- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
26 result(s) found for: Cosmetic Surgery.
Displaying page 1 of 2.
EudraCT Number: 2005-004262-16 | Sponsor Protocol Number: PDTMohs05 | Start Date*: 2006-01-20 | |||||||||||
Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A trial comparing Metvix® photodynamic therapy (PDT) followed by Mohs micrographic surgery with Mohs micrographic surgery alone for the treatment of basal cell carcinoma (BCC) | |||||||||||||
Medical condition: Basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000063-10 | Sponsor Protocol Number: RD.03.SPR.29040 | Start Date*: 2004-10-07 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: A comparison of Metvix PDT with simple excision surgery in subjects with superficial Basal cell Carcinoma (sBCC) | |||||||||||||
Medical condition: Superficial Basal Cell Carcinomas, occurring mostly on trunk and extremities (4,5), are progressively spreading, slow growing cancers. They can be difficult to diagnose and often mistaken for oth... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009986-32 | Sponsor Protocol Number: OZR-2008-12 | Start Date*: 2009-06-30 |
Sponsor Name:Rotterdam Eye Hospital | ||
Full Title: Continuation of platelet inhibiting drugs in eyelid surgery. A randomized, double-masked, placebo-controlled clinical trial. | ||
Medical condition: Patients, using platelet inhibiting drugs, due for eyelid surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002459-40 | Sponsor Protocol Number: BREAST-AB-01 | Start Date*: 2020-12-17 |
Sponsor Name:Rigshospitalet | ||
Full Title: Prophylactic treatment of breast implants with a solution of gentamicin, vancomycin and cefazolin antibiotics for women undergoing breast reconstructive surgery: a randomized controlled trial (The ... | ||
Medical condition: Implant-based breast reconstruction following mastectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001659-11 | Sponsor Protocol Number: BELKYRA-HYPOGASTRIUM | Start Date*: 2018-10-19 |
Sponsor Name:COSMETIC SURGERY BCN SLP | ||
Full Title: A pilot study to evaluate the safety and efficacy of the application of Belkyra™ in the fat located in the hypogastric zone. | ||
Medical condition: Subjects with fat located in the treatment area (hypogastrium) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002635-28 | Sponsor Protocol Number: 69081 | Start Date*: 2019-10-14 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: The effect of hyperbaric oxygen therapy on breast cancer patients with late radiation toxicity | ||
Medical condition: Late radiation toxicity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021270-11 | Sponsor Protocol Number: CL2-05682-102 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Impact of Daflon 500 mg on the progression of chronic venous disease and symptoms in patients operated on for varicose veins with conservation of the great saphenous vein. A multicentre, double bl... | |||||||||||||
Medical condition: Patients suffering from chronic venous disease and for whom ASVAL (Ambulatory Selective Varicose veins Ablation Local anesthesia) surgery is indicated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005124-42 | Sponsor Protocol Number: KEKLUKACS-CLIN-02 | Start Date*: 2014-03-17 |
Sponsor Name:Lukács és Társa Gyógyszerkereskedelmi Betéti Társaság | ||
Full Title: A Phase II/III Adaptive, Seamless, Prospective, Randomized, Controlled, Parallel, Open Multicenter Study to Assess the Safety and Efficacy of Kék Lukács Ointment Compared to Standard Silver Sulfadi... | ||
Medical condition: Partial thickness (second-degree) burns. Total study target burn area: > 25 cm2 < 400 cm2 (or 2% of TBSA), and the burn therapy begun within 6-72 hours. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004165-13 | Sponsor Protocol Number: IJB-LBC-NEOCHECKRAY-2018 | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Neo-adjuvant chemotherapy combined with SBRT to the primary tumour +/- durvalumab (MEDI4736), +/- oleclumab in luminal B breast cancer: a phase ll randomized trial | |||||||||||||
Medical condition: Luminal B Breast Cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Ongoing) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003390-26 | Sponsor Protocol Number: BSG-12 | Start Date*: 2012-12-18 | |||||||||||
Sponsor Name:Birken AG | |||||||||||||
Full Title: Open, Blindly Evaluated, Prospective, Controlled, Randomized, Multicenter Phase III Clinical Trial to Compare Intra-individually the Efficacy and Tolerance of Oleogel-S10 versus Standard of Care in... | |||||||||||||
Medical condition: Split-Thickness Skin Graft Donor Sites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) GR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000777-23 | Sponsor Protocol Number: BSH-12 | Start Date*: 2012-07-05 | |||||||||||
Sponsor Name:Birken AG | |||||||||||||
