- Trials with a EudraCT protocol (5,386)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    5,386 result(s) found for: Pregnancy rate.
                    
                
			
   			
		
		Displaying page 1 of 270.
	
	
	| EudraCT Number: 2018-001014-15 | Sponsor Protocol Number: S61372 | Start Date*: 2018-06-26 | 
| Sponsor Name:university hospital leuven | ||
| Full Title: Frozen-thawed embryo transfer in a natural versus artificial cycle: a randomized clinical trial | ||
| Medical condition: Patients with subfertility having frozen embryos after in vitro fertilization (IVF) or intracytoplasmatic sperm injection (ICSI) | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004112-10 | Sponsor Protocol Number: PROTECTA | Start Date*: 2020-12-16 | 
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Randomized controlled trial comparing micronized progesterone (Amelgen ®) 400 mg BID versus 400 mg TID for luteal support in artificial vitrified/warmed single blastocyst transfer cycles with low p... | ||
| Medical condition: Patients who undergo artificial vitrified/warmed single blastocyst transfer cycles with low progesterone (defined as <10mcg/l) on day of embryo transfer. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000689-13 | Sponsor Protocol Number: HRT1vs2week.2018 | Start Date*: 2018-07-11 | |||||||||||
| Sponsor Name:University hospital Brussel | |||||||||||||
| Full Title: Clinical pregnancy rate for frozen embryo transfer with HRT: a pilot study comparing 1 versus 2 weeks of treatment | |||||||||||||
| Medical condition: Subfertility in need of IVF and IVF-ICSI treatment | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003484-56 | Sponsor Protocol Number: BOLDOS-18 | Start Date*: 2019-12-26 | |||||||||||
| Sponsor Name:Miguel Caballero Campo | |||||||||||||
| Full Title: Efficacy of corifolitropin alfa in double ovarian stimulation compared with two conventional ovarian stimulation cycles for embryo accmulation in low responder patients. Multicenter randomized cont... | |||||||||||||
| Medical condition: Infertility in patients requiring in vitro fertilization treatment with poor ovarian response profile, defined by Bologna Criteria. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001984-53 | Sponsor Protocol Number: ETHIG II | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
| Full Title: Effectiveness of Dalteparin Therapy as Intervention in recurrent pregnancy loss | |||||||||||||
| Medical condition: Pregnant women with a history of recurrent pregnancy loss, defined as: - 2 or more early (< 12 weeks of gestation) pregnancy losses or - 1 or more late (> 12 weeks of gestation) pregnancy loss | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002032-84 | Sponsor Protocol Number: ELYS-CS01 | Start Date*: 2019-10-31 | |||||||||||
| Sponsor Name:Disphar International B.V | |||||||||||||
| Full Title: Evaluating the Use of a Progesterone Receptor Modulator for Cervical Ripening at Full Term Pregnancy – a Randomized, Double-blind , placebo controlled Study (LUCYNA) | |||||||||||||
| Medical condition: Full-term pregnancy women at week 40 + 5 of gestation with intact membranes, the first delivery, singleton physiological pregnancy | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002040-24 | Sponsor Protocol Number: FI028.DEX001.2019 | Start Date*: 2020-04-14 | 
| Sponsor Name:Dextra fertility clinic [...] | ||
| Full Title: Iron defiency as an ignored cause of infertility | ||
| Medical condition: Infertility | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-001747-69 | Sponsor Protocol Number: GEMII-1 | Start Date*: 2011-10-28 | |||||||||||
| Sponsor Name:Monash University [...] | |||||||||||||
| Full Title: Combination gefitinib and methotrexate to treat ectopic pregnancies II | |||||||||||||
| Medical condition: Ectopic pregnancy or pregnancy of unknown location. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003778-29 | Sponsor Protocol Number: CTU/2013/064 | Start Date*: 2014-01-30 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Combined Multi-Marker Screening and Randomised Patient Treatment with Aspirin for Evidence-based Pre-eclampsia Prevention | |||||||||||||
| Medical condition: Pre-eclampsia | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) IT (Completed) BE (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004491-17 | Sponsor Protocol Number: REMODEL | Start Date*: 2021-03-31 | 
| Sponsor Name:UZ Brussel | ||
| Full Title: Dydrogesterone versus micronized vaginal progesterone (MVP) for luteal phase support (LPS) in hormone replacement therapy (HRT) frozen embryo transfer (FET) cycles. | ||
| Medical condition: progesterone as luteal phase supplementation in frozen embryo transfer cycles | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002897-27 | Sponsor Protocol Number: 18E-Prg06 | Start Date*: 2018-12-21 | |||||||||||
