- Trials with a EudraCT protocol (56)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
56 result(s) found for: Vulvar Diseases.
Displaying page 1 of 3.
| EudraCT Number: 2011-003134-13 | Sponsor Protocol Number: A551109 | Start Date*: 2012-02-13 | |||||||||||
| Sponsor Name:Erasmus MC | |||||||||||||
| Full Title: 5-Aminolevulinic Acid PhotoDynamic Therapy for the treatment of premalignant disorders of the vulva. | |||||||||||||
| Medical condition: Premalignant vulvar disorders (usual type Vulvar Intraepithelial Neoplasia) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000988-25 | Sponsor Protocol Number: version4 | Start Date*: 2012-04-27 |
| Sponsor Name:Gateshead Health NHS Trust Research & Development | ||
| Full Title: To determine the feasibility of using Microbubble technology to detect sentinel nodes in vulvar cancer. | ||
| Medical condition: Early stage vulvar cancer with no clinial or radiological evidence of lymph node metastases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002247-23 | Sponsor Protocol Number: MITOCERV4 | Start Date*: 2020-01-29 | ||||||||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
| Full Title: Single arm phase II study on Pembrolizumab in preneoplastic high grade HPV-related vulvar and cervical lesions | ||||||||||||||||||
| Medical condition: Patients with pre neoplastic high grade HPV-related vulvar and cervical lesions | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-002724-16 | Sponsor Protocol Number: CLS001-CO-PR-010;CHDR1508 | Start Date*: 2015-10-15 | |||||||||||
| Sponsor Name:Cutanea Life Sciences | |||||||||||||
| Full Title: A phase 2, randomized, double-blind, parallel-group study to assess the pharmacodynamics, safety/tolerability and efficacy of topical omiganan in patients with usual type vulvar intraepithelial neo... | |||||||||||||
| Medical condition: Patients with usual type vulvar intraepithelial neoplasia | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002052-17 | Sponsor Protocol Number: PITVIN | Start Date*: 2012-09-21 | |||||||||||
| Sponsor Name:Medizinische Universität Graz, Univ. Frauenklinik, Abteilung für Gynäkologie | |||||||||||||
| Full Title: Primary Imiquimod Treatment versus Surgery for Vulvar Intraepithelial Neoplasia: A Prospective Randomized Controlled Trial | |||||||||||||
| Medical condition: Vulvar intraepithelial neoplasia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2023-000128-12 | Sponsor Protocol Number: GinOnc-ECT | Start Date*: 2023-04-20 | ||||||||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | ||||||||||||||||||
| Full Title: Single-center phase II study on the use of electrochemotherapy in the treatment of Paget's disease and high-grade or initially invasive precancerous squamous lesions of the vulva (GinOnc-ECT study) | ||||||||||||||||||
| Medical condition: patients with newly diagnosed or recurrent high-grade or initially invasive precancerous squamous lesions of the vulva and non-invasive vulvar Paget's disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-003104-12 | Sponsor Protocol Number: M19VLC | Start Date*: 2020-01-14 | |||||||||||
| Sponsor Name:NKI-AVL | |||||||||||||
| Full Title: Treatment of locally advanced VULvar CArcinoma in a Neoadjuvant setting with Carboplatin and Paclitaxel chemotherapy | |||||||||||||
| Medical condition: vulvar carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000547-32 | Sponsor Protocol Number: 13123 | Start Date*: 2014-04-02 | |||||||||||
| Sponsor Name:University of Nottingham | |||||||||||||
| Full Title: A Randomised Controlled Trial of Adjunctive Systemic Therapy for Vulval Erosive Lichen Planus | |||||||||||||
| Medical condition: Vulval erosive lichen planus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004277-31 | Sponsor Protocol Number: E012-HPV | Start Date*: 2021-12-23 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:eTheRNA immunotherapies NV | ||||||||||||||||||||||||||||||||||||||
| Full Title: A phase I/IIa open label study to assess the safety, tolerability, immunogenicity and clinical activity of EI-201 mRNA immunotherapy given intravenously in subjects with recurrent or metastatic HPV... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Incurable recurrent or metastatic (R/M) HPV16-positive (HPV16+) tumors (e.g. oropharyngeal cancer, cervical, vulvar, vaginal, anal, penile cancer, etc.) | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) NL (Completed) PL (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-002201-25 | Sponsor Protocol Number: CHDR2007 | Start Date*: 2020-12-14 |
| Sponsor Name:Centre for Human Drug Research | ||
