Trial intelligence / Profile preview

Flexible vs fixed progestin-primed ovarian stimulation in Poseidon group 1 and 2

TCTR20250316002Phase 3

Key facts

Status
Recruiting
Start
Feb 2025
Countries
1
Sponsor
Faculty of Medicine Research Fund
Modality
Small Molecules
Conditions
female infertility
01

Overview

Phase 3, randomised trial of hydroxyprogesterone caproate in female infertility (2 arms), sponsored by Faculty of Medicine Research Fund. Primary endpoint: Premature luteinizing hormone surge incidence. Started Feb 2025; status: recruiting.

02

Design

2 arms
Study design
Randomized
  • Flexible PPOS

    Flexible progestin-primed ovarian stimulation protocol with individualized timing of progestin initiation.

  • Fixed PPOS

    Fixed progestin-primed ovarian stimulation protocol with progestin initiation on a predetermined cycle day.

03

Who it enrols

Women in Poseidon group 1 or 2 with low prognosis undergoing assisted reproductive treatment and eligible for progestin-primed ovarian stimulation.

04

Endpoints

Primary

  • Premature luteinizing hormone surge incidence

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