- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
85 result(s) found for: Endometriosis.
Displaying page 3 of 5.
EudraCT Number: 2021-001424-17 | Sponsor Protocol Number: CF113-302 | Start Date*: 2021-10-11 | |||||||||||
Sponsor Name:Chemo Research S. L. | |||||||||||||
Full Title: A multicentre, phase III, double-blind, randomised clinical trial to assess the efficacy and safety of LPRI-CF113 in the treatment of endometriosis versus placebo after 3 medication cycles followed... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) SK (Completed) CZ (Completed) LT (Completed) PL (Completed) HU (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002367-26 | Sponsor Protocol Number: CLI18001/Lita-003 | Start Date*: 2019-03-27 | |||||||||||
Sponsor Name:Litaphar Laboratorios | |||||||||||||
Full Title: A randomized, double-blind, three-arm, parallel-group, multicentre superiority study assessing the efficacy and safety of mifepristone (2.5 mg and 5 mg) vs. placebo for the treatment of endometrios... | |||||||||||||
Medical condition: endometriosis in reproductive-age | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001047-31 | Sponsor Protocol Number: M12-821 | Start Date*: 2014-05-14 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: Extension Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Subjects with Moderate to Severe Endometriosis-Associated Pain | |||||||||||||
Medical condition: Moderate to Severe Endometriosis Associated Pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) AT (Completed) IT (Completed) ES (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000283-26 | Sponsor Protocol Number: 18-OBE2109-003 | Start Date*: 2019-08-14 | |||||||||||
Sponsor Name:ObsEva S.A. | |||||||||||||
Full Title: A Phase 3 multicenter, randomized, double-blind, placebo-controlled, clinical study to assess the efficacy and safety of linzagolix in subjects with moderate to severe endometriosis-associated pain. | |||||||||||||
Medical condition: Endometriosis-associated pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) AT (Completed) CZ (Completed) PL (Completed) ES (Completed) BG (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000068-10 | Sponsor Protocol Number: 3142A2-203 | Start Date*: 2006-09-04 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | ||
Full Title: A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF 75 MG AND 150 MG DOSES OF ERB-041 ON THE REDUCTION OF SYMPTOMS ASSOCIATED WITH ENDOMETRIOSIS DURING TREAT... | ||
Medical condition: Reproductive-aged women with moderate to severe symptoms related to endometriosis. Subjects will have been diagnosed with endometriosis by laparoscopy or laparotomy within 10 years before visit 1B ... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-002791-14 | Sponsor Protocol Number: 1707-CL-0011 | Start Date*: 2013-02-14 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 2 Study to Assess the Efficacy, Safety, and Dose-Response Relationship of ASP1707 in Subjects with Endometriosis Associated Pelvic Pain for 12 ... | |||||||||||||
Medical condition: endometriosis associated pelvic pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000090-25 | Sponsor Protocol Number: TUC3PII-01 | Start Date*: 2021-06-23 | |||||||||||
Sponsor Name:TiumBio Co., Ltd. | |||||||||||||
Full Title: A Phase IIa, Multicenter, Randomized, Double-Blind, Parallel- Group, Placebo-Controlled, Proof of Concept Study to Evaluate the Efficacy and Safety of Orally Administered TU2670 in Subjects with Mo... | |||||||||||||
Medical condition: Moderate to Severe Endometriosis-Associated Pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002410-39 | Sponsor Protocol Number: 19-OBE2109-006 | Start Date*: 2020-04-14 | |||||||||||
Sponsor Name:ObsEva S.A. | |||||||||||||
Full Title: A double-blind randomized extension study to assess the long-term efficacy and safety of linzagolix in subjects with endometriosis-associated pain. | |||||||||||||
Medical condition: Endometriosis-associated pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) HU (Completed) BG (Completed) PL (Completed) AT (Completed) ES (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004378-92 | Sponsor Protocol Number: EdomTHC | Start Date*: 2019-05-27 | |||||||||||
Sponsor Name:Fundació Clínic per la Recerca Biomèdica | |||||||||||||
Full Title: Effect of cannabinoids (THC / CBD) on hyperalgesia in patients with deep endometriosis | |||||||||||||
Medical condition: Deep endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002783-40 | Sponsor Protocol Number: 000304 | Start Date*: 2019-07-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||||||||||||||||||||||
Full Title: A randomised, controlled, open label, parallel group, multicentre trial comparing the efficacy and safety of individualised FE 999049 (follitropin delta) dosing, using a long GnRH agonist protocol ... | |||||||||||||||||||||||||||||||||
