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62 studies found for:    Open Studies | "Leiomyoma"
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Open Studies | "Leiomyoma"
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Rank Status Study
1 Recruiting Vascular Function and Uterine Fibroids
Condition: Leiomyoma
Interventions: Device: Brachial artery catheter;   Drug: Acetylcholine;   Drug: Nitroprusside;   Drug: Norepinephrine;   Drug: Nitroprusside and phenylephrine
2 Recruiting Safety and Tolerability of Collagenase Clostridium Histolyticum (EN3835) to Treat Uterine Leiomyoma (Fibroids)
Conditions: Fibroids, Uterine;   Leiomyoma
Interventions: Other: Saline;   Drug: EN3835
3 Recruiting Ulipristal Acetate for the Preoperative Management of Hypoechoic Cellular Leiomyomas
Condition: Fibroid
Interventions: Drug: ulipristal acetate;   Drug: Leuprolide acetate
4 Recruiting Fertility After Poly-myomectomy Versus Uterine Artery Embolization for Symptomatic Uterine Fibroids
Condition: Multiple Leiomyoma
Interventions: Procedure: Poly-myomectomy;   Procedure: embolisation
5 Recruiting Ulipristal Acetate Versus GnRH Analogue Treatment Before Hysteroscopic Resection of Uterine Leiomyoma
Condition: Fibroid
Interventions: Drug: ulipristal acetate;   Drug: Leuprolide acetate
6 Recruiting A Multicenter Prospective Non-Interventional Study Assessing the Management of Canadian Women With Uterine Fibroids
Condition: Leiomyoma
Intervention: Other: No Intervention
7 Not yet recruiting Safety and Efficacy of Embozene Microspheres for Uterine Fibroid Embolization
Condition: Uterine Fibroids
Intervention: Procedure: Uterine Fibroid Embolization
8 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
9 Recruiting Factors Influencing Volumetric MR-HIFU Ablation of Uterine Fibroids
Condition: Uterine Fibroid
Intervention: Device: Contrast-enhancement ultrasound with Sonovue
10 Recruiting Satisfaction of Patients With Trans-Arterial Radial Access: Quality of Life in Uterine Fibroid Embolization Trial
Condition: Uterine Fibroid
Intervention: Procedure: Arterial access
11 Not yet recruiting Transcervical Radiofrequency Ablation of Uterine Fibroids Global Registry
Condition: Uterine Fibroid
Intervention: Device: Sonata System
12 Not yet recruiting Study of Volume Reduction of Uterine Fibroids After Embolization or Microwave Treatment
Condition: Uterine Fibroids
Interventions: Device: Microwave treatment, Emprint;   Procedure: uterine artery embolization
13 Recruiting Ulipristal Acetate Versus GnRH Analogue and Myometrial Preservation
Condition: Fibroid
Interventions: Drug: ulipristal acetate;   Drug: Leuprolide acetate
14 Recruiting Pregnancy Outcome Following Global Fibroid Ablation Using the Acessa™ System
Condition: One or More Uterine Fibroids
Intervention: Device: radiofrequency generator
15 Recruiting The Association Between Adenomyosis/Uterine Myoma and Lower Urinary Tract Symptoms
Conditions: Adenomyosis;   Uterine Leiomyoma
Intervention: Procedure: myomectomy or adenomyomectomy
16 Recruiting Misoprostol for Reduction of Blood Loss During Fibroid Surgery
Condition: Fibroids
Interventions: Drug: Misoprostol;   Drug: Placebo
17 Recruiting Effect of Hepatic Impairment on the Pharmacokinetics, Safety and Tolerability of BAY1002670 (Vilaprisan)
Condition: Leiomyoma
Intervention: Drug: Vilaprisan (BAY1002670)
18 Recruiting Power Morcellation Systems for Laparoscopic Hysterectomy and Myomectomy
Condition: Leiomyoma
Interventions: Device: EcoSac 230;   Device: EcoSac 400 ECO-T;   Device: GelPOINT Mini Advanced Access Platform
19 Recruiting Superior Hypogastric Nerve Block for Pain Control Post-UFE
Condition: Leiomyoma
Interventions: Procedure: Superior hypogastric nerve block;   Drug: 0.75% Ropivacaine;   Procedure: Subcutaneous injection;   Drug: 1% Xylocaine
20 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

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