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Effect of Taroneh on treatment of male infertillity

Phase 3
Conditions
male infertility.
Male infertility
Registration Number
IRCT2014111519965N1
Lead Sponsor
Vice chancellor for research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
80
Inclusion Criteria

Inclusion Criteria: Idiopathic oligospermia; Idiopathic Asthenospermia; Idiopathic Teratospermia; Idiopathic Oligoasthenospermia; Idiopathic Oligoteratospermia; Idiopathic Oligoteratoasthenospermia; 18-35 Age; Patient’s wife age 18-35; Absence of azoospermia; Non-consuming use of other drug for
treatment of infertility during the study
Exclusion criteria: lack of patient cooperation; the incidence of
serious side effects, Age more than 35, Age of patient’s spouse more than 35

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sperm count concentration. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.;Total sperm count. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.;Motility. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.;Morphology. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.
Secondary Outcome Measures
NameTimeMethod
pper respiratory tract's reaction to Taroneh. Timepoint: When the incidence of adverse drug reactions in patient. Method of measurement: According CTC (Common Toxicity Criteria).;Volume. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.;Viscosity. Timepoint: Before intervention and then four months after the start of intervention (one month after the end of intervention). Method of measurement: Semen analysis.
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