- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Fallopian tubes.
Displaying page 1 of 2.
EudraCT Number: 2018-000230-35 | Sponsor Protocol Number: 014-FPO18 | Start Date*: 2018-10-17 | |||||||||||
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
Full Title: Phase II study on the combination of trabectedin and olaparib for advanced, platinum-resistant ovarian/tubes and primary of peritoneum cancer. - TROOPS trial (TRabectedin plus Olaparib in advanced ... | |||||||||||||
Medical condition: platinum-resistant ovarian carcinoma or Fallopian tubes or primary of peritoneum | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010095-23 | Sponsor Protocol Number: AA-GYN-002 | Start Date*: 2009-07-06 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Omrix Biopharmaceuticals Ltd | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A prospective, controlled, randomized, multi-center, pivotal study evaluating the safety and efficacy of ADHEXIL in prevention and/or reduction of adhesions in gynecology surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Adhesions in gynecology surgery. Surgeries involved will be ovarian cystectomy, endometriosis, inflammation, adhesiolysis Ovarian adhesion MedDRA 10067156 Tubal rupture MedDRA 10067553 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001271-16 | Sponsor Protocol Number: AGO-OVAR28 | Start Date*: 2022-08-01 | |||||||||||||||||||||
Sponsor Name:AGO Research GmbH | |||||||||||||||||||||||
Full Title: Niraparib vs Niraparib in combination with Bevacizumab in patients with carboplatinum-taxane based chemotherapy in advanced ovarian cancer (A multicentre randomised phase III trial) | |||||||||||||||||||||||
Medical condition: Patients with newly diagnosed, histologically confirmed, primary advanced invasive high grade epithelial ovarian cancer, peritoneal cancer, or fallopian tube cancer, FIGO stage III/IV (except FIGO ... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004752-21 | Sponsor Protocol Number: ISI-06-01 | Start Date*: 2006-11-08 | |||||||||||
Sponsor Name:Karolinska Institute, Danderyds hospital | |||||||||||||
Full Title: Pertubation with Lignocaine in Endometriosis Associated Symptoms Effect study (PLEASE) | |||||||||||||
Medical condition: Women 20-40 years of age with endometriosis and pelvic pain will be included in this study. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001950-16 | Sponsor Protocol Number: ISI-2015-1 | Start Date*: 2017-03-03 |
Sponsor Name:Isifer AB | ||
Full Title: A randomized, double blind, controlled, parallel group, multi-centre phase II clinical study of lidocaine pertubation as a treatment for couples with unexplained infertility | ||
Medical condition: Unexplained infertility | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-007013-20 | Sponsor Protocol Number: MK-0683-080 (P2135) | Start Date*: 2007-02-23 | |||||||||||
Sponsor Name:Onkologisk afdeling R and the Unit for Experimental Chemotherapy | |||||||||||||
Full Title: A Phase I/II non-comparative Study of Paclitaxel plus Carboplatin in combination with Vorinostat in patients with advanced, recurrent epithelial ovarian cancer | |||||||||||||
Medical condition: Advanced, recurrent epithelial ovarian cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004936-72 | Sponsor Protocol Number: WO42178 | Start Date*: 2021-08-25 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||||||||||||
Full Title: A PHASE II, OPEN-LABEL, MULTICENTER, PLATFORM STUDY EVALUATING THE EFFICACY AND SAFETY OF BIOMARKER-DRIVEN THERAPIES IN PATIENTS WITH PERSISTENT OR RECURRENT RARE EPITHELIAL OVARIAN TUMORS | ||||||||||||||||||||||||||||||||||||||
Medical condition: Persistent or Recurrent Rare Epithelial Ovarian Tumors | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) BE (Completed) IT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000365-33 | Sponsor Protocol Number: CHDR2043 | Start Date*: 2021-03-17 | |||||||||||
Sponsor Name:Molecular Partners AG | |||||||||||||
Full Title: A Phase 2a open label, non-comparative, single dose escalation study to evaluate the dynamics of viral clearance, pharmacokinetics and tolerability of ensovibep in patients with symptomatic COVID-1... | |||||||||||||
Medical condition: SARS-CoV-2 infection (COVID-19) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000189-31 | Sponsor Protocol Number: PRI04/2016 | Start Date*: 2017-05-12 |
Sponsor Name:Pannon Reprodukciós Intézet B.1.2 | ||
Full Title: Optimization and Safety Testing of Hormone Normalization Therapy in Advanced Maternal Age Infertile Women | ||
Medical condition: The therapy is intended to treat infertility that is caused by declining egg quality that occurs with advanced maternal age. The purpose of this pilot trial is to optimize the therapeutic protocol.... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000623-40 | Sponsor Protocol Number: BCD-100-5/FERMATA | Start Date*: 2019-12-02 | ||||||||||||||||
