- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Bacterial vaginosis.
Displaying page 1 of 2.
EudraCT Number: 2011-002386-38 | Sponsor Protocol Number: CLVS100VER | Start Date*: 2011-09-30 | |||||||||||
Sponsor Name:VERISFIELD (UK) LTD | |||||||||||||
Full Title: | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011826-32 | Sponsor Protocol Number: RFX-VAG/002/2008 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Alfa Wassermann S.p.A. | |||||||||||||
Full Title: A phase II, multicentre, double-blind, randomised, placebo-controlled study on efficacy and tolerability of Rifaximin vaginal tablets in the treatment of bacterial vaginosis | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007874-39 | Sponsor Protocol Number: PGX401-08 | Start Date*: 2009-03-19 | ||||||||||||||||||||||||||
Sponsor Name:Innotech international | ||||||||||||||||||||||||||||
Full Title: Etude multicentrique en ouvert sur l'efficacité et la tolérance d'un traitement local avec polygynax au cours des vaginites mycosiques et/ou bactériennes | ||||||||||||||||||||||||||||
Medical condition: Vaginites Mycosiques et/ou bactériennes | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002489-15 | Sponsor Protocol Number: 380119 | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:Medinova AG | |||||||||||||
Full Title: Comparative study of the efficacy and safety of vaginally applied Dequalinium Chloride (10 mg) and orally applied Metronidazole (2 x 500 mg) in the treatment of bacterial vaginosis | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004563-37 | Sponsor Protocol Number: IPR_GARDEFLORA_15-2 | Start Date*: 2016-12-27 | |||||||||||
Sponsor Name:Laboratoires IPRAD PHARMA | |||||||||||||
Full Title: Study of the efficacy and safety of treatment with completely lyophilised cultures of Lactobacillus crispatus - IP 174178 administered intravaginally in the treatment of bacterial vaginosis. | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003356-51 | Sponsor Protocol Number: ZEL001 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Zelmic AB | |||||||||||||
Full Title: A single-centre, open-label, single-arm, Phase I/II study to investigate the effect of a hydrogen peroxide foam on clinical signs and symptoms and the vaginal flora in patients with bacterial vagin... | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000694-39 | Sponsor Protocol Number: SPL7013-018 | Start Date*: 2014-10-22 | |||||||||||
Sponsor Name:Starpharma Pty Ltd | |||||||||||||
Full Title: A phase 3, double-blind, multicentre, randomised, placebo-controlled study to determine the efficacy and safety of SPL7013 Gel (VivaGel®) to prevent the recurrence of bacterial vaginosis | |||||||||||||
Medical condition: recurrent bacterial vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004398-89 | Sponsor Protocol Number: 380104 | Start Date*: 2006-12-06 | |||||||||||
Sponsor Name:Medinova AG | |||||||||||||
Full Title: Comparative Study of the Efficacy of 10 mg Dequalinium Chloride (Fluomizin®) in the Local Treatment of Bacterial Vaginosis | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004483-19 | Sponsor Protocol Number: RRK5908 | Start Date*: 2017-09-09 | |||||||||||
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial to assess the clinical and cost effectiveness of topical lactic acid gel for treating second and subsequent episodes of bacterial vaginosis | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004579-16 | Sponsor Protocol Number: FU-04-21 | Start Date*: 2022-01-18 | |||||||||||
Sponsor Name:Adamed Pharma S.A. | |||||||||||||
Full Title: A Phase II, Randomized, Parallel design, Open label, Dose ranging Study to evaluate the efficacy and safety of Furazidin vaginal tablets in women with bacterial vaginosis | |||||||||||||
Medical condition: Bacterial Vaginosis (BV) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004292-41 | Sponsor Protocol Number: BECRO/VF/FEMALE | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Verisfield (UK) Ltd., Greek branch | |||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a Generic Formulation of Vaginal Ovule conta... | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001759-22 | Sponsor Protocol Number: PGX401-11 | Start Date*: 2015-07-24 | |||||||||||||||||||||||||||||||
Sponsor Name:Laboratoire Innotech International | |||||||||||||||||||||||||||||||||
