- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Pelvic inflammatory disease.
Displaying page 1 of 2.
EudraCT Number: 2010-023254-36 | Sponsor Protocol Number: GUMPID002 | Start Date*: 2011-06-22 | |||||||||||
Sponsor Name:Brighton and Sussex University Hospitals NHS Trust | |||||||||||||
Full Title: Is a short course of azithromycin effective in the treatment of mild to moderate pelvic inflammatory disease (PID)? | |||||||||||||
Medical condition: Pelvic Inflammatory Disease (PID) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001602-24 | Sponsor Protocol Number: Th.B-1(2007):BTX(CP/CPPS) | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Department of Urology and Pediatric Urology - Justus-Liebig-University Giessen | |||||||||||||
Full Title: Intraprostatic injection of Botulinumtoxin type A in patients with chronic prostatitis / chronic pelvic pain syndrome (CP/CPPS) | |||||||||||||
Medical condition: chronic prostatitis / chronic pelvic pain syndrom | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011775-78 | Sponsor Protocol Number: 08GINE1 | Start Date*: 2009-01-20 |
Sponsor Name:UNIVERSITA` CAMPUS BIOMEDICO | ||
Full Title: Evaluation of efficacy of antibiotic prophylaxis in patients undergoing operative hysteroscopy | ||
Medical condition: Patients needing operative hysteroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004326-34 | Sponsor Protocol Number: MK8342B-060 | Start Date*: 2016-02-12 | ||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Placebo-Controlled Trial to Study the Efficacy and Safety of MK-8342B (ENG-E2 vaginal ring) in Women with Moderate to Severe Primary Dysmenorrhea. | ||||||||||||||||||
Medical condition: Moderate to severe primary dysmenorrhea | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | |||||||||||||||||
Trial protocol: SE (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001849-42 | Sponsor Protocol Number: BXL628 02 15 | Start Date*: 2005-07-13 | |||||||||||
Sponsor Name:BIOXELL SPA | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel group study to determine the effect of BXL628 in patients with Chronic Non-Bacterial Prostatitis category III Chronic Pelvic Pain Syndrome,... | |||||||||||||
Medical condition: Chronic Non-Bacterial Prostatitis category III Chronic Pelvic Pain Syndrome, CP/CPPS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005333-39 | Sponsor Protocol Number: WS982821 | Start Date*: 2012-01-17 |
Sponsor Name:National and Kapodistrial University of Athens | ||
Full Title: The effects of acute sildenafil administration on inflammatory markers in patients with vasculogenic erectile dysfunction. | ||
Medical condition: vasculogenic erectile dysfunction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-002152-26 | Sponsor Protocol Number: ISRCTN86894066 | Start Date*: 2009-01-20 | |||||||||||
Sponsor Name:The Royal Marsden Foundation Trust and The Institute of Cancer Research | |||||||||||||
Full Title: Randomised double-blind controlled phase III trial of hyperbaric oxygen therapy in patients suffering long-term adverse effects of radiotherapy for pelvic cancer | |||||||||||||
Medical condition: Chronic radiation-induced gastrointestinal symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017169-53 | Sponsor Protocol Number: BAY86-5258/13788 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:Bayer HelathCare AG | |||||||||||||
Full Title: Estudio multicéntrico, abierto, de un brazo de tratamiento para evaluar la seguridad y la eficacia de la administración oral diaria de 2 mg de Dienogest en el tratamiento de la endometriosis en ado... | |||||||||||||
Medical condition: Sospecha clínica o confirmada de endometriosis en mujeres adolescentes post-menarquia de 12 a menos de 18 años de edad (Clinically suspected or confirmed endometriosis in post menarche female adole... | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) FI (Completed) DE (Completed) AT (Completed) FR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004325-14 | Sponsor Protocol Number: MK8342B-059 | Start Date*: 2016-04-15 | ||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co.,Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial to Study the Efficacy and Safety of MK-8342B (ENG-E2 Vaginal Ring) in Women with Moderate to Severe Primary Dysmenorrhea (with Optional ... | ||||||||||||||||||
Medical condition: Treatment of primary dysmenorrhea | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002449-40 | Sponsor Protocol Number: P057-00 | Start Date*: 2012-10-12 |
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
Full Title: A multicenter, randomized, partially blinded, placebo-controlled clinical trial to evaluate the effect on primary dysmenorrheal of vaginal rings with an average daily release of 700 μg nomegestrol... | ||
Medical condition: This study will investigate the use of 4 doses of combined contraceptives (a progestin with an estrogen) in a vaginal ring dosage form for the treatment of dysmenorrhea (menstrual cramping pain). A... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DE (Completed) NO (Completed) NL (Completed) BE (Completed) SE (Completed) PL (Completed) DK (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004236-20 | Sponsor Protocol Number: MN4 | Start Date*: 2008-06-24 |
