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Effect of Metoclopramide on fertility in women with loss of ovarian reserve

Evaluation of the effect of dopamine D2 antagonist on the success of invitro fertilization in poor responders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015082622206N2
Enrollment
50
Registered
2016-06-19
Start date
2015-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

patients with poor ovarian response. Certain conditions originating in the perinatal period

Interventions

Intervention 1: Interventional group: Metoclopramide 10 mg 4 times/day (pre prandial and at the bed side) The drug started 4 weeks before starting IVF cycle and continued till triggering with HCG. Int
Treatment - Drugs
Placebo
Interventional group: Metoclopramide 10 mg 4 times/day (pre prandial and at the bed side) The drug started 4 weeks before starting IVF cycle and continued till triggering with HCG.
Control group: similar placebo effect drugs with the same dose. (pre prandial and at the bed side) The drug started 4 weeks before starting IVF cycle and continued till triggering with HCG.

Sponsors

Vice Chancellor for Medical Sciences Research of Shiraz University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: previous treatment using conventional protocols that yield less than 3 oocytes, abnormal ovarian reserve tests as AMH<0.5-1. 1ng/ml or AFC <5-7 Follicles, age over 40 years or any other risk factor that decrease the ovarian reserve such as previous ovarian surgery, genetic problems, chemotherapy, radiotherapy and autoimmune disease, having 2 or more of above factors (Bologna criteria). Exclusion criteria: not have above factors, no agreement of patient, she can not complete the coarse of treatment, become OHSS. (ovarian hyperstimulation syndrom)

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Clinical pregnancy or spontanous abortion. Timepoint: 7-12 weeks after embryo transfering. Method of measurement: Serum BHCG and TVS.

Primary

MeasureTime frame
Quality and number of ovum and embryo have received in each IVF cycle. Timepoint: On day of ovum pick up and embryo transfer. Method of measurement: Measuring number and quality of oocyte on the day of pick up in lab by embryologist under microscope (GV,MI,MII) and quality of embryo also by the same embryologist according to kind of cell division (grade I,II,III,IV).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Pardis Bakhshaeie

Shiraz Unicversity of Medical Sciences

Pardis.bakhshaie287@gmail.com+98 912 363 0119

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026