| Sponsor Name:IBSA, Institut Biochimique, S.A. | |||||||||||||
| Full Title: A proof of concept, randomized, controlled clinical trial to assess the efficacy of subcutaneous progesterone (Prolutex) versus vaginal proges-terone (Progeffik) for endometrial preparation in wome... | |||||||||||||
| Medical condition: Infertility. Assisted Reproductive Tecniques. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-001045-21 | Sponsor Protocol Number: FSD-MIC-2022-03 | Start Date*: 2023-04-10 | 
| Sponsor Name:FUNDACION SANTIAGO DEXEUS FONT | ||
| Full Title: A Phase III randomized controlled trial comparing the efficacy, safety and tolerability of two formulations of vaginal micronized progesterone. | ||
| Medical condition: Infertility | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000993-32 | Sponsor Protocol Number: S55300 | Start Date*: 2013-05-07 | ||||||||||||||||
| Sponsor Name:University Hospital Leuven | ||||||||||||||||||
| Full Title: Does prolonged GnRH downregulation prior to ART improve the clinical pregnancy rate in postoperative endometriosis patients? A RCT | ||||||||||||||||||
| Medical condition: endometriosis, subfertility | ||||||||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-000001-25 | Sponsor Protocol Number: OXO-001-201 | Start Date*: 2021-08-06 | 
| Sponsor Name:Oxolife S.L. | ||
| Full Title: A phase II, randomised, double-blind, parallel-group, placebo-controlled trial to assess the ongoing pregnancy rate with OXO-001 (200 mg, 300 mg) or placebo at 10 weeks following fresh single blast... | ||
| Medical condition: Infertility treatment and fertility enhancer in women undergoing assisted reproductive techniques or natural reproduction | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: PL (Completed) ES (Ongoing) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000084-40 | Sponsor Protocol Number: NT-05 | Start Date*: 2014-04-07 | |||||||||||
| Sponsor Name:Nora Therapeutics, Inc. | |||||||||||||
| Full Title: A randomized, double blind, multi-center, placebo-controlled study to evaluate the efficacy, safety, and tolerability of NT100 in pregnant women with a history of unexplained recurrent pregnancy lo... | |||||||||||||
| Medical condition: Unexplained recurrent pregnancy loss. A distinct disorder from sporadic pregnancy loss and is characterized by the loss of multiple pregnancies | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-001323-64 | Sponsor Protocol Number: 7/2008/O/Sper | Start Date*: 2008-03-12 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: PHASE III DOUBLE BLIND PLACEBO CONTROLLED RANDOMIZED STUDY ON THE EFFICACY OF URSODEOXYCHOLIC ACID FOR THE TREATMENT OF INTRAHEPATIC CHOLESTASIS OF PREGNANCY | |||||||||||||
| Medical condition: INTRAHEPATIC CHOLESTASIS OF PREGNANCY | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000599-33 | Sponsor Protocol Number: LWH0646 | Start Date*: 2006-08-21 | 
| Sponsor Name:Liverpool Women's NHS Foundation Trust | ||
| Full Title: Duration of luteal phase support with progesterone pessaries to improve the success rate in assisted reproduction cycles. A prospective randomised control trial. | ||
| Medical condition: Women undergoing assisted conception | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000811-26 | Sponsor Protocol Number: STOPPRE | Start Date*: 2018-09-19 | |||||||||||
| Sponsor Name:Vall D'Hebron Institut de Recerca (VHIR) | |||||||||||||
| Full Title: A phase III, multicentric, Randomized, open-label, parallel-group clinical trial to detect false positives from first-trimester preeclampsia screening (StopPRE) at the second-trimester of pregnancy. | |||||||||||||
| Medical condition: First-trimester pre-eclampsia patients | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001950-16 | Sponsor Protocol Number: ISI-2015-1 | Start Date*: 2017-03-03 | 
| Sponsor Name:Isifer AB | ||
| Full Title: A randomized, double blind, controlled, parallel group, multi-centre phase II clinical study of lidocaine pertubation as a treatment for couples with unexplained infertility | ||
| Medical condition: Unexplained infertility | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001124-20 | Sponsor Protocol Number: PCOS-5 | Start Date*: 2005-04-18 | 
| Sponsor Name:Sigrun Kjøtrød | ||
| Full Title: Metformin treatment before IVF/ICSI in normal weight women with polycystic ovarian syndrome. A European, prospective, randomised, double blind, multicenter study. | ||
| Medical condition: Polycystic ovary syndrome (PCOS) is a disorder characterized by polycystic ovaries, oligo-amenorrhea and hyperandrogenism. It is the most common endocrine disorder in women of fertile age. PCOS wom... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DK (Completed) SE (Completed) FI (Completed) GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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