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Transcervical Radiofrequency Ablation of Uterine Fibroids Global Registry (SAGE): Study Protocol and Preliminary Results

Authors Christoffel L, Römer T, Schiermeier S

Received 9 January 2021

Accepted for publication 11 February 2021

Published 3 March 2021 Volume 2021:14 Pages 77—84

DOI https://doi.org/10.2147/MDER.S301166

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Scott Fraser


Ladina Christoffel, 1 Thomas Römer, 2 Sven Schiermeier 3

1Spital Oberengadin, Samedan, Switzerland; 2Evangelisches Klinikum Köln-Weyertal, Köln, Germany; 3Marien-Hospital, Witten, Germany

Correspondence: Ladina Christoffel
Spital Oberengadin, Via Nouva 3, Samedan, CH-7503, Switzerland
Tel +41 81851 8111
Email [email protected]

Background: Transcervical fibroid ablation (TFA) is a minimally invasive, effective treatment of symptomatic uterine fibroids that utilizes intrauterine ultrasound for imaging and radiofrequency energy for ablation. Outcomes reported with TFA have been positive, with significant reductions in fibroid volume, improvements in symptom severity and health-related quality of life, and low complication and surgical reintervention rates. The SAGE registry characterizes the long-term (5-year) outcomes of TFA when used to treat symptomatic uterine fibroids in real-world usage.
Methods/Design: SAGE is an ongoing postmarket global registry involving up to 50 sites and up to 500 women who select TFA with the Sonata system for treatment of symptomatic uterine fibroids. Patients are followed for 5 years. Main outcomes include symptom severity score and health-related quality of life subscales of the UFS-QoL, general health status on the EQ-5D, perceived treatment benefit, treatment satisfaction, work and activity patterns, overall patient treatment outcome, adverse events, pregnancy incidence and outcomes, and surgical reinterventions for heavy menstrual bleeding.
Discussion: The SAGE registry represents the largest known study of TFA for uterine fibroids and will generate up to 2500 patient-years of outcome data. Preliminary results from the first 160 treated women suggest broad applicability of TFA to a wide range of fibroid types and sizes and an excellent safety profile, with a device-related adverse event rate of 0.6% and a serious procedure-related adverse event rate of 0.6%. Of the 241 fibroids treated, 10% were submucous, 52% transmural, 28% intramural, and 10% subserous. Ablated fibroid diameters ranged from < 1 cm to > 10 cm, with 27% of fibroids having maximum diameters > 5 cm. The real-world experience from SAGE will strengthen the existing evidence on the durability of TFA in providing meaningful relief from uterine fibroid symptoms and will have important clinical and economic implications for patients, physicians, and healthcare payers.
Trial Registration: https://clinicaltrials.gov, NCT03118037. Registered on 18 April 2017.

Keywords: leiomyoma, myoma, radiofrequency ablation, SAGE, Sonata, transcervical fibroid ablation, uterine fibroid

Corrigendum for this paper has been published

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