| Full Title: A two-part (observational and intervention) study to explore disease characteristics of vulvar (pre)malignancies compared to healthy volunteers | ||
| Medical condition: lichen sclerosus, vulvar (pre)malignancies | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006474-23 | Sponsor Protocol Number: BTIIMD-01-EC/21/LIQUEN | Start Date*: 2022-03-16 |
| Sponsor Name:BTI I MAS D S.L. | ||
| Full Title: Randomized, treatment-controlled clinical trial Conventional efficacy of Plasma Rich in Factors of Growth (PRGF®) in the treatment of atrophic vulvar lichen sclerosus | ||
| Medical condition: Vulvar Lichen Sclerosus et atrophicus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003952-63 | Sponsor Protocol Number: LIQUENIA | Start Date*: 2017-07-07 | |||||||||||
| Sponsor Name:Instituto de Investigación Sanitaria La Fe | |||||||||||||
| Full Title: Pilot study of vulval lichen sclerosus treatment by adipose tissue associated with autologous platelet-rich plasma | |||||||||||||
| Medical condition: Vulval lichen sclerosus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003973-16 | Sponsor Protocol Number: 2016-00601 | Start Date*: 2020-11-02 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Groningen International Study on Sentinel nodes in Vulvar cancer - III, a prospective phase 2 treatment trial | ||
| Medical condition: vulvar cancer patients with sentinel lymph node metastases larger than 2mm | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004864-37 | Sponsor Protocol Number: ASP-OP3-1 | Start Date*: 2018-05-16 | |||||||||||
| Sponsor Name:Aspen Global Incorporated | |||||||||||||
| Full Title: A Multinational, Phase 3, Double-blind, Placebo-Controlled, Randomized Study to Assess the Efficacy and Safety of Ovestin in the Treatment of Symptoms of Vulvar and Vaginal Atrophy in Postmenopausa... | |||||||||||||
| Medical condition: Vulvovaginal atrophy associated with menopause | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BG (Prematurely Ended) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000230-29 | Sponsor Protocol Number: CA209-358 | Start Date*: 2015-09-29 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab and Nivolumab plus Ipilimumab in Subjects with Virus-Positive and Virus-Negative Solid Tumors | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Virus-associated tumors | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Completed) DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-002614-13 | Sponsor Protocol Number: ElechtraPlatinum | Start Date*: 2022-03-07 | |||||||||||
| Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
| Full Title: Electrochemotherapy with Carboplatinum plus Bleomycin versus Bleomycin alone in vulvar cancer: the ElechtraPlatinum Study. A Randomized Controlled Trial | |||||||||||||
| Medical condition: relapsing vulvar carcinoma already subjected to multiple treatments | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000907-34 | Sponsor Protocol Number: H-200-001 | Start Date*: 2021-11-11 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Hookipa Biotech GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase I/II Study of TheraT® Vector(s) Expressing Human Papillomavirus 16 Positive (HPV 16+) Specific Antigens in Patients with HPV 16+ Confirmed Cancers | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) FR (Ongoing) NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-006059-13 | Sponsor Protocol Number: Tacho01 | Start Date*: 2012-04-16 | |||||||||||
| Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
| Full Title: The use of Tachosil as sealant in the prevention of lymphorrea after groin lymphadenectomy for vulvar cancer: a clinical controlled prospective trial | |||||||||||||
| Medical condition: lymphedema after groin lymphadenectomy in patients with vulvar cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000851-15 | Sponsor Protocol Number: M19CVT | Start Date*: 2020-01-16 | ||||||||||||||||
| Sponsor Name:NKI-AVL | ||||||||||||||||||
| Full Title: Treatment of metastatic vulvar carcinoma in a neoadjuvant setting with Carboplatin and Paclitaxel chemotherapy | ||||||||||||||||||
| Medical condition: vulvar carcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-002500-21 | Sponsor Protocol Number: Apollo01 | Start Date*: 2023-04-11 |
| Sponsor Name:LUMC | ||
| Full Title: Neo-adjuvant Pembrolizumab in vulvar squamous cell carcinoma: a clinical proof-of-concept study. | ||
| Medical condition: Vulvar squamous cell carcinoma (VSCC) Clinically diagnosed FIGO I-III primary VSCC patients to be treated with surgery with curative intent | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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