- Trials with a EudraCT protocol (214)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
214 result(s) found for: Rectal administration.
Displaying page 1 of 11.
EudraCT Number: 2009-011325-14 | Sponsor Protocol Number: 09-001 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:Cliniques Universitaires Saint-Luc | |||||||||||||
Full Title: Phase II Study of Preoperative Panitumumab and External Beam Radiotherapy in Patients with Locally Advanced Rectal Cancer | |||||||||||||
Medical condition: Locally advanced adenocarcinoma of the rectum (T3 - T4 and/or N+ M0), previously untreated and non metastatic disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000876-40 | Sponsor Protocol Number: IJB-REGINA-2020 | Start Date*: 2021-03-09 | ||||||||||||||||
Sponsor Name:Institut Jules Bordet | ||||||||||||||||||
Full Title: A phase II trial of neoadjuvant REGorafenib in combination with nIvolumab and short-course radiotherapy iN stage II-III rectAl cancer | ||||||||||||||||||
Medical condition: rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000770-30 | Sponsor Protocol Number: IRST154.01 | Start Date*: 2013-07-10 | |||||||||||
Sponsor Name:IRCCS ISTITUTO SCIENTIFICO ROMAGNOLO PER LO | |||||||||||||
Full Title: Phase II study of up-front chemotherapy and neo-adjuvant short-course radiotherapy for resectable rectal carcinoma | |||||||||||||
Medical condition: resectable rectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011753-41 | Sponsor Protocol Number: 0902-127 | Start Date*: 2010-12-23 |
Sponsor Name:Neonatal intensive care unit, VU medical center Amsterdam | ||
Full Title: Pain treatment of newborns: paracetamol rectal versus intraveneous administration, an open randomised clinical trial. | ||
Medical condition: Pain treatment of neonates and premature neonates. | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005011-17 | Sponsor Protocol Number: 7TNANO1 | Start Date*: 2015-02-24 |
Sponsor Name:Radboudumc | ||
Full Title: Nano MRI on 7 Tesla: A technical validation study in rectal and breast cancer | ||
Medical condition: Lymph node metastases in rectal cancer, breast cancer and cancer in general | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2013-005108-32 | Sponsor Protocol Number: BP29262 | Start Date*: 2014-08-04 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A PHASE II, MULTICENTER, RANDOMIZED, DOUBLE-BLIND STUDY TO EVALUATE THE EFFICACY AND SAFETY OF RO5520985 (VANUCIZUMAB) PLUS FOLFOX VERSUS BEVACIZUMAB PLUS FOLFOX IN PATIENTS WITH PREVIOUSLY UNTREA... | |||||||||||||||||||||||
Medical condition: Patients with cancer of the colon or rectum where the tumor has already spread to other organs(s), | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Prematurely Ended) ES (Completed) IT (Completed) GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002141-42 | Sponsor Protocol Number: NL73593 | Start Date*: 2020-07-03 |
Sponsor Name:Catharina Hospital | ||
Full Title: Multicentre, open-label, randomised, controlled, parallel arms clinical trial of induction chemotherapy followed by chemoradiotherapy versus chemoradiotherapy alone as neoadjuvant treatment for loc... | ||
Medical condition: Locally recurrent rectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) PT (Trial now transitioned) NO (Trial now transitioned) BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023538-22 | Sponsor Protocol Number: LY107 | Start Date*: 2011-08-30 |
Sponsor Name:Lipid Pharmaceuticals | ||
Full Title: Lýsi sem hægðalyf fyrir börn | ||
Medical condition: The primary objective of this trial is to investigate the laxative effect of Lysisstílar (Free Fatty Acids suppositories) as compared to Klyx. Participants are children aged 1 year old to 17 year... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002425-35 | Sponsor Protocol Number: NL2014-002425-35/SpartacusBrindisi | Start Date*: 2015-07-20 |
Sponsor Name:National Poisons Information Center, University Medical Center Utrecht | ||
Full Title: A Single Centered, Prospective, Open-labeled, Pharmacokinetic Pilot Study of Tacrolimus Administration via Rectiole | ||
Medical condition: Heart and lung transplantation patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000997-13 | Sponsor Protocol Number: HEHDZ01 | Start Date*: 2018-03-02 | |||||||||||
Sponsor Name:Center for Perioperative Optimization, Department of Surgery, Herlev Hospital | |||||||||||||
Full Title: Pharmacokinetics of intravenous, rectal, intravesical, vaginal, and transdermal administration of exogenous melatonin in healthy female volunteers: a crossover study | |||||||||||||
Medical condition: Pharmacokinetics of melatonin | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024354-11 | Sponsor Protocol Number: ABCSGR05 | Start Date*: 2011-03-03 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: Preoperative induction chemotherapy in combination with Bevacizumab followed by combined chemoradiotherapy in locally advanced rectal cancer with high risk of recurrence- phase II pilot study with ... | ||
