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Clinical trials
433 studies whose conditions map to this entity or one of its descendants. Status and phase are as posted on ClinicalTrials.gov. 50 studies per page.
| NCT | Title | Status | Phase | Enrollment (n) | Sponsor | Countries | Last update | Source |
|---|---|---|---|---|---|---|---|---|
| NCT00776074 | A Pharmacodynamic Study of Leuprorelin Gelatin-Free Formulation in Female Subjects With Uterine Fibroids. | completed | Phase 2 | 80 | TakedaINDUSTRY | 0 | Jun 22, 2010 | clinicaltrials |
| NCT00860002 | The Benefits and Limits of Laparoscopic Surgery for Uterine Fibroids | unknown | — | 1,200 | Taipei Veterans General Hospital, TaiwanOTHER_GOV | 1 | Jun 8, 2010 | clinicaltrials |
| NCT00444704 |
| Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of PRA-027 Administered to Healthy Japanese Females |
| completed |
| Phase 1 |
| — |
| Wyeth is now a wholly owned subsidiary of PfizerINDUSTRY |
| 1 |
| Jul 10, 2009 |
| clinicaltrials |
| NCT00910468 | Robot-Assisted Laparoscopic Myomectomy Is an Improvement Over Laparotomy in Patients With a Limited Number of Fibroids | completed | — | 150 | Ascher-Walsh, Charles, M.D.INDIV | 1 | May 29, 2009 | clinicaltrials |
| NCT00898170 | Effect of Myoma Removal on Blood Pressure and Erythropoetin Level | completed | N/A | 28 | Shiraz University of Medical SciencesOTHER | 1 | May 12, 2009 | clinicaltrials |
| NCT00584207 | Radiofrequency Ablation of Uterine Fibroids | terminated | Early Phase 1 | 15 | University of California, DavisOTHER | 1 | Apr 23, 2009 | clinicaltrials |
| NCT00712595 | Mifepristone for Treatment of Uterine Fibroids(Mifemyo) | completed | Phase 2 / Phase 3 | 200 | Mediterranea Medica S. L.OTHER | 1 | Apr 23, 2009 | clinicaltrials |
| NCT00826436 | Study Evaluating Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of PRA-027 in Japanese Postmenopausal Women | completed | — | 16 | Wyeth is now a wholly owned subsidiary of PfizerINDUSTRY | 1 | Mar 6, 2009 | clinicaltrials |
| NCT00156182 | A Long-Term Safety Study of Asoprisnil in the Treatment of Uterine Fibroids. | completed | Phase 2 | 38 | AbbottINDUSTRY | 0 | Mar 4, 2009 | clinicaltrials |
| NCT00354471 | Uterine Artery Embolization for Symptomatic Fibroids | completed | — | — | University of ManitobaOTHER | 1 | Feb 5, 2009 | clinicaltrials |
| NCT00821275 | Clinical Trial of Uterine Artery Embolization for Uterine Leiomyoma | unknown | Phase 2 / Phase 3 | 900 | Sun Yat-sen UniversityOTHER | 1 | Jan 13, 2009 | clinicaltrials |
| NCT00574418 | Far Infrared Radiation Treatment for Uterine Fibroids | unknown | Phase 1 | 2 | GAAD Medical Research Institute Inc.OTHER | 1 | Jan 5, 2009 | clinicaltrials |
| NCT00159328 | Efficacy Study of Magnetic Resonance (MR) Guided Focused Ultrasound in the Treatment of Large Fibroids | completed | Phase 4 | 50 | Imperial College LondonOTHER | 1 | Aug 13, 2008 | clinicaltrials |
| NCT00299481 | Tissue Bank of Biological Specimens From Patients With Gynecologic Disease | unknown | — | 7,000 | U.S. Army Medical Research and Development CommandFED | 1 | Jun 30, 2008 | clinicaltrials |
| NCT00390494 | Questionnaire Study to Assess Quality of Life After Treatment of Fibroids | unknown | — | 400 | U.S. Army Medical Research and Development CommandFED | 1 | Jun 30, 2008 | clinicaltrials |
