The aim of the study is to answer the question, whether in patients with symptomatic and medically not sufficiently treatable uterine fibroids (population) the "Magnetic-Resonance-Guided Focused Ultrasound Surgery" short, MRgFUS-TUF (intervention) offers less burdensome therapy and patient-relevant advantages (symptom relief) compared to the operative myomectomy (comparison). The study will hence investigate the therapeutic benefit of this method.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
127
Magnetic Resonance Imaging-controlled high-focussed ultrasound
Myomectomy (laparoscopic or open surgical)
Krankenhaus Nordwest
Frankfurt am Main, Hesse, Germany
FOKUS Radiologische Gemeinschaftspraxis
Göttingen, Germany
Leipzig University
Leipzig, Germany
Marienhospital
Stuttgart, Germany
WAI question 4
Time to sustainably return to normal activities, based on the daily Work Activity Index (WAI) dimension, "Estimated Impairment of Disease Performance". The return to normal activities is considered to be given if the question "Hindrance of medical condition or injury at work?" (min max: 1: 'in my opinion, I am completely unable to work', 6: 'No Disability') is answered for at least three consecutive days with "No Disability" (6) or "I can do my job, but have complaints" (5).
Time frame: Until at least three consecutive days questionnaire was answered as indicated, up to 12 months
Symptom Severity Score of the UFS-QoL
The symptom severity is determined to be the co- primary endpoint for assessing therapeutic efficacy, based on the SSS (Symptom Severity Score) of the UFS-QoL (Uterine fibroid symptom and quality of life questionnaire). The co-primary assessment is performed 12 months after the primary treatment and for the evaluation the proportion of patients with at least 25 points improvement in the SSS is determined (0-100 scale, 100 indicating very strong symptoms, 0 no or low symptoms).
Time frame: 12 months after treatment
Hospital stay in days
Time frame: 12 months after treatment
Pain according to visual analog scale
Visual analog scale ranges from 0-100, 0 indicating no pain, 100 severe pain
Time frame: 12 months after treatment
Number of Adverse Events (AEs)
Time frame: 12 months after treatment
Number of postinterventional/postsurgery treatment complications
Time frame: 12 months after treatment
Number of re-interventions
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Time frame: 12 months after treatment
Alleviation of symptoms (irregular period, unfulfilled wish for child, pain, quality of life according to UFS-QoL
QoL: Quality of Life score regarding symptoms, ranges from 0-100, 0 indicating very low QoL, 100 indicating very high QoL
Time frame: 12 months after treatment
Health related quality of life according to UFS-QoL
QoL: Quality of Life score regarding health, ranges from 0-100, 0 indicating very low QoL, 100 indicating very high QoL
Time frame: 12 months after treatment
Sexuality related parameters according to UFS-QoL
QoL: Quality of Life score regarding sexuality, ranges from 0-100, 0 indicating very low QoL, 100 indicating very high QoL
Time frame: 12 months after treatment
Number of pregnancies and live births
Time frame: 12 months after treatment
Number of late complications like venous thromboembolisms within Follow up time frame
Time frame: 12 months after treatment
Number of fibroid recurrences (de novo fibroids) within Follow up time frame
Time frame: 12 months after treatment
Time period until return to normal physical activities, measured by the rate of patients, who achieved an a priori clinically relevant reduction of SSS of UFS-QoL
at timepoints: months 1, 3 and 6 compared to baseline.
Time frame: 12 months after treatment