- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Myomectomy.
Displaying page 1 of 1.
EudraCT Number: 2010-019810-26 | Sponsor Protocol Number: 1968 | Start Date*: 2011-09-09 | |||||||||||
Sponsor Name:King's College Hospital Foundtion NHS Trust | |||||||||||||
Full Title: A randomised controlled trial to investigate the effects of the use of pre-operative GnRH analogue and intra-operative mechanical tourniquet for myomectomy on surgical blood loss, future fertility ... | |||||||||||||
Medical condition: Uterine Fiboids | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002832-15 | Sponsor Protocol Number: 49916 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:VU university medical center | |||||||||||||
Full Title: Ulipristal versus Gonadotropin-releasing hormone agonists prior to laparoscopic myomectomy: a double blind randomized controlled trial | |||||||||||||
Medical condition: Uterine fibroids are very common during reproductive years in women. Minimally invasive treatments are emerging. Myomectomy is the gold standard which removes the fibroids entirely, preferably lapa... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005120-16 | Sponsor Protocol Number: 62638 | Start Date*: 2018-11-02 | |||||||||||
Sponsor Name:Amsterdam UMC, Location VUmc | |||||||||||||
Full Title: Ulipristal versus standard surgical treatment in symptomatic uterine fibroids | |||||||||||||
Medical condition: Uterine fibroids are very common during reproductive years in women. Minimally invasive treatments are emerging. Myomectomy is the gold standard, preferably laparoscpically, because it removes the ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004098-17 | Sponsor Protocol Number: 35195 | Start Date*: 2009-03-31 |
Sponsor Name:East Tallinn Central Hospital | ||
Full Title: Double-Blind, Randomized, Placebo -Controlled Study to Evaluate the Efficacy of Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in th... | ||
Medical condition: Pre-operative Administration of Etoricoxib 120 mg, Etoricoxib 120 mg and Paracetamol 1 g Combination or Placebo in the Treatment of Postoperative Pain in Patients Undergoing Gynaecologic Laparoscop... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: EE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002333-21 | Sponsor Protocol Number: 1 | Start Date*: 2006-07-28 |
Sponsor Name:Allgemeines Krankenhaus Wien, Medizinische Un iversität Wien [...] | ||
Full Title: Intraoperative Goal-Directed Fluid Therapy in Lean and Obese Patients | ||
Medical condition: Hemodynamics in obese patients differ from lean patients: Obese patients have a higher cardiac output, the absolute amount of their intravascular volume is increased, as is the intracellular volume... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000964-16 | Sponsor Protocol Number: 1311-BCN-138-DG | Start Date*: 2015-03-30 |
Sponsor Name:IVI Valencia | ||
Full Title: Uterine fibroids: Impact of ulipristal acetate 10 mg on ART results. | ||
Medical condition: Uterine Fibroids and Assisted Reproduction | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001719-39 | Sponsor Protocol Number: INN-CB-002 | Start Date*: 2008-07-23 | |||||||||||
Sponsor Name:Innocoll Technologies | |||||||||||||
Full Title: A Phase II, Single Dose, Blinded, Prospective Study to Investigate the Efficacy and Safety of the CollaRx® Bupivacaine Implant in Women following Abdominal Hysterectomy or other Nonlaparoscopic Ben... | |||||||||||||
Medical condition: To investigate the efficacy and safety of the CollaRx Bupivacaine Implant in women following abdominal hysterectomy or other nonlaparoscopic benign gynecological procedure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004602-86 | Sponsor Protocol Number: | Start Date*: 2005-11-21 |
Sponsor Name:Medical University of Vienna | ||
Full Title: A comparison of crystalloids vs. colloids for intraoperative goal-directed fluid management | ||
Medical condition: Fluid optimization has been considered as major contributor to improved oxygen delivery, and thus improved outcome in patients. Hypovolemia has been associated with significant increases in morbid... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001804-22 | Sponsor Protocol Number: PGL07-021 | Start Date*: 2008-10-16 | |||||||||||
Sponsor Name:PregLem S.A. | |||||||||||||
Full Title: A Phase III, randomized, parallel group, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of PGL4001 (ulipristal) versus placebo for pre-operative treatment of... | |||||||||||||
Medical condition: Uterine myoma are benign, monoclonal, hormone sensitive, smooth muscle tumors of the uterus. It is the most common tumor of the female reproductive tract in pre-menopausal women and mostly asympto... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001805-40 | Sponsor Protocol Number: PGL07-022 | Start Date*: 2008-07-28 | |||||||||||
Sponsor Name:PregLem S.A. | |||||||||||||
Full Title: A Phase III, randomised, parallel group, double-blind, double-dummy, active comparator -controlled, multi-center study to assess the efficacy and safety of PGL4001 (ulipristal) versus GnRH-agonist ... | |||||||||||||
Medical condition: Uterine myomas are benign, monoclonal, hormone sensitive, smooth muscle tumors of the uterus. It is the most common tumor of the female reproductive tract in pre-menopausal women and mostly asympt... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) AT (Completed) FR (Completed) IT (Completed) PL (Completed) DE (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018999-25 | Sponsor Protocol Number: PGL09-026 | Start Date*: 2010-07-13 | |||||||||||
Sponsor Name:PregLem S.A. | |||||||||||||
Full Title: Estudio multicéntrico de fase III para investigar la eficacia y la seguridad del tratamiento abierto de 3 meses con PGL4001, seguido de un periodo aleatorizado, doble ciego y controlado con placebo... | |||||||||||||
Medical condition: Los miomas uterinos son tumores benignos, monoclonales y sensibles a las hormonas, del músculo liso del útero. Son los miomas que aparecen con más frecuencia en el aparato reproductor femenino en l... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) AT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
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