- Trials with a EudraCT protocol (382)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
382 result(s) found for: Reproductive surgery.
Displaying page 1 of 20.
EudraCT Number: 2008-002030-30 | Sponsor Protocol Number: AR_HSG_01-2008 | Start Date*: 2008-04-24 | |||||||||||
Sponsor Name:A.O. SAN GERARDO DI MONZA | |||||||||||||
Full Title: Impact of intraperitonael nebulization of local anesthetic on hypothermia and postoperative pain associated with laparoscopic surgery | |||||||||||||
Medical condition: Intra and post operatorive period | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002309-39 | Sponsor Protocol Number: 60/2011 | Start Date*: 2016-07-08 |
Sponsor Name:Osakidetza | ||
Full Title: EFFECTIVENESS OF ROPIVACAINE 0.1% INTRAPERITONEAL IN POSTOPERATIVE PAIN CONTROL IN GYNECOLOGIC LAPAROSCOPIC SURGERY " | ||
Medical condition: EFECTIVENESS OF ROPIVACAINE 0,1% FOR PAIN CONTROL AFTER LAPAROSCOPIC GYNECOLOGICAL SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001030-19 | Sponsor Protocol Number: FP2CLI003 | Start Date*: 2021-06-14 | |||||||||||
Sponsor Name:Faron Pharmaceuticals Ltd | |||||||||||||
Full Title: A Phase I/II Open Label Single Centre Trial to Assess the Safety, Tolerability and Efficacy of Single Dose Neoadjuvant Anti-CLEVER-1 Antibody Bexmarilimab in Localised Renal Cell and Colon Carcinoma | |||||||||||||
Medical condition: -Localized clear cell renal cell cancer -Colon adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000510-59 | Sponsor Protocol Number: 01012014 | Start Date*: 2014-08-11 | |||||||||||
Sponsor Name:Dept of Plastic Surgery, Breast Surgery & Burns | |||||||||||||
Full Title: Fat transplantation enriched with ex vivo expanded adipose-derived autologous mesenchymal stem cells in reconstruction of the breast. | |||||||||||||
Medical condition: The study will include participants with breast hypoplasia (International Classification of Diseases-10: DQ 838A). | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019830-29 | Sponsor Protocol Number: 3621 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Hopitaux Universitaires de Strasbourg | |||||||||||||
Full Title: Evaluation of the effects of CO2 insufflation on central body temperature and on postoperative pain in laparoscopic surgery | |||||||||||||
Medical condition: Elective videolaparoscopic hysterectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005140-18 | Sponsor Protocol Number: RAME-01 | Start Date*: 2015-11-12 | |||||||||||
Sponsor Name:ENTE OSPEDALIERO OSPEDALI GALLIERA | |||||||||||||
Full Title: Diagnostic and clinical value of fused 64CuCl2-PET/MRI in prostate cancer relapse. Comparison with multiparametric MRI (mMRI) and 18F-Choline-PET/MRI | |||||||||||||
Medical condition: Prostate cancer patients who showed biochemical relapse after surgery or first-line treatment with radiotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004018-15 | Sponsor Protocol Number: V710-003 | Start Date*: 2008-01-17 | ||||||||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | ||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Group-Sequential Study to Evaluate the Efficacy, Immunogenicity, and Safety of a Single Dose of Merck 0657nI Staphylococcus aureus Vaccine (V710) in Adult P... | ||||||||||||||||||
Medical condition: Staphylococcus aureus bacteremia Staphylococcus aureus mediastinitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) BE (Completed) ES (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) AT (Completed) FR (Prematurely Ended) IE (Prematurely Ended) DK (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005797-58 | Sponsor Protocol Number: 465 | Start Date*: 2013-04-19 | ||||||||||||||||
Sponsor Name:Kvinnokliniken, Universitetessjukhuset i Linköping, landstinget i Östergötland | ||||||||||||||||||
Full Title: Contraception after gastric bypass - part three How does gastric bypass affect the pharmacocinetics of oral desogestrel? | ||||||||||||||||||
Medical condition: We want to investigate how the pharmacocinetics changes for Cerazette in 14 fertile obese women after, compared to before, bariatric surgery in forms of gastric by pass. Mesures of serum concetrati... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004545-91 | Sponsor Protocol Number: 59874 | Start Date*: 2017-04-13 |
Sponsor Name:VU University Medical Center, department of reproductive Medicine | ||
Full Title: Continuous use of Oral contraceptives as an alternative for long term Pituitary down-regulation with GnRH agonist prior to IVF/ICSI in Endometriosis patients: a randomised controlled trial (COPIE t... | ||
Medical condition: The research population consists of women with surgically confirmed endometriosis ASRM stage III or IV or endometrioma on transvaginal ultrasound or MRI, scheduled for an IVF/ICSI treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004320-11 | Sponsor Protocol Number: 222013 | Start Date*: 2014-05-07 |
Sponsor Name:CARLOS SANTOS VILLAR | ||
Full Title: A ONE YEAR STUDY ON THE USE OF TRANEXAMIC ACID IN BENIGN PROSTATIC HYPERPLASIA SURGERY | ||
