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Investigating the effect of pyridostigmine in individuals with poor ovarian response

Phase 3
Recruiting
Conditions
Infertility.
Female infertility
Registration Number
IRCT20100518003950N8
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
110
Inclusion Criteria

Women with a history of poor response to ovarian stimulation in previous cycles who are willing to undergo a new cycle.

Exclusion Criteria

BMI more than 30
Respiratory diseases (such as asthma, COPD), renal disease, slow or irregular heartbeat, a history of slow bowel movements and constipation (due to the possibility of delayed drug metabolism), or metabolic disorders.
Taking any other cholinergic drug.
Endometriosis, stage III-IV
History of allergic reactions
Taking psychotropic medications and corticosteroids

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Retrieved Oocytes. Timepoint: 36 hours after receiving the ovulation induction. Method of measurement: Laboratory count.
Secondary Outcome Measures
NameTimeMethod
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