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Clinical trials for Papanicolaou test

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
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    • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   44352   clinical trials with a EudraCT protocol, of which   7379   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    14 result(s) found for: Papanicolaou test. Displaying page 1 of 1.
    EudraCT Number: 2017-001205-33 Sponsor Protocol Number: V503-017 Start Date*: 2019-03-14
    Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
    Full Title: A Phase III Open-label Safety and Immunogenicity Study of GARDASIL™9 Administered to 9- to 26-Year-Old Females and Males in Vietnam
    Medical condition: Prevention of cervical, vulvar, vaginal, and anal cancers and related precancers, and anogenital warts caused by HPV Types 6, 11, 16, 18, 31, 33, 45, 52, and 58.
    Disease: Version SOC Term Classification Code Term Level
    20.1 100000004862 10063001 Human papilloma virus infection LLT
    Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
    Trial protocol: Outside EU/EEA
    Trial results: View results
    EudraCT Number: 2008-006208-52 Sponsor Protocol Number: IFN005 Start Date*: 2009-03-09
    Sponsor Name:Helix BioPharma Cooperation
    Full Title: Mono-centre, open-label study to investigate the multi-dose pharmacokinetics, efficacy and safety of Interferon alpha-2b Cream in women with a history of cytological diagnosed Pap IIID, with a con...
    Medical condition: cervical dysplasia (CIN I or CIN II; Pap IIID in the history, confirmed HPV+ status)
    Disease: Version SOC Term Classification Code Term Level
    9.1 10008263 Cervical dysplasia LLT
    Population Age: Adults Gender: Female
    Trial protocol: DE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-014552-30 Sponsor Protocol Number: UREP-01-2009 Start Date*: 2010-04-30
    Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de salut MAR)
    Full Title: Ensayo clínico exploratorio, prospectivo, aleatorizado, comparativo, para determinar la eficacia y seguridad de dos protocolos para hiperestimulación ovárica controlada en mujeres que van a ser tra...
    Medical condition: Mujeres diagnosticadas de esterilidad de origen desconocido
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2010-022151-32 Sponsor Protocol Number: FUNDEX001 Start Date*: 2011-02-03
    Sponsor Name:FUNDACION SANTIAGO DEXEUS FONT
    Full Title: Ensayo clínico fase II aleatorizado de cotratamiento con hormona de crecimiento recombinante humana dentro de un protocolo largo de estimulación ovárica bajo agonista de GnRH en mujeres con pobre r...
    Medical condition: Comprobar si la adición de rGH a un tratamiento estándar de estimulación ovárica controlada mejora la respuesta ovárica en mujeres con pobre respuesta previa. Los objetivos secundarios incluyen la...
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2010-019448-38 Sponsor Protocol Number: UREP-PREPENDO-2010 Start Date*: 2010-07-01
    Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar)
    Full Title: Ensayo clínico, prospectivo, aleatorizado, comparativo, para determinar la eficacia y seguridad de dos protocolos para preparación endometrial en mujeres subsidiarias de transferencia de embriones.
    Medical condition: Preparación endometrial en mujeres subsdiarias de tranferencia de embriones
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2016-004386-12 Sponsor Protocol Number: BHR-401-301 Start Date*: 2017-07-14
    Sponsor Name:Besins Healthcare Ireland Ltd.
    Full Title: Double-blind trial investigating the efficacy of different doses of Progesterone compared with Placebo for treatment of vasomotor symptoms
    Medical condition: Vasomotor symptoms
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004866 10020407 Hot flashes LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DE (Completed) AT (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2009-012457-37 Sponsor Protocol Number: 913-002 Start Date*: 2009-08-13
    Sponsor Name:Vantia Ltd
    Full Title: A Randomised, Double-Blind, Placebo-Controlled, Multicentre, Cross-Over Proof of Concept Study to Investigate the Efficacy and Safety of Pre-Emptive Administration of Repeated, Oral Doses of VA1119...
