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WithdrawnNCT02262923Updated Apr 11, 2022

Dopamine D-2 Antagonist Use in Poor Responders in IVF: a Randomized Controlled Trial

An interventional study of metoclopramide in in Vitro Fertilization and Poor Responder, sponsored by Mount Sinai Hospital, Canada. Withdrawn at 1 site in Canada. Open to female participants aged 21 Years to 43 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-11.

Sponsored by Mount Sinai Hospital, Canada · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
21 Years to 43 Years
Sex
Female
01

Study summary

Metoclopramide is a dopamine D2 receptor antagonist with antiemetic and gastrokinetic properties which has been approved for use in pregnant women. Women with polycystic ovary syndrome (PCOS) have been found to have lower dopaminergic tone and increased ovarian vascularity and vascular endothelial growth factor (VEGF) levels compared to controls. During ovarian stimulation, PCOS patients exhibit greater sensitivity to gonadotropins and increased follicular development. Administration of dopamine D2 antagonists may mimic the low dopaminergic tone noted in PCOS patients, increase VEGF levels, angiogenesis, and subsequently improve follicular growth during ovarian stimulation. This strategy could be used to improve IVF outcomes in poor responders.

The investigators hypothesize that, compared to gonadotropin use alone, the use of metoclopramide in combination with gonadotropins in poor responders undergoing IVF will result in an increased number of mature oocytes obtained at oocyte retrieval and improved IVF outcomes.

Read the detailed description

Poor responders constitute a significant and challenging population of women to treat with in vitro fertilization (IVF). This population includes women who respond sub-optimally to conventional ovarian stimulation with poor follicular recruitment. The estimated incidence of poor ovarian response ranges from 9-26%. Patients with PCOS are on the opposite end of the spectrum from poor responders. They are often exquisitely sensitive to ovarian stimulation and are predisposed to over-respond with the development of ovarian hyperstimulation syndrome (OHSS). Understanding the underlying mechanisms that enhance their sensitivity may provide insight into the treatment of poor responders. VEGF is a glycoprotein produced by ovarian granulosa cells that enhances vascular permeability and angiogenesis, and has been implicated in the pathogenesis of OHSS. After ovulation is triggered by LH or hCG, follicular expression of VEGF increases, which is crucial for corpus luteum function and steroidogenesis. However, excessive VEGF production can lead to third-space shifts of fluids, ascites, and other life-threatening features of OHSS. Serum concentrations and granulosa cell expression of VEGF have been shown to be higher in women with PCOS than in controls. Interestingly, compared with controls, patients with PCOS have also been shown to have lower levels of the neurotransmitter dopamine and dopamine D2 receptor levels in the ovary. Administration of dopamine D2 agonists has been shown in animal and human studies to decrease ovarian VEGF production and reduce the risk of OHSS. In this study, the investigators propose a novel approach of administering a dopamine D2 antagonist to poor responders to mimic the low dopaminergic tone of PCOS patients, with the goal of increasing VEGF production and follicular development during ovarian stimulation. Metoclopramide is a dopamine D2 antagonist with antiemetic and prokinetic properties and an established safety profile in pregnancy. The investigators hypothesis is that metoclopramide use prior to, and in conjunction with, conventional gonadotropin stimulation can improve IVF outcomes in poor responders.

02

Conditions studied

  • in Vitro Fertilization
  • Poor Responder
03

In context

Lead sponsor

Mount Sinai Hospital, Canada is the lead sponsor of 157 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 43 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Poor responders undergoing a repeat IVF cycle defined as women who have undergone at least one previous IVF cycle with fewer than 4 oocytes retrieved and at least one of the following:

    • Advanced age (≥40 years) or any other risk factor for poor ovarian response
    • Abnormal ovarian reserve testing (antral follicle count (AFC) \< 5-7 or anti-mullerian hormone (AMH) level \< 3.6-7.9 pmol/L)

Exclusion criteria

Exclusion Criteria:

  • Subjects who have previously been recruited into this study and either had cycle cancellation, underwent retrieval or dropped out of the study.
  • Women with contraindications or allergies to metoclopramide.
  • Women with elevated prolactin levels or known to have pituitary microadenomas or macroadenoma.
  • Women who are taking dopamine agonist medications.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
0 participants (actual)

Study arms

  • No intervention
    Control

    Poor responders will be defined as women who have undergone a previous IVF cycle with fewer than 4 oocytes retrieved and at least one of the following two criteria: (1) advanced age (≥40 years) or any other risk factor for poor ovarian response and (2) abnormal ovarian reserve testing (antral follicle count (AFC) \< 5-7 or anti-mullerian hormone (AMH) level \< 3.6-7.9 pmol/L). Poor responders who will be undergoing a repeat IVF cycle will be recruited for the study with informed consent. In the control arm, patients will undergo the same ovarian stimulation protocol as the previous IVF cycle in which they experienced a poor response. Starting 3 weeks prior to the first day of stimulation until the time of ovulation trigger (approximately 5 weeks overall), these patients will receive an oral placebo three times daily.

  • Experimental
    Experimental

    Poor responders will be defined as women who have undergone a previous IVF cycle with fewer than 4 oocytes retrieved and at least one of the following two criteria: (1) advanced age (≥40 years) or any other risk factor for poor ovarian response and (2) abnormal ovarian reserve testing (antral follicle count (AFC) \< 5-7 or anti-mullerian hormone (AMH) level \< 3.6-7.9 pmol/L). Poor responders who will be undergoing a repeat IVF cycle will be recruited for the study with informed consent. In the experimental arm, patients will undergo the same ovarian stimulation protocol as the previous IVF cycle in which they experienced a poor response. Starting 3 weeks prior to the first day of stimulation until the time of ovulation trigger (approximately 5 weeks in total), these patients will receive oral metoclopramide 5mg three times daily..

    Drug: metoclopramide

Interventions

  • Drugmetoclopramide
06

What researchers measure

Primary outcomes

  1. Number of oocytes retrieved

    Time frame: 1 year

Secondary outcomes

  1. Number of mature follicles (≥1.5cm) seen on transvaginal ultrasound at the time of ovulation trigger

    Time frame: 1 year

  2. Peak serum estradiol levels measured at the time of ovulation trigger shot

    Time frame: 1 year

  3. Ratio of mature/ immature oocytes obtained at oocyte retrieval

    Time frame: 1 year

  4. Follicular fluid levels of VEGF, VEGFR-1 and VEGFR-2

    Time frame: 1 year

  5. Total dose of gonadotropins used and number of days of stimulation

    Time frame: 1 year

  6. Fertilization rates

    Time frame: 1 year

  7. Number of embryos on day 3 and 5

    Time frame: 1 year

  8. Pregnancy and implantation rates

    Time frame: 1-2 years

  9. Serum prolactin levels on cycle day 3,7 and at the time of ovulation trigger

    Time frame: 1 year

07

Study locations

1 site
  • Mount Sinai Hospital
    Toronto, Ontario M5T 3H7, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02262923
Lead sponsor
Mount Sinai Hospital, Canada
Responsible party
Sponsor
First posted
Oct 13, 2014
Start date
Mar 2016
Primary completion
Mar 2018
Completion
Mar 2018
Last update
Apr 11, 2022

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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