35 results match your criteria: "IVF centers Prof. Zech[Affiliation]"
Obstet Gynecol Sci
May 2023
Department of Biology, Laboratory of Molecular Genetic Physiopathology and Biotechnology, Ain Chock Faculty of Sciences, HASSAN II University Casablanca, Morocco.
Objective: To compare the degree of efficiency between density gradient centrifugation (DGC) method and an extended horizontal swim-up (SU) method.
Methods: A total of 97 couples undergoing in vitro fertilization were enrolled in the study. Semen samples were divided into three aliquots and treated using DGC, extended horizontal SU, and combined methods.
Reprod Biol Endocrinol
February 2021
The Fertility Clinic, Ringhospital, University Hospital of Copenhagen, Copenhagen, Denmark.
Reprod Biomed Online
July 2018
IVF Centers Prof. Zech - Bregenz, Roemerstrasse 2, Bregenz, 6900, Austria.
J Assist Reprod Genet
June 2018
Centre de Procréation Médicalement Assistée - ULiège, Centre Hospitalier Universitaire de Liège, Liège, Belgium.
Purpose: The aim of this study was to compare the effect of the deselection of spermatozoa presenting vacuole-like structures using IMSI (intracytoplasmic morphologically selected sperm injection) with ICSI (intracytoplasmic sperm injection) by means of neonatal outcomes.
Methods: In a retrospective two-center analysis, a total of 848 successful IMSI or ICSI cycles ending with a live birth, induced abortion, or intrauterine fetal death (IUFD) were included.
Results: The IMSI and ICSI groups included 332 and 655 babies or fetuses, respectively.
Ultrasound Obstet Gynecol
January 2018
IVF Centers Prof. Zech - Bregenz, Bregenz, Austria.
Objective: To analyze oocyte competence in gonadotropin-releasing hormone agonist (GnRHa) stimulation cycles with regard to maturity, fertilization and blastocyst rate, as well as clinical outcome (pregnancy and live-birth rate), in relation to follicular volume, measured by three-dimensional transvaginal sonography (3D-TVS), and follicular fluid composition.
Methods: This was a prospective single-center study conducted between June 2012 and June 2014, including 118 ovum pick-ups with subsequent embryo transfer. Ovarian stimulation was performed using the GnRHa long protocol.
Fertil Steril
November 2016
IAKENTRO Advanced Medical Center, Thessaloniki, Greece.
Objective: To evaluate whether is possible to vitrify oocytes in an aseptic (hermetically closed) fashion and maintain clinical results comparable with those of fresh oocytes.
Design: Prospective, observational, cohort, noninferiority trial.
Setting: Private in vitro fertilization center.
Hum Reprod
August 2016
IVF Centers Prof. Zech - Bregenz, Römerstrasse 2, A-6900 Bregenz, Austria Centre Hospitalier Inter Régional Edith Cavell (CHIREC), Braine-l'alleud, Bruxelles, Belgium.
Study Question: How do live birth rates (LBRs), following fresh and vitrified/warmed embryo transfer, compare according to morphological grade, developmental stage and culturing strategy of human blastocysts in vitro?
Summary Answer: Equivalent LBRs were obtained after fresh embryo transfer and after vitrified/warmed embryo transfer of blastocysts of top or non-top quality, while vitrification after prolonged embryo culture of blastocysts with delayed development had a positive impact on LBR.
What Is Known Already: Blastocyst morphology correlates with clinical outcome; however, few data are available on vitrified/warmed embryo transfer using non-top quality blastocysts. The aim of this study was to determine clinical outcomes of non-top quality blastocysts and blastocysts with delayed development that underwent vitrified/warmed embryo transfer.
J Assist Reprod Genet
November 2015
IVF Centers Prof. Zech-Bregenz, Römerstrasse 2, 6900, Bregenz, Austria.
Purpose: Various time-lapse studies have postulated embryo selection criteria based on early morphokinetic markers. However, late paternal effects are mostly not visible before embryonic genome activation. The primary objective of this retrospective study was to investigate whether those early morphokinetic algorithms investigated by time-lapse imaging are reliable enough to allow for the accurate selection of those embryos that develop into blastocysts, while of course taking into account the correlation with the type of injected spermatozoa.
