Overview

Study to Examine Effect of Recombinant Luteinizing Hormone (r-Lh) and Recombinant Human Chorionic Gonadotropin (r-hCG) for Ovarian Stimulation in Assisted Reproduction Techniques (ART)

Status:
Completed
Trial end date:
2012-07-01
Target enrollment:
0
Participant gender:
Female
Summary
The study is a prospective, randomised, controlled, and non-blinded multi-center pilot study to evaluate endocrine efficacy of recombinant luteinizing hormone versus recombinant human chorionic gonadotropin administered during controlled ovarian stimulation for IVF/ICSI in normogonadotrophic women.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Regionshospitalet Viborg, Skive
Treatments:
Chorionic Gonadotropin
Follicle Stimulating Hormone
Hormones
Criteria
Inclusion Criteria:

- Women who plan to undergo IVF or ICSI treatment

- Woman's age > 18 years but ≤ 35 years

- Regular menstrual cycle (25-34 days)

- BMI 18 to 30 inclusive

- Signed patient information and informed consent forms

Exclusion Criteria:

- PCOS

- More than 2 prior IVF/ICSI attempts

- Diabetes mellitus, epilepsy, lever-, kidney-, heart- and metabolism disorders,
according to the Investigator's assessment.