Full Title: Assessment of the efficacy of POLYGYNAX® in the empirical treatment of infectious vaginitis International, multicentre, randomised, double-blind, parallel group study, comparative versus miconazole | |||||||||||||||||||||||||||||||||
Medical condition: Patients presenting with abnormal vaginal discharge associated with other vaginal symptoms (i.e. vaginal burning and/or vaginal irritation and/or vaginal pain) clinically evoking infectious vaginit... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) CZ (Completed) SK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-017901-12 | Sponsor Protocol Number: LYO_2009-09 | Start Date*: 2010-02-26 | |||||||||||
Sponsor Name:LYOCENTRE | |||||||||||||
Full Title: Etude de l’efficacité et de la tolérance du traitement par la culture totale lyophilisée de lactobacillus casei variété rhamnosus (Lcr35 Lc) administré par voie vaginale dans la prévention de réci... | |||||||||||||
Medical condition: vaginose bactérienne récidivante | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007659-15 | Sponsor Protocol Number: NC-07-03 | Start Date*: 2008-04-22 | ||||||||||||||||||||||||||
Sponsor Name:Lumavita AG | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase II Study to Investigate the Efficacy, Safety, and Tolerability of 3 doses of SPK 0602 (pentamycin) Vaginal Tablets vs Placebo (veh... | ||||||||||||||||||||||||||||
Medical condition: Symptomatic Vaginitis due to Bacterial Vaginosis, Candidiasis or Trichomoniasis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: EE (Completed) DE (Completed) HU (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002918-12 | Sponsor Protocol Number: 1-2013-HU | Start Date*: Information not available in EudraCT |
Sponsor Name:Amvac Kft | ||
Full Title: Randomized, prospective, double blind clinical study to evaluate the effectiveness, dosage and safety of lactobacillus vaccine for management of bacterial vaginosis in a non-selected patient popula... | ||
Medical condition: Bacterial vaginosis (Nugent score 4 or above) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004890-10 | Sponsor Protocol Number: KI DS 200509 | Start Date*: 2006-02-17 |
Sponsor Name:Kvinnokliniken | ||
Full Title: Vaginal colonization of the LN bacteria (patented human lactic acid producing bacteria) when conventional treatment of bacterial vaginosis and Candida vaginitis is followed by treatment with Vagipi... | ||
Medical condition: Diagnosed Bacterial Vaginosis (BV) or Candida Vaginitis(CV) ICD: N76.8 (BV); N77.1*B37.3+(CV) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000752-33 | Sponsor Protocol Number: SPL7013-016 | Start Date*: 2012-06-22 |
Sponsor Name:Starpharma Pty Ltd | ||
Full Title: A phase 3, double-blind, multicenter, randomized, placebo-controlled study to assess the efficacy and safety of SPL7013 Gel (VivaGel®) for the treatment of bacterial vaginosis | ||
Medical condition: Bacterial vaginosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002819-25 | Sponsor Protocol Number: GU18/108645 | Start Date*: 2020-04-22 | |||||||||||
Sponsor Name:Leeds Teaching Hospital NHS Trust | |||||||||||||
Full Title: Dequalinium versus usual care antibiotics for the treatment of bacterial vaginosis (DEVA): a multicentre, randomised, open label, non-inferiority trial | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002376-41 | Sponsor Protocol Number: MICINT | Start Date*: 2018-09-10 | |||||||||||
Sponsor Name:Zealand University Hospital, Gynecological department | |||||||||||||
Full Title: Modulating the Vaginal Microbiome after Implantation Failure - A randomized placebo controlled study of lactobacilli supplements | |||||||||||||
Medical condition: Sub-optimal vaginal and/or endometrial microbiome. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003147-22 | Sponsor Protocol Number: GLBR-101-2011 | Start Date*: 2011-12-02 | |||||||||||
Sponsor Name:Glenmark Farmaceutica LTDA | |||||||||||||
Full Title: A Multicenter, Open-Label, Comparator-Controlled, Parallel Group, Phase 3 Study to Assess the Efficacy and Safety of Clotrimazole/Clindamycin (200 mg/100 mg FDC) Ovules Compared with Metronidazole ... | |||||||||||||
Medical condition: vaginitis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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