- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
69 result(s) found for: Punch biopsy.
Displaying page 1 of 4.
EudraCT Number: 2015-004494-33 | Sponsor Protocol Number: 2015-004494-33 | Start Date*: 2016-01-20 | |||||||||||
Sponsor Name:Herlev and Gentofte Hospital | |||||||||||||
Full Title: Anti-IL-17, a possible new treatment for contact dermatitis? | |||||||||||||
Medical condition: allergic contact dermatitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002179-12 | Sponsor Protocol Number: PRILODE50-FUSION | Start Date*: 2022-09-16 | |||||||||||
Sponsor Name:Matilde Zaballos | |||||||||||||
Full Title: Determination of the effective dose 50 of intrathecal hyperbaric prilocaine required for the transrectal ultrasound guidance fusion-targeted prostate biopsy in ambulatory surgery | |||||||||||||
Medical condition: anaesthesia for prostate fusion biopsy in outpatient surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003740-39 | Sponsor Protocol Number: URO-CHUAC-BPSat-001. | Start Date*: 2016-04-12 | |||||||||||
Sponsor Name:Jose Luis Ponce Díaz-Reixa | |||||||||||||
Full Title: Open randomized clinical trial to examine individual pain tolerance in the use of two anesthetic techniques to perform saturation prostate biopsy . | |||||||||||||
Medical condition: Prostate biopsy anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018191-34 | Sponsor Protocol Number: FOL003 | Start Date*: 2010-07-21 | |||||||||||
Sponsor Name:Follica Inc. | |||||||||||||
Full Title: A Study to Explore the Effect of Controlled Cutaneous Perturbation and Pharmacologic Modulation for Inducing Follicular Neogenesis | |||||||||||||
Medical condition: Male subjects with androgenetic alopecia | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005592-12 | Sponsor Protocol Number: 76873 | Start Date*: 2021-08-30 | |||||||||||
Sponsor Name:Plastikkirurgisk og brystkirurgisk afdeling, Region Sjælland | |||||||||||||
Full Title: The effect of tranexamic acid on seroma formation after mastectomies | |||||||||||||
Medical condition: Immunomodulation of postoperative inflammatory reactions and thereby reduction of wound seroma by topical administration of tranexamic acid. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001381-38 | Sponsor Protocol Number: 1 | Start Date*: 2021-08-30 | |||||||||||
Sponsor Name:Plastikkirurgisk og brystkirurgisk afdeling, Region Sjælland | |||||||||||||
Full Title: Topical use of tranexamic acid for optimisation of wound healing in a novel, acute wound model | |||||||||||||
Medical condition: Immunomodulation of postoperative inflammatory reactions and thereby reduction of wound fluid production and improved healing by topical administration of tranexamic acid. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002545-38 | Sponsor Protocol Number: 68943 | Start Date*: 2019-09-13 | |||||||||||||||||||||
Sponsor Name:Bispebjerg Hospital, Department of Dermatology | |||||||||||||||||||||||
Full Title: Biodistribution of ablative fractional laser-assisted topical delivery of Vismodegib in basal cell carcinomas. | |||||||||||||||||||||||
Medical condition: Basal cell carcinoma Simple nodular basal cell carcinoma at any body locations | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002554-78 | Sponsor Protocol Number: PB-102-F02 | Start Date*: 2013-08-29 | |||||||||||
Sponsor Name:Protalix Ltd. | |||||||||||||
Full Title: An Extension of Phase 1/2, Open-Label, Dose Ranging Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Exploratory Efficacy Parameters of PRX-102 Administered by Intravenous Infusion ... | |||||||||||||
Medical condition: Fabry disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001458-10 | Sponsor Protocol Number: RN1002-0028 | Start Date*: 2004-12-21 | |||||||||||
Sponsor Name:Renovo Ltd | |||||||||||||
Full Title: A single site, placebo and standard-care controlled, double blind, randomised trial to investigate the efficacy of four doses of RN1002 in accelerating early wound healing of punch biopsy wounds | |||||||||||||
Medical condition: Wound Healing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000946-37 | Sponsor Protocol Number: R668-AD-1121 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, placebo-controlled study to assess the safety of REGN668 administered concomitantly with topical corticosteroids to patients with moderate-to-severe Atop... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005809-77 | Sponsor Protocol Number: NL38217 | Start Date*: 2013-01-31 |