| NCT00150644 | A Study to Evaluate the Effects of Asoprisnil(J867) in Women With Uterine Fibroids Who Are Scheduled for a Hysterectomy | completed | Phase 2 | 33 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00152256 | A Study to Evaluate of the Safety and Effectiveness of Asoprisnil in Treating Women With Uterine Fibroids | completed | Phase 3 | 239 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00152269 | Treatment of Uterine Fibroids With Asoprisnil(J867) | completed | Phase 3 | 475 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00156195 | Study to Evaluate the Safety of Asoprisnil in the Treatment of Uterine Fibroids | completed | Phase 3 | 523 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00156208 | Safety of Treatment of Uterine Fibroids With Asoprisnil | completed | Phase 3 | 166 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00160381 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment of Uterine Fibroids | completed | Phase 3 | 432 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00160459 | A Study to Evaluate the Safety and Effectiveness of Asoprisnil in the Treatment of Uterine Fibroids | completed | Phase 2 | 129 | AbbottINDUSTRY | 0 | May 29, 2008 | clinicaltrials |
| NCT00156156 | Study of Asoprisnil in the Treatment of Uterine Fibroids. | completed | Phase 3 | 149 | AbbottINDUSTRY | 0 | May 28, 2008 | clinicaltrials |
| NCT00001869 | Official Record of Patients Diagnosed With Lymphangioleiomyomatosis (LAM) | completed | — | 400 | National Heart, Lung, and Blood Institute (NHLBI)NIH | 1 | Mar 4, 2008 | clinicaltrials |
| NCT00087841 | Self-Hypnotic Relaxation Therapy During Invasive Procedures | completed | Phase 2 | 390 | National Center for Complementary and Integrative Health (NCCIH)NIH | 1 | Jan 17, 2008 | clinicaltrials |
| NCT00427544 | Study of the Safety, Tolerability, and PK of PRA-027 Administered to Women of Nonchildbearing Potential | completed | Phase 1 | — | Wyeth is now a wholly owned subsidiary of PfizerINDUSTRY | 1 | Dec 5, 2007 | clinicaltrials |
| NCT00351494 | Myoma Microvascularization Analysis Using Sonovue Before and After Uterine Artery Embolization | unknown | — | 40 | University Hospital, ToursOTHER | 1 | Nov 22, 2007 | clinicaltrials |
| NCT00562471 | Safety and Efficacy Study of a Hydrogel, Applied Following Removal of Myomas During Gynecologic Surgery, Administered for the Prevention/Reduction of Postoperative Adhesion Formation | completed | Phase 1 / Phase 2 | 76 | Angiotech PharmaceuticalsINDUSTRY | 3 | Nov 22, 2007 | clinicaltrials |
| NCT00067249 | Women's Use of Alternative Medicine: A Multiethnic Study | completed | — | 3,200 | National Center for Complementary and Integrative Health (NCCIH)NIH | 0 | Feb 27, 2007 | clinicaltrials |
| NCT00163930 | Post-Operative Pain Management in Patients Undergoing Uterine Artery Embolisation for Symptomatic Leiomyomata | unknown | — | — | Bayside HealthOTHER_GOV | 1 | Oct 3, 2006 | clinicaltrials |
| NCT00323999 | Hysteroscopic Monopolar and Bipolar Resection | unknown | N/A | — | Ullevaal University HospitalOTHER | 1 | May 10, 2006 | clinicaltrials |
| NCT00155870 | Health-Related QoL Among Women Receiving Hysterectomy in NTUH | unknown | — | 80 | National Taiwan University HospitalOTHER | 1 | Dec 20, 2005 | clinicaltrials |
| NCT00100191 | Emmy Trial: Uterine Artery Embolization (UAE) Versus Hysterectomy for Uterine Fibroids | completed | Phase 3 | 120 | ZonMw: The Netherlands Organisation for Health Research and DevelopmentOTHER | 1 | Jun 24, 2005 | clinicaltrials |
Data updated 22 days agoSource updated Jun 22, 2010source: clinicaltrials