Medical condition: locally advanced rectal cancer with high risk of recurrence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003831-21 | Sponsor Protocol Number: 2277/2007 | Start Date*: 2007-07-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: PHARMACOKINETIC PERSPECTIVE STUDY IN COLORECTAL CANCER PATIENTS AND CANDIDATE FOR FLUOROPYRIMIDINE THERAPY: 5-FLUORO TEST | |||||||||||||
Medical condition: Colo-rectal adenocarcinoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004040-36 | Sponsor Protocol Number: CE01-302 | Start Date*: 2014-10-10 |
Sponsor Name:Cempra Pharmaceuticals, Inc. | ||
Full Title: A Study to Evaluate the Efficacy and Safety of Oral Solithromycin Compared to Intramuscular Ceftriaxone Plus Oral Azithromycin in the Treatment of Patients With Gonorrhea (SOLITAIRE-U). | ||
Medical condition: gonorrhoea | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2015-001942-28 | Sponsor Protocol Number: APD334-003 | Start Date*: 2015-12-10 | |||||||||||
Sponsor Name:Arena Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Center Study to Investigate the Safety and Efficacy of APD334 in Patients with Moderately to Severely Active Ulcerativ... | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) ES (Completed) DE (Completed) LV (Completed) HU (Completed) LT (Completed) FR (Completed) PL (Completed) BG (Completed) BE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009863-75 | Sponsor Protocol Number: CEAEP_2009-05-29 | Start Date*: 2009-08-26 | |||||||||||
Sponsor Name:Karolinska Institutet/ Hospital | |||||||||||||
Full Title: El-porCEA: Assessment of safety and immunogenicity of intradermal electroporation of tetwtCEA DNA in patients with colorectal cancer. | |||||||||||||
Medical condition: Colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005547-27 | Sponsor Protocol Number: GO28074 | Start Date*: 2012-10-24 | |||||||||||||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||||||||||||
Full Title: A PHASE II, MULTICENTER, OPEN-LABEL, RANDOMIZED STUDY EVALUATING THE EFFICACY AND SAFETY OF FOLFIRI + MEHD7945A VERSUS FOLFIRI + CETUXIMAB IN SECOND LINE IN PATIENTS WITH KRAS WILD-TYPE METASTATIC ... | |||||||||||||||||||||||
Medical condition: Colorectal cancer that does not carry mutation in the KRAS gene | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001561-28 | Sponsor Protocol Number: HES08 | Start Date*: 2008-07-21 |
Sponsor Name:Klinik für Anästhesiologie und Operative Intensivmedizin Klinikum Ludwigshafen | ||
Full Title: Influence of perioperative HES 130/04 adminstration on postoperative complications: A prospective randomized trial in patients undergoing colorectal surgery. | ||
Medical condition: Adult patients (>18 years) of both gender undergoing elective colorectal surgery (hemicolectomy left/right, sigmoid colectomy, rectal resection/amputation) without concomitant resection of liver me... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006779-41 | Sponsor Protocol Number: CAR-GR | Start Date*: 2022-10-26 |
Sponsor Name:FUNDACIÓN FLS DE LUCHA CONTRA EL SIDA, LAS ENFERMEDADES INFECCIOSAS Y LA PROMOCIÓN DE LA SALUD Y LA CIENCIA | ||
Full Title: HIV-1 RNA suppression and drug concentrations in semen, cervicovaginal fluid and rectum in HIV-1 infected individuals receiving intramuscular long-acting cabotegravir plus rilpivirine (“CAR-GR Study) | ||
Medical condition: HIV infected individuals | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002593-89 | Sponsor Protocol Number: TV48574-IMM-20038 | Start Date*: 2023-03-15 | ||||||||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | ||||||||||||||||||
Full Title: A 24-Week, Phase 2b, Randomized, Double-Blind Long-Term Extension Study to Evaluate Pharmacokinetics, Efficacy Safety, and Tolerability of TEV-48574 in Adult Patients with Moderate to Severe Ulcera... | ||||||||||||||||||
Medical condition: Moderate to severe Ulcerative colitis or moderate to severe Crohn's disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) CZ (Trial now transitioned) SK (Trial now transitioned) IT (Trial now transitioned) FR (Completed) BG (Trial now transitioned) AT (Trial now transitioned) HU (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013756-79 | Sponsor Protocol Number: VECTOX | Start Date*: 2010-09-28 | ||||||||||||||||
Sponsor Name:Anticancer Informing "Me Gnosi Nika" | ||||||||||||||||||
Full Title: VECTIBIX PLUS OXALIPLATIN-BASED ADJUVANT TREATMENT OF RECTAL CANCER | ||||||||||||||||||
Medical condition: Rectal cancer stage 2-3 includes neoadjuvant chemo radiation, followed by resection, followed by adjuvant chemotherapy. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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