The Fertility Clinic, Regional Hospital of Skive
Skive, 7800, Denmark
NCT Number: NCT00627406
The purpose of this study is to possibly further improve the clinical outcome and explore the incidence of OHSS in patients, who have final oocyte maturation with GnRHa (Buserelin) in GnRH antagonist IVF/ICSI cycles
Looking for future studies?
Notify Me20 year–39 year
Female
Interventional
Phase 4
Skive, 7800, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subcutaneous injection 0.5 mg and 1500 IU
Subcutaneous injection 5000 IU
Time frame: From the date of triggering ovulation until 2 weeks after pregnancy test. group C and D. 12 days after pregnancy test
Time frame: from stimulation day 1 until last ultrasound scan 7 weeks after a positive pregnancy test
Regionshospitalet Viborg, Skive
Other
A Prospective Randomised Study to Evaluate the Effect of Triggering Ovulation With GnRHa (Buserelin) and Low Dose hCG (Pregnyl) as Compared to the Use of Conventional Doses of hCG (Pregnyl)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06333691
Adnexal Diseases, Endocrine System Diseases
Minya, Egypt
View Trial DetailsNCT05362734
Adnexal Diseases, Endocrine System Diseases
View Trial DetailsNCT05588635
Adnexal Diseases, Endocrine System Diseases
Metz, France
View Trial DetailsNCT03876145
Adnexal Diseases, Cysts
Tehran, Iran
View Trial Details