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181 studies found for:    Leiomyoma: Clinical Trials

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Rank Status Study
1 Enrolling by invitation Clinical Trial of Uterine Artery Embolization for Uterine Leiomyoma
Condition: Leiomyoma
Intervention: Procedure: Interventional radiological or surgical management
2 Terminated Safety and Effectiveness Study of RF Ablation of Uterine Fibroids to Reduce Menstrual Bleeding: the Fibroid Ablation Study
Conditions: Leiomyoma;   Uterine Fibroids;   Menorrhagia
Intervention: Device: VizAblate Intrauterine Ultrasound-Guided RF Ablation
3 Completed
Has Results 		Pilot Study of MRI-Guided High Intensity Focused Ultrasound Ablation of Uterine Fibroids
Conditions: Uterine Fibroids;   Uterine Leiomyomata
Intervention: Device: Philips MR guided HIFU system
4 Recruiting Sonalleve Fibroid Ablation Pivotal Clinical Trial for MR-HIFU of Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Device: MR-HIFU treatment;   Device: Sham treatment
5 Recruiting China Clinical Trial for Therapeutic MR-HIFU Ablation of Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Device: MR-HIFU uterine fibroid treatment
6 Completed
Has Results 		Two Year Extension Study of the Selective Progesterone Receptor Modulator Proellex® (CDB-4124) in Pre-Menopausal Women With Symptomatic Leiomyomata Who Have Previously Completed Study ZPU 003
Condition: Uterine Fibroids
Interventions: Drug: Proellex®;   Drug: Placebo
7 Completed Fibroid Growth Study
Condition: Uterine Leiomyomas
Intervention:
8 Not yet recruiting Study of the Efficacy of Dienogest in the Treatment of Uterine Leiomyomas When Compared to Desogestrel and Goserelin
Condition: Uterine Leiomyoma
Interventions: Drug: Dienogest;   Drug: Goserelin;   Drug: Desogestrel
9 Completed Safety Study of ExAblate for the Treatment of Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Device: ExAblate
10 Withdrawn Efficacy and Safety Study of Ulipristal Acetate in Females With Anemia Associated With Uterine Leiomyoma
Condition: Leiomyomas
Interventions: Drug: Ulipristal Acetate;   Drug: Iron
11 Completed
Has Results 		Therapeutic Magnetic Resonance Imaging (MRI)-Guided High Intensity Focused Ultrasound (HIFU) Ablation of Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Device: Philips MRI-guided HIFU system
12 Completed Therapeutic MRI-HIFU Ablation of Uterine Fibroids in a 3T MRI Scanner
Condition: Uterine Leiomyomas
Intervention: Device: Philips MR-guided HIFU system
13 Recruiting Randomized Pilot Study for the Treatment of Cutaneous Leiomyomas With Botulinum Toxin
Conditions: Cutaneous Leiomyomas;   Hereditary Leiomyomatosis and Renal Cell Cancer
Interventions: Biological: Botulinum toxin type A;   Other: Placebo
14 Completed Risk Factors for Uterine Fibroids: A Case Control Study
Condition: Uterine Fibroids
Intervention:
15 Completed Study of Proellex in Pre-menopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex 12.5 mg;   Drug: Proellex 25 mg;   Drug: Placebo
16 Terminated A Study on the Efficacy of 10 mg Oral Mifepristone for the Treatment of Symptomatic Uterine Leiomyomas
Condition: Leiomyoma
Intervention: Drug: mifepristone
17 Completed A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids.
Condition: Leiomyoma
Intervention: Drug: Asoprisnil
18 Withdrawn To Evaluating the Safety and Efficacy of 25 and 50 mg Doses of Proellex® in Treating the Recurrence of Uterine Fibroid Symptoms in Premenopausal Women
Condition: Uterine Fibroids
Intervention: Drug: Proellex®
19 Completed Comparison Study in the Treatment of Uterine Fibroids Uterine Fibroid Embolization Using BeadBlock™ Embolic Agent
Conditions: Leiomyoma;   Leiomyomatosis;   Uterine Neoplasms
Interventions: Device: Uterine fibroid embolization BeadBlock™;   Device: Uterine fibroid embolization Embosphere®
20 Terminated Multicenter Study Evaluating the Safety of Proellex® in Premenopausal Women With Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex® 25 mg;   Drug: Proellex® 50 mg
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† Indicates status has not been verified in more than two years