Sponsor Name:Maastricht University Medical Centre | ||
Full Title: Treatment of superficial basal cell carcinoma by topical photodynamic therapy with fractionated 5-aminolevulinic acid 20% versus two stage topical photodynamic therapy with methylaminolevulinate | ||
Medical condition: Superficial basal cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000486-72 | Sponsor Protocol Number: ALA-AK-CT010 | Start Date*: 2017-07-28 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, double-blind, intra-individual, multi-center phase III study to evaluate the safety and efficacy of BF 200 ALA (Ameluz®) versus placebo in the treatment of mild to severe actinic kera... | |||||||||||||
Medical condition: Actinic keratosis (AK) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002678-11 | Sponsor Protocol Number: ICO-13-001 | Start Date*: 2018-06-07 |
Sponsor Name:Institut Català d’Oncologia | ||
Full Title: An open label biomarker pilot study of the antitumoral acrivity of denosumab in the pre-operative setting of early breast cancer | ||
Medical condition: early breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2020-000864-42 | Sponsor Protocol Number: IFX-1-P2.8 | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:InflaRx GmbH | |||||||||||||
Full Title: OPEN LABEL, MULTICENTER PHASE II STUDY OF THE C5A-ANTIBODY IFX-1 ALONE OR IFX-1 + PEMBROLIZUMAB IN PATIENTS WITH PD-1- OR PD-L1-RESISTANT/REFRACTORY LOCALLY ADVANCED OR METASTATIC CUTANEOUS SQUAMOU... | |||||||||||||
Medical condition: Locally advanced or metastatic cutaneous squamous cell carcinoma (cSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002856-26 | Sponsor Protocol Number: ADO-EP02(ML29328) | Start Date*: 2016-12-19 | |||||||||||
Sponsor Name:SRH Wald-Klinikum Gera GmbH | |||||||||||||
Full Title: A PHASE II, SINGLE-ARMED, MULTICENTER TRIAL OF NEOADJUVANT VISMODEGIB IN PATIENTS WITH LARGE AND/OR RECURRENT RESECTABLE BASAL CELL CARCINOMA | |||||||||||||
Medical condition: Patients with large and/or recurrent resectable basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002672-40 | Sponsor Protocol Number: SGNTUC-029 | Start Date*: 2022-09-20 | |||||||||||||||||||||
Sponsor Name:Seagen Inc. | |||||||||||||||||||||||
Full Title: An Open-label Randomized Phase 3 Study of Tucatinib in Combination with Trastuzumab and mFOLFOX6 versus mFOLFOX6 given with or without either Cetuximab or Bevacizumab as First-line Treatment for Su... | |||||||||||||||||||||||
Medical condition: unresectable or metastatic HER2+ colorectal cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NO (Trial now transitioned) SK (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) FR (Trial now transitioned) HU (Trial now transitioned) IE (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) AT (Trial now transitioned) GR (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002991-15 | Sponsor Protocol Number: SOLTI-1804 | Start Date*: 2019-11-04 |
Sponsor Name:SOLTI | ||
Full Title: HER2-PREDICT: Estudio Traslacional De Muestras De Tumor Procedentes De Los Ensayos Ds8201-A-U301 y Ds8201-A-U302 | ||
Medical condition: Her2‑positive, unresectable and/or metastatic breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002299-41 | Sponsor Protocol Number: KY1005-CT02 | Start Date*: 2019-01-24 | |||||||||||
Sponsor Name:Kymab Limited | |||||||||||||
Full Title: A Phase IIa, Randomised, Double Blind, Placebo Controlled, Parallel Group, Multicentre Study of an Anti OX40L Monoclonal Antibody (KY1005) in Moderate to Severe Atopic Dermatitis | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000197-30 | Sponsor Protocol Number: UoL001289 | Start Date*: 2018-07-13 |
Sponsor Name:The University of Liverpool | ||
Full Title: Sodium Valproate for Epigenetic Reprogramming in the Management of High Risk Oral Epithelial Dysplasia | ||
Medical condition: High Risk Oral Epithelial Dysplasia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004746-17 | Sponsor Protocol Number: 17HH4283 | Start Date*: 2018-03-05 |
Sponsor Name:Joint Research Compliance Office, Imperial College London and Imperial College Healthcare NHS Trust | ||
Full Title: Pain relief with disease modification by Capsaicin 8% patch: a clinical study in Diabetic Peripheral Neuropathy | ||
Medical condition: Diabetic painful neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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