- Trials with a EudraCT protocol (687)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
687 result(s) found for: Paraffin.
Displaying page 1 of 35.
| EudraCT Number: 2010-022842-26 | Sponsor Protocol Number: UMCNONCO201004 | Start Date*: 2010-11-25 |
| Sponsor Name:University Medical Centre Nijmegen | ||
| Full Title: Autophagy inhibition using hydrochloroquine in breast cancer patients: a pilot study | ||
| Medical condition: proven invasive adenocarcinoma of the breast | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004039-19 | Sponsor Protocol Number: GEIS-51 | Start Date*: 2017-03-23 |
| Sponsor Name:Grupo Español de Investigación en Sarcomas (GEIS) | ||
| Full Title: Phase II multicenter trial of palbociclib in second line of advanced sarcomas with CDK4 overexpression. | ||
| Medical condition: Patients with advanced soft tissue sarcomas and osteosarcomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002081-12 | Sponsor Protocol Number: AHV-18-A | Start Date*: 2019-12-19 |
| Sponsor Name:Amryt Research Ltd. | ||
| Full Title: An exploratory randomized, intra-individual controlled trial of the cutaneous healing properties of Petrolatum versus the vehicle for Oleogel-S10 versus no treatment when applied topically to me... | ||
| Medical condition: Not applicable, as healthy volunteers will be recruited, who will receive mechanically induced partial thickness wounds. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002358-26 | Sponsor Protocol Number: AHV-18-B | Start Date*: 2020-09-29 |
| Sponsor Name:Amryt Research Ltd. | ||
| Full Title: A randomised, intra-individual controlled trial of the cutaneous healing properties of petrolatum versus the vehicle for Oleogel-S10 when applied topically to mechanically induced partial thickness... | ||
| Medical condition: Not applicable, as healthy volunteers will be recruited, who will receive mechanically induced partial thickness wounds. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001556-67 | Sponsor Protocol Number: derhill2017/1 | Start Date*: 2017-05-17 | |||||||||||
| Sponsor Name:UZ Brussel | |||||||||||||
| Full Title: The effect of emollients on pruritus in psoriasis | |||||||||||||
| Medical condition: Psoriasis is traditionally considered a non-itchy skin disease. It seems that itch is an underestimated, and therefore undertreated aspect of psoriasis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003295-37 | Sponsor Protocol Number: V00034CR3121B | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
| Full Title: Efficacy of the V0034CR01B emollient on xerosis in children with atopic dermatitis. Randomised, vehicle-controlled, parallel-groups, double-blind study with an open label extension | |||||||||||||
| Medical condition: xerosis in children with atopic dermatitis | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) EE (Completed) LT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002264-27 | Sponsor Protocol Number: ENGOT-ov54/Swiss-GO-2/MATAO | Start Date*: 2021-03-17 |
| Sponsor Name:Swiss GO Trial Group | ||
| Full Title: MAintenance Therapy with Aromatase inhibitor in epithelial Ovarian cancer: a randomized double-blinded placebo-controlled multi-center phase III Trial (ENGOT-ov54/Swiss-GO-2/MATAO) including LOGOS ... | ||
| Medical condition: Patients with low and high grade serous and endometrioid ovarian cancer patients. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Trial now transitioned) DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002201-31 | Sponsor Protocol Number: V00034 CR 308 (ORF) | Start Date*: 2006-11-14 |
| Sponsor Name:ORFAGEN | ||
| Full Title: Long-term efficacy and safety of V0034 CR 01B cream in patients with moderate-to-severe uremic xerosis. | ||
| Medical condition: Palliative treatment of uremic xerosis of moderate to severe intensity. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) GR (Prematurely Ended) HU (Completed) CZ (Prematurely Ended) LV (Prematurely Ended) | ||
| Trial results: Removed from public view | ||
| EudraCT Number: 2013-004139-62 | Sponsor Protocol Number: CRAD001JES13 | Start Date*: 2014-01-02 | |||||||||||
| Sponsor Name:Novartis Farmacéutica S. A. | |||||||||||||
| Full Title: A pilot open-label, phase II, single-arm study to evaluate the association of biomarkers of hormonal resistance and the mTOR pathway with the clinical efficacy of everolimus plus letrozole in the f... | |||||||||||||
| Medical condition: Estrogen receptor or progesterone receptor positive locally advanced or metastatic breast cancer in postmenopausal women | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004621-24 | Sponsor Protocol Number: V00034CR3131B | Start Date*: 2013-02-04 | |||||||||||
| Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