Sponsor Name:JSC BIOCAD | ||||||||||||||||||
Full Title: An International Randomized Double-blind Clinical Trial of BCD-100 Plus Platinum-based Chemotherapy with and without Bevacizumab versus Placebo Plus Platinum-based Chemotherapy with and without Bev... | ||||||||||||||||||
Medical condition: Advanced Cervical Cancer | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) AT (Prematurely Ended) DK (Completed) FI (Prematurely Ended) PL (Completed) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003413-35 | Sponsor Protocol Number: WN42349 | Start Date*: 2020-12-07 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A MULTICENTER, SINGLE ARM, OPEN-LABEL STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF SATRALIZUMAB IN PATIENTS WITH NEUROMYELITIS OPTICA SPECTRUM DISORDER (NMOSD) | |||||||||||||
Medical condition: Neuromyelitis Optic Spectrum Disorder | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) BG (Completed) PL (Completed) IT (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001326-26 | Sponsor Protocol Number: AA-GYN-001 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:Omrix Biopharmaceuticals Ltd. | |||||||||||||
Full Title: A Prospective, Controlled, Randomized, Multi-Center, Phase I/II Study Evaluating the Safety and Efficacy of Adhexil™ | |||||||||||||
Medical condition: Patients that undergo surgery that involves the ovaries | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002535-28 | Sponsor Protocol Number: 7343 | Start Date*: Information not available in EudraCT |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: Braking effect on myopia with atropine eye drops at 0.01%. | ||
Medical condition: Myopia | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003984-33 | Sponsor Protocol Number: 206OC201 | Start Date*: 2008-01-21 | ||||||||||||||||
Sponsor Name:Biogen Idec Limited | ||||||||||||||||||
Full Title: A Phase 2, Single-Arm Study of Volociximab Monotherapy in Subjects With Platinum-Resistant Advanced Epithelial Ovarian Cancer or Primary Peritoneal Cancer | ||||||||||||||||||
Medical condition: Platinum-Resistant Advanced Epithelial Ovarian Cancer or Primary Peritoneal Cancer | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-005110-22 | Sponsor Protocol Number: SNT-I-018 | Start Date*: 2017-11-20 |
Sponsor Name:Santhera Pharmaceuticals (Switzerland) Ltd | ||
Full Title: Phase-Ib/IIa study to investigate safety, tolerability, pharmacokinetics and pharmacodynamics of orally inhaled multiple doses of POL6014 in patients with Cystic Fibrosis | ||
Medical condition: Cystic fibrosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004644-24 | Sponsor Protocol Number: sorOVAR_07 | Start Date*: 2007-05-23 | |||||||||||
Sponsor Name:University of Bonn | |||||||||||||
Full Title: Prospective, open label, multi center phase II clinical trial with neoadjuvant chemotherapy in addition with Sorafenib in patients with primarily advanced ovarian cancer (FIGO IIIC + IV) and asci... | |||||||||||||
Medical condition: Ovarian Cancer; Stage FIGO IIIc and IV with more than 500 ml ascites | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002550-71 | Sponsor Protocol Number: SNT-I-018 | Start Date*: 2018-09-12 |
Sponsor Name:Santhera Pharmaceuticals (Switzerland) Ltd | ||
Full Title: Phase-Ib/IIa study to investigate safety, tolerability, pharmacokinetics and pharmacodynamics of orally inhaled multiple doses of POL6014 in patients with Cystic Fibrosis | ||
Medical condition: Cystic Fibrosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001938-11 | Sponsor Protocol Number: C22-109-08 | Start Date*: 2022-08-18 | |||||||||||
Sponsor Name:Pharma Holdings AS | |||||||||||||
Full Title: A Phase IIa, Randomised, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety and Tolerability of 3% LTX-109 compared to Placebo for nasal decolonisation of Staphylococcus aureus | |||||||||||||
Medical condition: Eradication of Staphylococcus aureus from the nose. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003023-14 | Sponsor Protocol Number: CSUC-02/21 | Start Date*: 2021-09-02 | |||||||||||
Sponsor Name:InDex Pharmaceuticals AB | |||||||||||||
Full Title: Pharmacokinetics of Cobitolimod Enemas in Participants with active Ulcerative Colitis | |||||||||||||
Medical condition: Moderate to Severe Active Ulcerative Colitis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006053-22 | Sponsor Protocol Number: NLX-112-DYS-101 | Start Date*: 2021-09-22 |
Sponsor Name:Neurolixis SAS | ||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability and Preliminary Efficacy of NLX-112 versus Placebo in Levodopa-induced Dyskinesia in Parkinson’s Disease | ||
Medical condition: Parkinson´s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
Query did not match any studies.