View Article and Find Full Text PDFReprod Biol Endocrinol
July 2015
IVF Centers Prof. Zech, Römerstrasse 2, 6900, Bregenz, Austria.
Background: Successful embryo implantation depends on a well-timed maternal-embryonic crosstalk. Human chorionic gonadotropin (hCG) secreted by the embryo is known to play a key role in this process and to trigger a complex signal transduction cascade allowing the apposition, attachment, and invasion of the embryo into the decidualized uterus. Production of hCG was reported to be dependent on blastocyst quality and several articles suggested that intrauterine hCG injection increases pregnancy and implantation rates in IVF patients.
View Article and Find Full Text PDFMinerva Ginecol
April 2015
IVF Centers Prof. Zech, Bregenz, Austria -
Conventional controlled ovarian stimulation (cCOS) can cause significant discomfort, including ovarian hyperstimulation syndrome (OHSS). Clearly, management of OHSS and poor responder patients requires new strategies to overcome these problems and facilitate the birth of a healthy child with the fewest stimulation cycles. Several alternative methods have been developed.
View Article and Find Full Text PDFEvid Based Complement Alternat Med
August 2014
Biomedical Centre, Faculty of Medicine in Pilsen, Charles University in Prague, 301 00 Pilsen, Czech Republic ; Department of Physiology, Faculty of Medicine in Pilsen, Charles University in Prague, 301 00 Pilsen, Czech Republic.
Propolis is a natural product that honeybees collect from various plants. It is known for its beneficial pharmacological effects. The aim of our study was to evaluate the impact of propolis on human sperm motility, mitochondrial respiratory activity, and membrane potential.
View Article and Find Full Text PDFJ Reprod Infertil
April 2014
IVF Centers Prof Zech, Bregenz, Austria.
Background: The complexity of assisted reproductive technology (ART) increased during the last decades. New scientific and medical findings as well as the statutory requirements for improving the safety and the outcome of ART were the main impetus for its development. While therapy planning is done and ART is used by the IVF centers, the medical support and monitoring of patients is conducted by referring gynecologists.
View Article and Find Full Text PDFTime-lapse imaging is increasingly applied as an adjunct to reproductive medicine. The gained information of the morphological and morphokinetic variables before the onset of transcription are supposed to be good predictors for the selection of the best embryo for transfer and are often seen in line with clinical outcomes. This retrospective case series investigated the outcome of transferred blastocysts that did not fulfil the proposed embryo scores at early cleavage or at later stages of development.
View Article and Find Full Text PDFHum Reprod
November 2013
IVF Centers Prof. Zech - Bregenz, Römerstrasse 2, 6900 Bregenz, Austria.
Study Question: Does the storage time of vitrified human blastocysts negatively impact their survival, the implantation potential of embryos or the malformation rate of babies born?
Summary Answer: There was no evidence that storage times of up to 6 years after vitrification (VIT) had a negative impact on blastocyst survival, the implantation potential of embryos or the malformation rate of babies born.
What Is Known Already: Although several thousand children have been born after blastocyst VIT, many aspects of this technique remain to be elucidated. New applications, such as fertility preservation, lead to long storage times of vitrified gametes or embryos but it remains to be determined if these vitrified embryos are stable over time.
Int J Vitam Nutr Res
December 2012
IVF Centers Prof Zech, Bregenz, Austria.
Background: This study aimed to investigate the influence of an oral antioxidative supplementation on sperm quality of in vitro fertilization (IVF) patients, as analyzed by sperm motility according to the WHO criteria and motile sperm organelle morphology examination (MSOME).
Methods: Semen samples were collected from 147 patients before undergoing an IVF/intracytoplasmic morphologically-selected sperm injection (IMSI) cycle and 2 - 12 months after an antioxidative supplementation. Semen analysis was evaluated according to WHO and MSOME criteria.