| Full Title: Emollients in the management of atopic dermatitis in children: prevention of flares. | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: LT (Completed) EE (Completed) PL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-000877-30 | Sponsor Protocol Number: SK0608 | Start Date*: 2006-09-08 |
| Sponsor Name:Reckitt Benckiser Healthcare International | ||
| Full Title: A 6 week, multi centre study to evaluate the efficacy and safety of E45 complete emollient therapy and E45 itch relief cream in the treatment of mild to moderate atopic eczema compared to a patient... | ||
| Medical condition: Atopic Eczema | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002909-25 | Sponsor Protocol Number: 74310 | Start Date*: 2020-10-21 |
| Sponsor Name:Amsterdam University Medical Centers | ||
| Full Title: Blood-borne assessment of stromal activation in esophageal adenocarcinoma to guide tocilizumab therapy: a randomized phase II proof-of-concept study | ||
| Medical condition: oesophageal adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001509-26 | Sponsor Protocol Number: DESG-01 | Start Date*: 2006-10-11 |
| Sponsor Name:Dermal Laboratories Limited | ||
| Full Title: An open evaluation of an emollient shower gel for dry skin conditions. | ||
| Medical condition: Dry or chapped skin conditions which may also be pruritic (itchy) or inflamed e.g. eczema, psoriasis, elderly pruritus and dermatitis. | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-004762-33 | Sponsor Protocol Number: MOPAD | Start Date*: 2019-12-19 |
| Sponsor Name:InfectoPharm Arzneimittel und Consilium GmbH | ||
| Full Title: Prospektive, randomisierte, Nicht-Behandlungs-kontrollierte, Untersucher-verblindete, Multizenter-Studie zur Prophylaxe von frühkindlichen Symptomen der Atopischen Dermatitis bei Hochrisiko-Kindern... | ||
| Medical condition: Prävention der frühkindlichen Symptome der Atopischen Dermatitis bei Hochrisiko-Kindern | ||
| Disease: | ||
| Population Age: Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-016571-30 | Sponsor Protocol Number: DERL-02 | Start Date*: 2010-02-01 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to determine the effects on stratum corneum of a clinical hand cleansing protocol comparing two antiseptic hand washes, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: No medical condition is to be investigated, as such. We are looking to avoid occupational hand dermatitis in healthcare professionals, simulated using a repeat hand wash cleansing protocol in heal... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000333-22 | Sponsor Protocol Number: DERL-01 | Start Date*: 2008-04-30 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: A study to compare the effects on stratum corneum of two medical hand wash formulations, using non-invasive instrumental methods in human volunteers. | ||
| Medical condition: The study is a healthy volunteer study. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016572-78 | Sponsor Protocol Number: DEBE-01 | Start Date*: 2010-04-27 |
| Sponsor Name:Dermal Laboratories Ltd | ||
| Full Title: Arm immersion test to compare the skin effects of routine bathing with and without the use of an emollient bath additive. | ||
| Medical condition: Eczema sufferers with dry skin. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-003348-31 | Sponsor Protocol Number: 2007/311 | Start Date*: 2008-05-15 |
| Sponsor Name:Department of Woman and Child health, Karolinska University Hospital | ||
| Full Title: Progesterone at imminent premature birth Progesteron vid hotande förtidsbörd | ||
| Medical condition: In this randomised, placebo-controlled pilot study the treatment group (n=30) will recieve a daily application of vaginal gel containing progesterone 90 mg/dose (Crinone, Seronomerck) until rupture... | ||
| Disease: | ||
| Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Under 18, Adults | Gender: Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-021658-21 | Sponsor Protocol Number: HN10/01 | Start Date*: 2010-09-27 |
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||
| Full Title: Phase II study of preoperative TPF chemotherapy in locally advanced resectable oral cavity squamous cell cancer in order to improve the rate of pathological complete response | ||
| Medical condition: oral cavity cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000707-34 | Sponsor Protocol Number: 2316 | Start Date*: 2011-11-08 |
| Sponsor Name:The Newcastle upon Tyne Hospitals NHS Trust | ||
| Full Title: The induction of apoptosis by anti-psoriatic treatments | ||
| Medical condition: Psoriasis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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