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NCT03028610

Pregnancy Outcome Following Global Fibroid Ablation Using the Acessa™ System

Completed NA Last updated 9 December 2024
What this trial tests

NA trial testing radiofrequency generator in One or More Uterine Fibroids in 23 participants. Completed in 13 August 2023.

Timeline
1 January 2016
Primary endpoint
13 July 2023
13 August 2023

Quick facts

Lead sponsorUniversity Hospital Tuebingen
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment23
Start date1 January 2016
Primary completion13 July 2023
Estimated completion13 August 2023
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital Tuebingen

Who can join

Adults 18 to 40, female only, with One or More Uterine Fibroids. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Prospective, interventional, single-center, longitudinal, single-arm pilot study to evaluate pregnancies following the Acessa™ treatment of uterine myomas in women who desire future childbearing

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other University Hospital Tuebingen 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/NCT03028610.

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