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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02998593
Other study ID # Royan-Emb-026
Secondary ID
Status Recruiting
Phase Phase 3
First received November 9, 2016
Last updated April 26, 2017
Start date July 2016
Est. completion date June 2017

Study information

Verified date October 2016
Source Royan Institute
Contact Nasser Aghdami, MD,PhD
Phone (+98)23562000
Email nasser.aghdami@royaninstitute.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a prospective double blind randomized controlled trial to investigate the effect of red and white bahman on semen parameters, sexual hormones and DNA defragmentation in idiopathic oligospermic men .Include patients will take the medicine and placebo in different two case and control groups for 3 month and semen parameters and other variants at the start and end of study.


Description:

This is a randomized, double blind; placebo-controlled clinical trial has been started from july 2016 and will continue to july 2016 in Royan institute. The eligible patients who fulfilled the study criteria will be included in the trial.

Study protocol and assays All the patients will have a complete history evaluation and physical examination by the attending urologist who is blinded to the study and enter the study according to inclusion criteria.. semen analysis and hormonal laboratory tests [Testosterone, Luteinizing hormone (LH) Follicle stimulating hormone(FSH)] will done in same lab at start of study and 3 month after. Intervention time is 3 month for each patient. semen analysis wil be done according to who laboratory manual for the examination and processing of human semen 5th edition and hormonal tests (LH,FSH,Testosterone) with Elisa method (with score of International Unit). DNA Defragmentation will evaluate with Sperm Chromatin Structure Assay(SCSA) method. semen parameters which will evaluate is the number of normal and abnormal shape sperms, velocity of sperms, volume and viscosity of semen at start and end of the study. medicine and placebo prescribe in 500mg capsules for 3month. red and white Bahman is an effective medicine in male infertility treatment In Iranian Traditional Medicine. at the end of study main aim of the study is evaluation effect of combination of Red and White Bahman retrieved of Iranian Traditional Medicine on Semen Parameters in Idiopathic Oligospermic . Red Bahman and White bahman ,nutrition ,placebo, smoking and Testosterone,LH,FSH,Concentration,number,sha-pe,of sperm before and after the study is variables of study.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date June 2017
Est. primary completion date April 2017
Accepts healthy volunteers No
Gender Male
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

1. all idiopathic oligospermic patient in range of 20 to 45 years old

2. sperm count under 15 million /ml 3;No history of taking chemical or herbal medicine effective on sperm genesis in last 3 month( like Hormonal drug ,antidepressant ,anti hypertension,cimetidine, cyproteron, sulphasalazine, flutamide, spironolactone, estrogen,opium 4:No history of Varicocele and Obstructive disease 5:;No leukocytospermia

Exclusion Criteria:

Taking chemical or herbal medicine effective on spermatogenesis (hormonal and sperm reducing and increasing agent); 2. ; Increasing BMI > 30 3. Leukocytospermia 4. varicocele

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Bahman capsules
Oral Use of Bahman capsules for 3 months by patients.
Placebo
Oral use of placebo capsules by patients for 3 months.

Locations

Country Name City State
Iran, Islamic Republic of Royan Institute Tehran

Sponsors (1)

Lead Sponsor Collaborator
Royan Institute

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Semen analysis Performing the semen analysis to evaluate the sperm count ,sperm motility and sperm morphology. 3 months
Secondary Testosterone Evaluation the testosterone by ELISA level 3 months after intervention. 3 months
Secondary FSH Evaluation the FSH level by ELISA 3 months after intervention. 3 months
Secondary LH Evaluation the LH level by ELISA 3 months after intervention. 3 months
Secondary DNA defragmentation Evaluation the DNA defragmentation by SCSA Method 3 months after intervention. 3 months
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