    Medical condition: Dysmenorrhoea
    Disease: Version SOC Term Classification Code Term Level
    12.0 10013935 Dysmenorrhoea LLT
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2006-001322-25 Sponsor Protocol Number: A4291023 Start Date*: 2006-07-20
    Sponsor Name:Pfizer, S.A.
    Full Title: A PHASE 2b MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, DOSE-RANGING STUDY EVALUATING THE EFFICACY AND SAFETY OF PD 0299685 FOR THE TREATMENT OF MODERATE TO SEVERE VASOMOTOR SYMPT...
    Medical condition: Treatment of moderate to severe vasomotor symptoms (hot flushes) associated with menopause
    Disease: Version SOC Term Classification Code Term Level
    8.1 10020408 Hot flushes LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2016-000158-36 Sponsor Protocol Number: OXYPEP202 Start Date*: 2016-03-18
    Sponsor Name:PEPTONIC medical AB
    Full Title: A Phase 2b, Double-blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the 12-week Efficacy of Vagitocin in Postmenopausal Women with Symptoms of Vulvovaginal Atrophy
    Medical condition: Vaginal Atrophy
    Disease: Version SOC Term Classification Code Term Level
    19.0 100000004872 10047782 Vulvovaginal atrophy LLT
    Population Age: Adults Gender: Female
    Trial protocol: SE (Completed)
    Trial results: View results
    EudraCT Number: 2016-002302-39 Sponsor Protocol Number: RSV-M-301 Start Date*: 2016-09-06
    Sponsor Name:Novavax, Inc.
    Full Title: A Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a Respiratory Syncytial Virus (RSV) F Nanoparticle Vaccine with Alumi...
    Medical condition: Respiratory syncytial virus (RSV) is the leading viral cause of severe lower respiratory tract disease in infants and young children worldwide. In industrialized countries, nearly all children have...
    Disease: Version SOC Term Classification Code Term Level
    20.0 10021881 - Infections and infestations 10061603 Respiratory syncytial virus infection PT
    Population Age: In utero, Newborns, Infants and toddlers, Under 18, Adults Gender: Male, Female
    Trial protocol: GB (Completed) ES (Completed) IT (Completed)
    Trial results: View results
    EudraCT Number: 2012-003227-38 Sponsor Protocol Number: EMR700623_535 Start Date*: 2013-03-07
    Sponsor Name:Merck Serono
    Full Title: A Multi-Centre, Two-Arm, Interventional, Phase IV Study to Evaluate Tailoring of Recombinant FSH Treatment in Subjects with Chronic Anovulation Using the Gonal-f® Prefilled Pen in Women Undergoing ...
    Medical condition: Anovulation in women with PCOS
    Disease: Version SOC Term Classification Code Term Level
    16.1 10042613 - Surgical and medical procedures 10033312 Ovulation induction PT
    16.1 100000004872 10065161 Polycystic ovarian syndrome LLT
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed) IE (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)
    Disease: Version SOC Term Classification Code Term Level
    20.1 10021881 - Infections and infestations 10004055 Bacterial vaginosis PT
    Population Age: Adults Gender: Female
    Trial protocol: PL (Completed) HU (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-015500-26 Sponsor Protocol Number: V503-006 Start Date*: 2010-03-24
    Sponsor Name:Merck & Co., Inc.
    Full Title: A Phase III Randomized, International, Placebo-Controlled, Double-Blind Clinical Trial to Study the Tolerability and Immunogenicity of V503, a Multivalent Human Papillomavirus (HPV) L1 Virus-Like P...
    Medical condition:
    Disease:
    Population Age: Adolescents, Under 18, Adults Gender: Female
    Trial protocol: SE (Completed) DK (Completed) Outside EU/EEA
    Trial results: View results
    EudraCT Number: 2004-000630-37 Sponsor Protocol Number: 308601 Start Date*: 2004-11-29
    Sponsor Name:Schering AG
    Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the safety, tolerability and efficacy of the CCR1 antagonist ZK 811752, given orally in a dose of 600 m...
    Medical condition: Endometrial pain
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: FI (Completed) SE (Completed) ES (Completed) CZ (Completed) DK (Completed)
    Trial results: View results
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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