Medical condition: BENIGN PROSTATIC HYPERTROPHY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000134-34 | Sponsor Protocol Number: TEAM(B115UCS2019) | Start Date*: 2021-05-24 | |||||||||||
Sponsor Name:ENTE OSPEDALIERO OSPEDALI GALLIERA | |||||||||||||
Full Title: Time restricted Eating And Metformin (TEAM) in invasive breast cancer (IBC) or ductal carcinoma in situ (DCIS). A randomized, phase IIb, window of opportunity presurgical trial. | |||||||||||||
Medical condition: Luminal (ER+ve and/or PgR+ve >=1%) invasive breast cancer not candidate to neo - adjuvant chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004373-23 | Sponsor Protocol Number: ROV-BEM-2003-02 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:LABORATORIOS FARMACEUTICOS ROVI, S.A. | |||||||||||||
Full Title: MULTICENTRIC, RANDOMISED, DOUBLE BLIND, PLACEBO CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFICACY AND THE SAFETY OF THE PROPHYLAXIS WITH BEMIPARIN 3,500 IU/day FOR 28 DAYS COMPARED TO 8 DAYS, IN V... | |||||||||||||
Medical condition: VENOUS THROMBOEMBOLIC DISEASE IN PATIENTS UNDERGOING ONCOLOGICAL ABDOMINAL OR PELVIC SURGERY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004677-17 | Sponsor Protocol Number: 141022 | Start Date*: 2016-02-29 | ||||||||||||||||
Sponsor Name:Kvinnokliniken, Universitetssjukhuset i Linköping, Landstinget i Östergötland | ||||||||||||||||||
Full Title: Contraception after gastric bypass - part 4 How does gastric bypass affect the pharmacocinetics of oral levonorgestrel? | ||||||||||||||||||
Medical condition: We want to investigate if the pharmacocinetics of levonorgestrel differs in women who have had bariatric surgery compared to women who have not. Measures of serum concentrations of levonorgestrel w... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000535-33 | Sponsor Protocol Number: BCII_2015 | Start Date*: 2015-12-01 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Phase II, Open-Label Study to Evaluate Safety and Explore Efficacy of Escalating Doses of Bevacizumab-IRDye800CW as an Optical Imaging Agent to Detect Cancer Tissue Delineation During Tumor Resecti... | ||
Medical condition: Patients with breast cancer eligible for surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001036-22 | Sponsor Protocol Number: SOLTI-1114 | Start Date*: 2013-10-15 | |||||||||||
Sponsor Name:SOLTI | |||||||||||||
Full Title: PAM50 HER2-enriched phenotype as a predictor of early response to neoadjuvant lapatinib plus trastuzumab in Stage I to IIIA HER2-positive breast cancer | |||||||||||||
Medical condition: Untreated invasive breast carcinoma eligible for primary definitive surgery (Stage I-IIIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005112-17 | Sponsor Protocol Number: IRFMN-BRC-7103 | Start Date*: 2017-07-11 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: Multicenter, randomized, phase II study of neoadjuvant chemotherapy associated or not with zoledronate and atorvastatin in triple negative breast cancers - YAPPETIZER Study | |||||||||||||
Medical condition: Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004302-63 | Sponsor Protocol Number: CLI20001/Lita005 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:Litaphar Laboratorios S.L. | |||||||||||||
Full Title: A multi-centre, open-label, single-arm study assessing the safety and efficacy of 5 mg of mifepristone for the treatment of endometriosis in reproductive-age women during two treatment cycles of 24... | |||||||||||||
Medical condition: endometriosis in reproductive-age | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007988-16 | Sponsor Protocol Number: GICNO08.002 | Start Date*: 2009-05-08 |
Sponsor Name:OSPEDALE S. RAFFAELE | ||
Full Title: Imatinib piu` idrossiurea nel trattamento dei meningiomi recidivati o in progressione: studio randomizzato di fase II. | ||
Medical condition: patients affected by recurrent or progressive meningiomas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010786-22 | Sponsor Protocol Number: arom09 | Start Date*: 2009-03-03 | |||||||||||
Sponsor Name:IST - ISTITUTO NAZIONALE PER LA RICERCA SUL CANCRO | |||||||||||||
Full Title: Open label, phase III, multicentric randomised trial, comparing five years of treatment with a non steroidal aromatase inhibitor, either anastrozole or letrozole, versus switching after 2-3 years t... | |||||||||||||
Medical condition: post menopausal women with hormone-receptor positive early stage breast cancer, surgically removed | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005698-30 | Sponsor Protocol Number: 12-051 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Clinical Trial Center Aachen | |||||||||||||
Full Title: Impact of Xenon-anaesthesia on the renal function after partial nephrectomy - PaNeX: Partial Nephrectomy under Xenon | |||||||||||||
Medical condition: renal function after partial nephrectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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