The Efficacy of High-Intensity Focused Ultrasound Therapy on Adenomyosis
ConditionAdenomyosis of Uterus
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorFar Eastern Memorial Hospital
About this trial
To assess the efficacy of High-Intensity Focused Ultrasound on adenomyosis
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The patient must be at least 18 years old.
Adenomyosis: There must be several dark areas on at least one side of the uterine wall; the uterine wall must be thickened; in addition, the thickened uterine wall must have a nonhomogeneous structure; and clinically, there must be dysmenorrhea or menorrhagia.
Disqualifiers
The patient currently has an acute lower urinary tract infection or intestinal inflammation.
The patient has previously undergone bladder or urethral surgery.
The patient has a history of urinary tract stones or tumors.
Trial population
Patients with symptomatic uterine adenomyosis:
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
High Intensity Focused Ultrasound
Procedure/SurgeryMRI guided High Intensity Focused Ultrasound
Treatment groups
20 Participants
are divided into 1 treatment groupGroup A: Adenomyosis1 intervention
Trial outcomes
Primary outcomes
1
Dysmenorrhea
The changes of VAS scores of dysmenorrhea
Time frame
6 monthsSecondary outcomes
1
Menorrhagia
The change of VAS scores of menorrhagia
Time frame
6 months2
Overactive bladder symptoms
The changes of Overactive Bladder Symptoms Scores
Time frame
6 months3
Female sexual function
The changes of female sexual function index scores
Time frame
6 months4
Bowel incontinence
The changes of the scores in the bowel incontience questtionnaires
Time frame
6 monthsSponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: