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The Comparison of Effect of Four Different Treatment Protocols on IVF Outcomes in Poor Responders Undergoing in Vitro Fertilization.

P

Pınar Özcan Cenksoy

Status and phase

Unknown
Phase 4

Conditions

Poor Responders Undergoing IVF

Treatments

Drug: microdose flare-up protocol (Lucrin; Abbott + Gonal F, Serono)
Drug: Antagonist/clomiphene protocol (Cetrotide; serono + Klomen, Kocak pharma)
Drug: GnRH antagonist protocol (Cetrotide, Serono)
Drug: GnrH Antagonist/letrozole protocol (Cetrotide; serono + Femara; Novartis Pharma AG)

Study type

Interventional

Funder types

Other

Identifiers

NCT01948804
ytu-123 (Other Identifier)

Details and patient eligibility

About

The comparison of effect of four different treatment protocols: Antagonist/letrozole protocol, microdose flare-up protocol, Antagonist/clomiphene protocol, Antagonist on IVF outcomes in poor responders undergoing in vitro fertilization; a prospective randomized-controlled study.

Enrollment

100 estimated patients

Sex

Female

Ages

18 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Criteria for definition of poor responders included at least one of the following

  1. Anti müllerian hormone <1.1 ng/ml and/or a previous poor ovarian response (≤3 oocytes with a conventional stimulation protocol).
  2. Primary infertile patients
  3. BMI≤30 kg/m2 were included this study.

Exclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 1 patient group

IVF patients
Experimental group
Description:
patients that has applied to Yeditepe University Hospital assisted reproduction center
Treatment:
Drug: Antagonist/clomiphene protocol (Cetrotide; serono + Klomen, Kocak pharma)
Drug: microdose flare-up protocol (Lucrin; Abbott + Gonal F, Serono)
Drug: GnRH antagonist protocol (Cetrotide, Serono)
Drug: GnrH Antagonist/letrozole protocol (Cetrotide; serono + Femara; Novartis Pharma AG)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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