Is a Carnitine Based Food Supplement (PorimoreTM) for Infertile Men Superior to Folate and Zinc With Regard to Pregnancy Rates in Intrauterine Insemination Cycles?
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ClinicalTrials.gov Identifier: NCT01075334 |
Recruitment Status : Unknown
Verified February 2010 by Shaare Zedek Medical Center.
Recruitment status was: Recruiting
First Posted : February 25, 2010
Last Update Posted : February 25, 2010
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Condition or disease | Intervention/treatment | Phase |
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Male Infertility | Dietary Supplement: Porimore - A Carnitine based food supplement Dietary Supplement: Zinc and Folate Supplementation | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 100 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Study Start Date : | February 2010 |
Actual Primary Completion Date : | February 2010 |
Estimated Study Completion Date : | December 2012 |

Arm | Intervention/treatment |
---|---|
Experimental: Porimore arm
Infertile men will receive 'Porimore' tablets for a period of time in which three intrauterine insemination cycles will be performed.
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Dietary Supplement: Porimore - A Carnitine based food supplement
A daily dose of 2 grams L-carnitine, 1 gr acetyl L-carnitine, 500mg Vitamin C, 400 IU vitamin E, 60 mg Q10, 30mg Zinc Picolinate, 500mcg Folic Acid, 200 Mcg Selenium, 100 MCG Vitamin B12. |
Active Comparator: Folate and Zinc |
Dietary Supplement: Zinc and Folate Supplementation
500 Mcg Folic acid, 30-60 mg Zinc tablets/ day |
- Pregnancy Rate [ Time Frame: 3 Insemination cycles ]proportion of women becoming pregnancy following treatment with intrauterine insemination
- Sperm quality parameters [ Time Frame: 3 months ]

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Ages Eligible for Study: | 18 Years to 50 Years (Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- infertility
- at least one abnormal sperm quality parameter
- female age < 35
- normal ovarian reserve
Exclusion Criteria:
- known allergy to one of the food additives planned for treatment

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01075334
Contact: Avi Tsafrir, MD | 972-6555111 | avits@szmc.org.il |
Israel | |
Shaare-Zedek IVF and infertility unit | Recruiting |
Jerusalem, Israel, 91031 | |
Principal Investigator: Avi Tsafrir, MD |
Responsible Party: | Avi Tsafrir, MD, IVF Unit, Shaare Zedek Medical Center, Jerusalem, Israel |
ClinicalTrials.gov Identifier: | NCT01075334 |
Other Study ID Numbers: |
porimore.CTIL |
First Posted: | February 25, 2010 Key Record Dates |
Last Update Posted: | February 25, 2010 |
Last Verified: | February 2010 |
sperm male infertility Carnitine food supplementation insemination |
Infertility Infertility, Male |