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NCT06019533

A Trial on Contraceptive Efficacy, Safety and Tolerability of LVDS (Levonorgestrel Vaginal Delivery System) During 13 Cycles

Active, enrolled Phase 3 Last updated 21 February 2025
What this trial tests

Phase 3 trial testing LVDS in Contraception in 750 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
9 August 2023
Primary endpoint
30 April 2025
30 April 2026

Quick facts

Lead sponsorChemo Research
PhasePhase 3
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment750
Start date9 August 2023
Primary completion30 April 2025
Estimated completion30 April 2026
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Chemo Research

Who can join

Adults 15 to 45, female only, with Contraception. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Multicentre, single arm phase III trial to assess the pearl index of LVDS. The trial lasts 13 cycles.The assessments include (but are not limited to) recording demographic data, pregnancy tests, gynaecological examinations, laboratory tests and a quality of life questionnaire. Adolescents will undergo DXA scans to measure bone mineral density (at selected sites only). The women will be provided with an e-diary app for their smartphone, to record IP use and vaginal bleeding.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Contraception

Currently open trials in the same condition.

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/NCT06019533.

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