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Clinical Trials/NCT06179420
NCT06179420Not yet recruitingNot Applicable

The Effectiveness of Advanced Decision Support Tool (OPT-IVF) for IVF Treatment

National University of Malaysia1 site in 1 country30 target enrollmentStarted: March 13, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
total cumulative dosage of Gonadotropins

Study Overview

Brief Summary

This prospective study is subject to approval of institutional medical research ethics committee. Patient undergoing second cycle IVF will be enrolled into the intervention group. Intervention involved using a clinical decision support tool, Opt-IVF to guide gonadotrophins dosing and trigger dates for a personalized controlled ovarian stimulation cycle based on the distribution of follicle sizes on day 1 and day 5, and hormone dosages given on day 1 to 4.

Patients will undergo transvaginal ultrasound exam on day 1 and day 5 of the cycle to determine the number and size of follicles present. The data is used in the Opt-IVF decision support tool to suggest Gonadotropin dosage for D5 and beyond and to recommend the antagonist start day and trigger day.

Clinical investigators will not override the Opt-IVF recommended dosage in any patients.

Detailed Description

The total dosage of gonadotrophin, number of good quality oocytes and blastocyst will be analyzed from each arm.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patient undergoing 2nd cycle of IVF

Exclusion Criteria

  • Polycystic ovarian syndrome patient

Outcomes

Primary Outcomes

total cumulative dosage of Gonadotropins

Time Frame: for 1 year duration

number of total dosage that utilize during one cycle of IVF treatment

Total number of matured oocytes

Time Frame: for 1 year duration

number of matured oocytes following the stimulation protocol

total number of good quality blastocyst

Time Frame: for 1 year duration

total blastocyst achieved after each sti,ulation protocol

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
National University of Malaysia
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Azrai Abu

Associate Prof

National University of Malaysia

Study Sites (1)

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