ClinicalTrials.gov record
Completed Not applicable Interventional Accepts healthy volunteers

Mono-menotropins Versus rFSH Protocol on Embryo Quality

ClinicalTrials.gov ID: NCT02418533

Public ClinicalTrials.gov record NCT02418533. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 8:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Randomized Trial to Compare Mono-menotropins Protocol for Controlled Ovarian Stimulation (COS) Versus Recombinant Follicle Stimulating Hormone (rFSH) Protocol on Embryo Quality Parameters in IVF Patients

Study identification

NCT ID
NCT02418533
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Main Line Fertility Center
Other
Enrollment
109 participants

Conditions and interventions

Interventions

  • Recominant Follicle Stimulating Hormone (rFSH) Drug
  • menotropin Drug

Drug

Eligibility (public fields only)

Age range
21 Years to 38 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2015
Primary completion
Mar 31, 2017
Completion
Jun 30, 2017
Last update posted
Aug 11, 2020

2015 – 2017

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Main Line Fertility Center Bryn Mawr Pennsylvania 19010

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02418533, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 11, 2020 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02418533 live on ClinicalTrials.gov.

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