Mesalamine and Reproductive Health Study (MARS)
The purpose of this study is to investigate the relationship of high exposure to dibutyl phthalate (DBP) from the use of Asacol with clinical and intermediate markers of male fertility, including semen quality, sperm DNA damage, transcript profiles of sperm mRNA and sncRNAs, and reproductive hormones.
Hypothesis 1: High exposure to DBP from the use of Asacol is associated with decreased sperm concentration and motility, and increased sperm DNA damage.
Hypothesis 2: High exposure to DBP from the use of Asacol is associated with decreased serum testosterone, altered LH:testosterone ratio, and decreased inhibin-B.
Hypothesis 3: High exposure to DBP from the use of Asacol is associated with altered transcript profiles of sperm mRNAs and sncRNAs.
|Study Design:||Observational Model: Case-Crossover
Time Perspective: Prospective
|Official Title:||Crossover Study on Human Exposure to Phthalates and Male Fertility|
- Altered semen quality and sperm transcriptome analysis [ Time Frame: Initial analysis takes place approximately 4-5 months after patient enrolls and after he has completed first crossover of medication. The second phase takes place about 8-10 months later after he crosses back to original medication. ] [ Designated as safety issue: No ]
- Serum levels of reproductive hormones [ Time Frame: Analysis of hormone levels take place at the same intervals decribed above, 4-5 months after enrollment and then again 8-10 months after enrollment when patient has resumed taking orginal medication. ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
Blood for hormones, urine for phthalates, semen for DNA and RNA
|Study Start Date:||May 2010|
|Estimated Study Completion Date:||February 2017|
|Estimated Primary Completion Date:||February 2016 (Final data collection date for primary outcome measure)|
men with inflammatory bowel disease
Men between the ages of 18-55 with inflammatory bowel disease who are taking mesalamine medication.
There are 2 ways you can participate in the study.
OPTION 1 involves 6 one-hour visits to the Massachusetts General Hospital (MGH) Andrology Clinic over a 9 month period. At each visit you would be asked to fill out questionnaires and to provide a urine, semen, and blood sample. Following Visit 2, you are asked to switch your brand of mesalamine medication. After 4 months, you change back to your original brand of medication. The change in medication will be done in consultation with your primary GI doctor. If the cost of co-payment is greater for the new brand of medication, we will provide compensation to cover the difference. In the case you do not have prescription drug health insurance coverage, the study will reimburse up to $4000 to cover the cost for Asacol, Pentasa or Lialda medication taken during your study participation.
OPTION 2 involves 4 one-hour visits to MGH Andrology clinic. At each visit you complete questionnaires and provide a blood, urine and semen sample. You are eligible for Option 2 if you are currently taking Asacol or Asacol HD and do not want to change your medication.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01331551
|Contact: Patricia R Morey, MEdfirstname.lastname@example.org|
|Contact: Jennifer Ford, BS, RNemail@example.com|
|United States, Massachusetts|
|Massachuetts General Hospital||Recruiting|
|Boston, Massachusetts, United States, 02114|
|Contact: Jennifer Ford, BS 617-643-2502 firstname.lastname@example.org|
|Contact: Myra Keller, RN 617-643-2502 email@example.com|
|Principal Investigator:||Russ B Hauser, MD, ScD, MPH||Harvard School of Public Health|