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Efficacy of Metoclopramide in Poor Ovarian Response IVF Patients

Efficacy of Metoclopramide in Poor Ovarian Response IVF Patients: a Randomised, Double-blind, Placebo-controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03560583
Enrollment
60
Registered
2018-06-18
Start date
2021-05-05
Completion date
2028-07-31
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Poor Responders in IVF

Brief summary

Poor ovarian response population of ART are considered the biggest challenge for providers. Hitherto, no one protocol has been proven to be effect in this subgroup of IVF patients. Metoclopramide belongs to the antiemetic group, used for motion sickness and during early gestation for hyperemesis gravidarum. The mechanism of action is antagonisim to dopamine receptors. We hypothesize than by blocking dopamine receptors and decreasing the dopaminergic tone there is a possibility to increase the sensitivity of ovarian response to gonadotropins during controlled ovarian stimulation and result in increased oocyte retrival.

Interventions

DRUGMetoclopramide

Metoclopramide 10 mg BID

DRUGPlacebo Oral Tablet

Placebo 10 mg BID

Sponsors

Barzilai Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 54 Years
Healthy volunteers
Yes

Inclusion criteria

* Poor response according to Bologna criteria

Exclusion criteria

* Allergy to metoclopramide * Prolactinemia * Women treated with dopamine agonists

Design outcomes

Primary

MeasureTime frameDescription
Number of oocytesApproximately 5 weeks from first dose of study drugNumber of oocytes

Countries

Israel

Contacts

Primary ContactLeon Grin, MD
leonti.grin@gmail.com972-50-5999379

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026