Medical condition: Infertility in women undergoing assisted reproductive technologies (ART) such as an in vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) cycle | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) DK (Completed) NO (Completed) NL (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004353-80 | Sponsor Protocol Number: 179/2020 | Start Date*: 2021-01-04 |
Sponsor Name: | ||
Full Title: Laparoscopically inserted transversus abdominis plane block versus local wound anesthesia in laparoscopic peritoneal endometriosis surgery: a prospective randomized controlled double-blinded LTAP-t... | ||
Medical condition: The study subjects are patients with endometriosis needing surgical treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001789-13 | Sponsor Protocol Number: QUINA/2012 | Start Date*: 2012-11-16 |
Sponsor Name:Instituto de Investigacion Sanitaria La e | ||
Full Title: Double-blind, randomized, controlled contraceptives, parallel group, to assess the effect on nerve fibers in patients diagnosed with endometriosis grade III / IV symptomatic ascending-dose oral qui... | ||
Medical condition: Endometriosis grade III/IV | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004545-91 | Sponsor Protocol Number: 59874 | Start Date*: 2017-04-13 |
Sponsor Name:VU University Medical Center, department of reproductive Medicine | ||
Full Title: Continuous use of Oral contraceptives as an alternative for long term Pituitary down-regulation with GnRH agonist prior to IVF/ICSI in Endometriosis patients: a randomised controlled trial (COPIE t... | ||
Medical condition: The research population consists of women with surgically confirmed endometriosis ASRM stage III or IV or endometrioma on transvaginal ultrasound or MRI, scheduled for an IVF/ICSI treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001588-19 | Sponsor Protocol Number: MVT-601-3101 | Start Date*: 2017-11-01 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: SPIRIT 1: An International Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study to Evaluate Relugolix Administered with and without Low-Dose Estradiol and Norethindrone Ac... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) HU (Completed) BE (Completed) PL (Completed) BG (Completed) PT (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001098-26 | Sponsor Protocol Number: MK-7264-034 | Start Date*: 2018-09-21 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 2a, Proof of Concept, Randomized, Double-blind, Placebo-controlled Clinical Trial, to Evaluate the Efficacy and Safety of MK-7264 in Women with Moderate to Severe Endometriosis-related Pain | |||||||||||||
Medical condition: Moderate to severe Endometriosis-related pain (ERP) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004954-27 | Sponsor Protocol Number: | Start Date*: 2012-12-07 | |||||||||||
Sponsor Name:Clinical Trials and Research Governance, University of Oxford | |||||||||||||
Full Title: A single centre open-label randomised controlled trial of long term pituitary down-regulation before in vitro fertilisation for women with endometriosis: a pilot study | |||||||||||||
Medical condition: Sub-infertility due to endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003693-27 | Sponsor Protocol Number: CHDR1854 | Start Date*: 2019-02-06 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Intraoperative near-infrared fluorescence imaging of endometriosis with OTL38: a pilot study | ||
Medical condition: Endometriosis | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022216-39 | Sponsor Protocol Number: ENDOFIV | Start Date*: 2010-11-08 |
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
Full Title: ESTUDIO COMPARATIVO, RANDOMIZADO, CIEGO, DEL EFECTO DEL PRETRATAMIENTO CON ANÁLOGOS DE GNRH FRENTE A PLACEBO EN PACIENTES ESTÉRILES DIAGNOSTICADAS DE ENDOMETRIOSIS QUE REALIZAN TRATAMIENTO DE FECUN... | ||
Medical condition: La administración de un análogo de GnRH durante los tres meses previos a la realización de una FIV en pacientes con endometriosis/endometriomas puede mejorar la respuesta ovárica a la estimulación ... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004066-10 | Sponsor Protocol Number: MVT-601-3103 | Start Date*: 2018-10-19 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: SPIRIT EXTENSION: An International Phase 3 Open-Label, Single-Arm, Safety and Efficacy Extension Study to Evaluate Relugolix Co-Administered with Low-Dose Estradiol and Norethindrone Acetate in Wom... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) BE (Completed) FI (Completed) SE (Completed) PL (Completed) CZ (Completed) BG (Completed) PT (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001632-19 | Sponsor Protocol Number: MVT-601-3102 | Start Date*: 2017-12-01 | |||||||||||
Sponsor Name:Myovant Sciences GmbH | |||||||||||||
Full Title: SPIRIT 2: An International Phase 3 Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study to Evaluate Relugolix Administered with and without Low-Dose Estradiol and Norethindrone Ac... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) PL (Completed) GB (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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