Arch Gynecol Obstet
December 2013
IVF Centers Prof. Zech-Bregenz, Roemerstrasse 2, 6900, Bregenz, Austria,
J Assist Reprod Genet
August 2013
IVF Centers Prof. Zech-Bregenz, Römerstrasse 2, 6900, Bregenz, Austria,
Study Question: What is the intracellular concentration of cryoprotectant (ICCP) in mouse zygotes during vitrification (VIT) and slow-freezing (SLF) cryopreservation procedures?
Summary Answer: Contrary to common beliefs, it was observed that the ICCP in vitrified zygotes is lower than after SLF, although the solutions used in VIT contain higher concentrations of cryoprotectants (CPs).
What Is Known Already: To reduce the likelihood of intracellular ice crystal formation, which has detrimental effects on cell organelles and membranes, VIT was introduced as an alternative to SLF to cryopreserve embryos and gametes. Combined with high cooling and warming rates, the use of high concentrations of CPs favours an intracellular environment that supports and maintains the transition from a liquid to a solid glass-like state devoid of crystals.
Since the introduction of the motile sperm organelle morphology examination, there has been increasing recognition of the fact that the presence of large nuclear vacuoles might have deleterious effects on embryo development. Nevertheless, one fundamental question still being debated is whether specific in-vitro conditions during the handling of semen have an impact on vacuole formation. This study's objective was to analyse whether incubation temperature (20, 37°C) or oxidative stress stimulates the formation of nuclear vacuoles.
View Article and Find Full Text PDFReprod Biol Endocrinol
December 2012
IVF Centers Prof Zech-Bregenz, Roemerstrasse 2, Bregenz 6900, Austria.
Background: Poor sperm quality can negatively affect embryonic development and IVF outcome. This study is aimed at investigating the influence of various lifestyle factors on semen quality according to MSOME (motile sperm organelle morphology examination) criteria.
Methods: 1683 male patients undergoing assisted reproductive technologies (ART) in our clinic were surveyed about their age, BMI (body mass index), ejaculation frequency, nutrition, sports, sleeping habits and social behavior.
Reprod Biomed Online
December 2012
IVF Centers Prof. Zech-Bregenz, Römerstrasse 2, 6900 Bregenz, Austria.
In some IVF cycles, no fresh embryo transfer in the stimulated cycle is advisable. The cryopreservation of zygotes and the transfer of blastocysts in a cryo-embryo transfer is an option to circumvent an inadequate uterine environment due to risk of ovarian hyperstimulation syndrome, inappropriate endometrium build up, endometrial polyps or uterine myomas. For this strategy, highly secure and safe cryopreservation protocols are advisable.
View Article and Find Full Text PDFJ Assist Reprod Genet
February 2012
IVF Centers Prof. Zech-Salzburg, Salzburg, Austria.
Background: To analyze the effects of embryo transfer (ET) quality on clinical pregnancy (CPR) and live birth delivery rates (LBDR).
Methods: In a retrospective study at a single, private infertility center between November 2005 and December 2009 one thousand fifty-five day-3 and day-5 ETs following IVF/ICSI/IMSI were evaluated. We analyzed the impact of an atraumatic ET with a soft catheter (ET 1), after external guidance (ET 2), after probing of the cervix with a stylet (ET 3), or after grasping the portio vaginalis with a tenaculum (ET 4) on CPR and LBDR.
Folia Biol (Praha)
May 2012
IVF Centers Prof. Zech - Pilsen s. r. o., Czech Republic.
Mouse embryonic carcinoma cells (P19 line) were studied for both their survival and developmental potential in the intact cerebellum of B6CBA mice. The P19 cells were cultured and labelled with green fluorescent protein using transfection. Cells were used for transplantation either in the undifferentiated stage or after 3 days of neurodifferentiation induced by retinoic acid.
View Article and Find Full Text PDFFertil Steril
June 2011
IVF Centers Prof. Zech, Bregenz, Austria.
Because of its size of 32 kDa and physicochemical properties, urinary FSH cannot permeate intact skin. We report the first pregnancy after laser microporation and transdermal delivery of FSH for ovarian superovulation as a substitute for SC or IM injections.
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