Status:

COMPLETED

Cabergoline Before or After Oocyte Collection for Follicular Resolution

Lead Sponsor:

Fertility Center of Las Vegas

Conditions:

Infertility, Female

Eligibility:

FEMALE

18+ years

Phase:

PHASE4

Brief Summary

Randomized trial comparing the efficacy of two different times of administration of cabergoline in patients undergoing controlled ovarian stimulation and oocyte collection.

Eligibility Criteria

Inclusion

  • Adult female at least 18 years of age intending to undergo ovarian stimulation for a cycle of IVF.
  • Ability read and understand English sufficiently to obtain informed consent and complete a study diary.
  • Pre-implantation genetic screening (PGS) is allowed.
  • Egg donors are allowed.
  • Patients using a gestational carrier are allowed.
  • Patients with prior IVF cycles are allowed, but no patient can undergo more than one cycle with oocyte collection under this study.

Exclusion

  • Egg banking, donor egg banking, or any cycle type that would preclude immediate culture to blastocyst stage.
  • Patients that would be unavailable for the follow-up ultrasound 5 days post-retrieval, such as patients that live far from the clinic (e.g. out of state).
  • Uncontrolled hypertension.
  • Ergot alkaloid hypersensitivity or allergy.
  • History of pulmonary, pericardial, retroperitoneal fibrotic disorders.
  • History of bipolar disorder, schizophrenia, or psychotic illness.
  • Breast feeding.
  • History of eclampsia or pre-eclampsia.
  • Severe hepatic dysfunction.
  • Current use of any dopamine receptor agonist or antagonist for any purpose, including, but not limited to, cabergoline (Dostinex), aripiprazole (Abilify), bromocriptine (Parlodel), methylphenidate (Ritalin), buproprion (Wellbutrin, Zyban), lisdexamfetamine (Vyvanse).
  • Any condition that, in the opinion of the physician or principal investigator, would place the patient at undue risk under this protocol or would otherwise make the protocol inappropriate for that subject.

Key Trial Info

Start Date :

September 23 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 10 2021

Estimated Enrollment :

70 Patients enrolled

Trial Details

Trial ID

NCT04096027

Start Date

September 23 2019

End Date

June 10 2021

Last Update

June 14 2021

Active Locations (1)

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Fertility Center of Las vegas

Las Vegas, Nevada, United States, 89117