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | ||
Full Title: PET-CT DIAGNOSIS OF CARCINOMA PROSTATICO WITH ALTERNATIVE TO FLUORODESOSSIGLUCOSIO Radio: 18F-COLINA | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002135-30 | Sponsor Protocol Number: NCT04379973 | Start Date*: 2021-04-28 |
Sponsor Name:Antwerp University Hospital (UZA) | ||
Full Title: Live birth after additional tubal flushing with oil-based contrast versus no additional flushing: a randomised, multicentre, parallel group pragmatic trial in infertile women with at least one pate... | ||
Medical condition: Infertility defined as lack of conception despite 12 months of unprotected intercourse, or three cycles of donor insemination without pregnancy or three ovulatory ovulation induction cycles without... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004192-12 | Sponsor Protocol Number: NL66079.029.18 | Start Date*: 2019-08-05 |
Sponsor Name:Amsterdam UMC, location VU medical Center | ||
Full Title: Oil- based versus water-based contrast media for hysterosalpingography (HSG) in infertile women with unevaluated indications: a randomized controlled trial | ||
Medical condition: The research population consists of infertile couples who have tried to conceive for at least 12 months, or have oligo- or anovulation. We will focus on women with ovulation disorders, or at high r... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023083-40 | Sponsor Protocol Number: SPON830-10 | Start Date*: 2012-03-19 |
Sponsor Name:Cardiff University | ||
Full Title: A Phase II study of neoadjuvant chemotherapy given before SCPRT as treatment for patients with MRI-staged operable rectal cancer at high risk of metastatic relapse | ||
Medical condition: Rectal adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-004254-37 | Sponsor Protocol Number: 000400 | Start Date*: 2022-06-27 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled trial to assess the efficacy and safety of FE 999049 for treatment of men with idiopathic infertility | |||||||||||||
Medical condition: Idiopathic male infertility (including oligoasthenozoospermia) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Trial now transitioned) DE (Trial now transitioned) ES (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004226-15 | Sponsor Protocol Number: Can-Art1 | Start Date*: 2018-10-26 | ||||||||||||||||
Sponsor Name:King Christian 10th Hospital for Rheumatology | ||||||||||||||||||
Full Title: CAN-ART The efficacy and safety of using cannabis derivatives cannabidiol (CBD) and tetrahydrocannabinol (THC) for the treatment of pain in patients with inflammatory arthritis (RA, AS). A rand... | ||||||||||||||||||
Medical condition: Rheumatoid Arthritis (RA) and Ankylosing Spondylitis (AS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002255-10 | Sponsor Protocol Number: IRMINEpilot | Start Date*: 2016-06-30 | ||||||||||||||||||||||||||
Sponsor Name:Abertawe Bro Morgannwg University Health Board | ||||||||||||||||||||||||||||
Full Title: INFLAMMATORY RESPONSE IN MAJOR INJURY & RECOMBINANT HUMAN ERYTHROPOIETIN (IRMINE) - A PILOT STUDY | ||||||||||||||||||||||||||||
Medical condition: Post-trauma multiple organ failure: a manifestation of the systemic inflammatory/immune response to major injuries. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000164-10 | Sponsor Protocol Number: SPD476-112 | Start Date*: 2013-01-04 | |||||||||||
Sponsor Name:Shire Development LLC | |||||||||||||
Full Title: A Phase 1, Multicenter, Open-label Study to Determine the Safety and Pharmacokinetics of MMX Mesalamine Following Administration in Children and Adolescents With Ulcerative Colitis | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000541-24 | Sponsor Protocol Number: B1801381 | Start Date*: 2016-01-12 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A Multicenter Open-Label Study of Etanercept Withdrawal and Retreatment in Subjects with Non-Radiographic Axial Spondyloarthritis who Achieved Adequate 24 Week Response | |||||||||||||
Medical condition: Spondyloarthritis (SpA) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) BE (Completed) PL (Completed) HU (Completed) SE (Completed) ES (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005134-64 | Sponsor Protocol Number: AI424-020 | Start Date*: 2015-03-13 | |||||||||||
Sponsor Name:Bristol-Myers Squibb Company
[...]
1. Bristol-Myers Squibb Company
2. National Institute of Allergy and Infectious Diseases (NIAID) |
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Full Title: Phase I/II Open-Label, Pharmacokinetic and Safety Study of a Novel Protease Inhibitor (BMS-232632, ATAZANAVIR, ATV, REYATAZ™) in Combination Regimens in Antiretroviral Therapy (ART)-Naïve and Exper... | |||||||||||||
Medical condition: HIV Infections | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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