Trial Profile

A Multicenter, Randomized, Controlled, Double-blind, Double-dummy Study to Evaluate the Safety and Efficacy of Subcutaneous Progesterone Compared to Vaginal Progesterone for Luteal Phase Supplementation in Modified Natural Frozen Euploid Blastocyst Transfer.

Status: Recruiting

Phase of Trial: Phase III

Latest Information Update: 09 Apr 2025

Price :

$35 ^*

Note:

Adis is an information provider.
Final gross price and currency may vary according to local VAT and billing address.
Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

Drugs Progesterone (Primary) ; Progesterone (Primary) ; Progesterone (Primary) ; Progesterone (Primary)
Indications Female infertility
Focus Registrational; Therapeutic Use
Acronyms PROGRESS
Sponsors IBSA

03 Apr 2025 Planned End Date changed from 30 Apr 2026 to 30 Jun 2026.
03 Apr 2025 Planned primary completion date changed from 31 Aug 2025 to 30 Dec 2025.
19 Sep 2024 Planned End Date changed from 1 Mar 2025 to 30 Apr 2026.

If your organization or you do not have a subscription, try one of the following:

Contacting your organization’s admin about adding this content to your AdisInsight subscription
Buying a PDF version of any individual profile
Request a free trial (opens in a new window)

If your organization has a subscription, there are several access options, even while working remotely:

Working within your organization’s network
Login with username/password or try to access via your institution
Persisted access using your organization’s identifier stored in your user browser for 90 days

For assistance, contact us at asktheexpert.adisinsight@springer.com