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A study to compare 2 medical interventions in patients with low egg count to improve outcome of test tube baby treatment

Not Applicable
Conditions
Health Condition 1: N978- Female infertility of other origin
Registration Number
CTRI/2023/06/053760
Lead Sponsor
Oasis centre for Reproductive Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.All poor responders as defined by Poseidon criteria undergoing COS for IVF using antagonist protocol ( AFC less than or equal to 5 , AMH less than or equal to 1.2 ng/dl , unexpected poor response in previous cycle with oocytes retrieved less than or equal to 9)

2.Presence of both ovaries

Exclusion Criteria

1. Any current or past diseases affecting ovaries or gonadotrophin or sex steroid secretion, clearance or excretion

2. Hypogonadotrophic hypogonadism

3. Premature ovarian insufficiency ( FSH > 20 or no AFCs )

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
-Total days of stimulation <br/ ><br>-Total dosage of FSH used <br/ ><br>-Number of oocytes retrieved <br/ ><br>-FSH to Oocyte ratio <br/ ><br>-Follicle to oocyte index <br/ ><br>-Follicular output rate <br/ ><br>-M-II rate <br/ ><br>Timepoint: 1 month
Secondary Outcome Measures
NameTimeMethod
-Fertilisation rate <br/ ><br>-Cleavage rate <br/ ><br>-Blastulation rate <br/ ><br>-Cycle cancellation rate <br/ ><br>-Embryo utilisation rate <br/ ><br>-Implantation rate <br/ ><br>-Biochemical pregnancy rate <br/ ><br>-Clinical pregnancy rate <br/ ><br>-Miscarriage rate <br/ ><br>-Ongoing pregnancy rate <br/ ><br>-Live birth rate <br/ ><br>Timepoint: 1 year
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