Full Title: Open, Blindly Evaluated, Prospective, Controlled, Randomized, Multicenter Phase III Clinical Trial to Compare Intra-individually the Efficacy and Tolerance of Oleogel-S10 versus Standard of Care in... | |||||||||||||
Medical condition: Split-Thickness Skin Graft Donor Sites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) FI (Completed) AT (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002165-19 | Sponsor Protocol Number: 20177308 | Start Date*: 2019-05-10 |
Sponsor Name:Medical University Vienna | ||
Full Title: Neo-BCC trial: Neoadjuvant treatment of difficult to resect, locally advanced basal cell carcinoma (BCC) with Talimogene laherparepvec (T-VEC) | ||
Medical condition: Basal cell carcinoma (BCC) is the most common malignant neoplasm in fair skinned humans (Rubin et al., 2005). Over the last decades its incidence has increased (Chinem and Miot, 2011). Especially w... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003216-37 | Sponsor Protocol Number: n.a. | Start Date*: 2015-02-12 |
Sponsor Name: | ||
Full Title: Efficacy of Verapamil/ Verapamil-Kenacort injection versus Kenacort injection in Scar Treatment | ||
Medical condition: Hypertrophic and keloid scars are pathological scars as a result of dermal injury and exhibit exuberant, indefinite growth of collagen during wound healing. Hypertrophic and keloid scars often caus... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004209-98 | Sponsor Protocol Number: PEP 1.05 | Start Date*: 2005-12-08 |
Sponsor Name:Medical University Vienna, Department of Medicine III | ||
Full Title: The Vienna Prograf and Endothelial Progenitor Cell Study (Vienna PEP Study) | ||
Medical condition: Kidney Transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003498-16 | Sponsor Protocol Number: LOXO-TRK-15003 | Start Date*: 2017-02-10 | ||||||||||||||||||||||||||
Sponsor Name:Loxo Oncology Inc. | ||||||||||||||||||||||||||||
Full Title: A Phase 1/2 Study of the Oral TRK Inhibitor LOXO-101 in Pediatric Patients with Advanced Solid or Primary Central Nervous System Tumors | ||||||||||||||||||||||||||||
Medical condition: Central Nervous System Neoplasms and advanced solid tumors | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) DE (Restarted) SE (Trial now transitioned) DK (Trial now transitioned) FR (Ongoing) NL (Trial now transitioned) IE (Trial now transitioned) PL (Ongoing) IT (Ongoing) CZ (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004382-83 | Sponsor Protocol Number: ALA-AK-CT009 | Start Date*: 2016-06-09 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, observer-blind, intra-individual phase III study to evaluate the safety and efficacy of BF 200 ALA (Ameluz®) in combination with daylight-PDT (photodynamic therapy) in comparison with... | |||||||||||||
Medical condition: Actinic keratosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003241-42 | Sponsor Protocol Number: ALA-BCC-CT008 | Start Date*: 2013-12-23 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: A randomized, observer blind, multinational phase III study to evaluate the safety and efficacy of BF-200 ALA (Ameluz®) in comparison to Metvix® in the treatment of non-aggressive basal cell carcin... | |||||||||||||
Medical condition: Basal cell carcinoma (BCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006041-36 | Sponsor Protocol Number: PH-L19IL2TNFBASK-04/21 | Start Date*: 2022-08-31 | |||||||||||
Sponsor Name:PHILOGEN S.P.A. | |||||||||||||
Full Title: A phase II study of L19IL2/L19TNF in patients with skin cancers amenable to intralesional treatment | |||||||||||||
Medical condition: Patients with malignant tumors of the skin amenable to intratumoral injection, and in a curative or neoadjuvant or palliative intention, including: - Basal cell carcinoma (BCC) - Cutaneous squamous... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020380-20 | Sponsor Protocol Number: R331333-PAI2005/KF5503-59 | Start Date*: 2012-03-09 | |||||||||||
Sponsor Name:Janssen Research & Development, L.L.C. | |||||||||||||
Full Title: Open-Label Evaluation of the Pharmacokinetic Profile and Safety of Tapentadol Oral Solution for the Treatment of Postsurgical Pain in Children and Adolescents Aged From 6 to Less Than 18 Years | |||||||||||||
Medical condition: Pain | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002971-32 | Sponsor Protocol Number: PROICM2019-11PRA | Start Date*: 2020-07-27 |
Sponsor Name:Institut Regional du Cancer de Montpellier | ||
Full Title: A Double blind randomized phase III study of pravastatin vs placebo as primary prevention of severe subcutaneous breast fibrosis in hyper-radiosensitive identified patients with breast cancer | ||
Medical condition: Radio-induced fibrosis in breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
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