Pregnancy and Childbirth: In vitro fertilisation (IVF) Pregnancy and Childbirth Procreative management
Conditions
Interventions
Randomised controlled trial, Random allocation to receive HCG injection at:
1. Standard time delay
2. 24 h delay
3. 48 h delay
Sponsors
Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Patients undergoing their first or second cycle of IVF or IVF/intracytoplasmic sperm injection (ICSI). 2. Age of partner 19-36 years. 3. Body mass index 20-30 kg/m2. 4. Serum follicle-stimulating hormone (FSH) concentration in normal range.
Exclusion criteria
Exclusion criteria: Does not match inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main objective is to determine whether there is an optimal time to give HCG injection, and also to observe any differences in the number of eggs being collected, fertilisation rates, embryos quality and pregnancy rates among the three groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed