Sperm Quality in Consecutive Sperm Samples After 4-7 Days and 2 Hours of Sexual Abstinence
NCT ID: NCT02667080
Last Updated: 2017-01-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
43 participants
INTERVENTIONAL
2014-04-30
2016-11-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Ejaculatory Abstinence on Semen Parameters in Male Factor Infertility Patients
NCT04206800
Abstinence Period and Semen Quality
NCT04955782
Second Ejaculate and IUI
NCT05173038
Assessing the Effect of Abstinence Period on Semen Parameters
NCT05701163
Ejaculation Abstinence Time and Assisted Reproductive Technology Outcomes
NCT06410417
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Ejaculate 1
Semen sample after 2-7 days of sexual abstinence
2-7 days of Sexual abstinence
2-7 days of Sexual abstinence
Ejaculate 2
Semen sample after 2 hours of sexual abstinence
2 hours of sexual abstinence
2 hours of sexual abstinence
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
2-7 days of Sexual abstinence
2-7 days of Sexual abstinence
2 hours of sexual abstinence
2 hours of sexual abstinence
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* able to understand and read Danish
Exclusion Criteria
* significant psychological illness
* significant cardiovascular disease
18 Years
50 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Aalborg University Hospital
OTHER
Aalborg University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hiva Alipour
Ph.D. Student, Research Assistant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Ole Bjarane M.D., Ph.D., M.D., Ph.D.
Role: STUDY_DIRECTOR
Aalborg University Hospital, Gynecology Department
Hiva Alipour, D.V.M.
Role: PRINCIPAL_INVESTIGATOR
Aalborg University, Faculty of Medicine, Department of Health Science and Technology
Fereshteh Dardmeh, D.V.M.
Role: STUDY_CHAIR
Aalborg University, Faculty of Medicine, Department of Health Science and Technology
Gerhard Van DerHorst, Ph.D.
Role: STUDY_CHAIR
University of the Western Cape, Capetown, South Africa
Christina Hnida, Ph.D.
Role: STUDY_CHAIR
Aalborg University Hospital, Gynecology Department
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Aalborg University Hospital, Dronninglund Fertility Clinic
Dronninglund, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
N-20140023
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.