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286 studies found for:    fibroids
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Rank Status Study
21 Terminated
Has Results
Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in Premenopausal Women With Symptomatic Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Drug: Proellex;   Drug: Placebo
22 Terminated Fibroid Ablation Study - Large Fibroids
Conditions: Leiomyoma;   Uterine Fibroids;   Menorrhagia
Intervention: Device: VizAblate System
23 Completed
Has Results
Laparoscopic Radiofrequency Ablation (RFA) of Symptomatic Uterine Fibroids
Conditions: Uterine Fibroids;   Uterine Myomas
Intervention: Device: Halt Procedure
24 Completed
Has Results
Clinical Study of the Mirabilis High-Intensity Focused Ultrasound System for Non-Invasive Treatment of Uterine Fibroids
Condition: Uterine Fibroids (Leiomyomas)
Intervention: Device: Mirabilis High-Intensity Focused Ultrasound Treatment System
25 Completed MR Guided Focused Ultrasound Surgery in the Treatment of Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Device: ExAblate 2000
26 Active, not recruiting Biologic Predictors of Leiomyoma Treatment Outcomes
Conditions: Uterine Leiomyomas;   Fibroids;   Uterine Fibroids;   Myomas
Interventions: Genetic: DNA analysis;   Other: Hormonal analysis
27 Unknown  Laparoscopic Cryoablation of Uterine Fibroids
Condition: Symptomatic Uterine Fibroids
Intervention: Device: IceSense3 system
28 Completed Magnetic Resonance Guided Focused Ultrasound for Uterine Fibroids
Condition: Uterine Fibroids
Interventions: Procedure: MR Guided Focused Ultrasound;   Procedure: Placebo MR Guided Focused Ultrasound
29 Withdrawn Endometrial and Myometrial Changes, With and Without Fibroids
Condition: Fibroids
Intervention:
30 Withdrawn Safety and Efficacy of 25 and 50 mg Doses of Proellex® in Treating the Recurrence of Uterine Fibroid Symptoms
Condition: Uterine Fibroids
Intervention: Drug: Proellex
31 Recruiting Factors Influencing Volumetric MR-HIFU Ablation of Uterine Fibroids
Condition: Uterine Fibroid
Intervention: Device: Contrast-enhancement ultrasound with Sonovue
32 Completed
Has Results
A Prospective Study Comparing Contour SE™ Microspheres to Embosphere® Microspheres for Treating Symptomatic Uterine Fibroids With Uterine Fibroid Embolization (UFE)
Conditions: Leiomyoma;   Uterine Fibroids;   Uterine Neoplasms;   Menorrhagia;   Leiomyomatosis
Interventions: Procedure: Uterine Fibroid Embolization (UFE);   Device: Contour SE™ Microspheres;   Device: Embosphere® Microspheres
33 Not yet recruiting Targeted Vessel Ablation of Type 3 Uterine Fibroids With Magnetic Resonance Guided High Intensity Focused Ultrasound
Condition: Uterine Fibroid
Intervention: Device: Magnetic Resonance guided High Intensity Focused Ultrasound
34 Recruiting Safety and Tolerability of Collagenase Clostridium Histolyticum (EN3835) to Treat Uterine Leiomyoma (Fibroids)
Conditions: Fibroids, Uterine;   Leiomyoma
Interventions: Other: Saline;   Drug: EN3835
35 Unknown  Clinical Test of the MRgHIFU System on Uterine Fibroids
Condition: Uterine Fibroids
Intervention: Device: MRgHIFU system
36 Completed Efficacy Study of Magnetic Resonance (MR) Guided Focused Ultrasound in the Treatment of Large Fibroids
Condition: Uterine Fibroids
Intervention: Procedure: Magnetic Resonance Guided Focused Ultrasound
37 Recruiting Pilot of Letrozole for Uterine Myomas
Conditions: Leiomyoma;   Uterine Fibroids
Interventions: Drug: Letrozole;   Other: Placebo
38 Terminated South Miami Hospital Fibroid Registry
Condition: Uterine Myomas, Leiomyomas, or Fibromas.
Intervention:
39 Not yet recruiting Evaluation of Uterine Patency Following Sonography-guided Transcervical Ablation of Fibroids
Conditions: Uterine Fibroids;   Adhesions
Intervention: Device: Intrauterine ultrasound guided radio-frequency ablation
40 Not yet recruiting Treatment of Uterine Fibroids With Magnetic Resonance Guided High Intensity Focused Ultrasound
Condition: Uterine Leiomyoma
Interventions: Device: Magnetic Resonance Guided High Intensity Focused Ultrasound;   Drug: leuprolide acetate for depot suspension

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Study has passed its completion date and status has not been verified in more than two years.