsorUniversity of Alabama at Birmingham
StatusTerminated
Study typeOBSERVATIONAL
Enrollment34
Start date8 August 2024
Primary completion30 July 2025
Estimated completion30 July 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Alabama at Birmingham

Who can join

Adults 18 to 45, any sex, with Human Papilloma Virus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To determine if the emergency department (ED) setting offers a viable space for improving HPV vaccination coverage among 18 to 45-year-old adults who have not yet received human papilloma virus (HPV) vaccination or who did not complete the vaccine series. This study will develop, pilot and evaluate an ED-based HPV vaccination protocol and program for ED patients aged 18-26 (for whom catch-up HPV vaccination is routinely recommended by the CDC) and separately for patients aged 27-45 (for whom it may be recommended under shared decision making, SDM).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Gardasil 9

Trials testing the same drug.

Other recruiting trials for Human Papilloma Virus

Currently open trials in the same condition.

Other University of Alabama at Birmingham trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06229353.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing