Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03323892
Other study ID # 2017/271
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date December 31, 2023

Study information

Verified date January 2023
Source Universitair Ziekenhuis Brussel
Contact Neelke De Munck, PhD
Phone 024776694
Email neelke.demunck@uzbrussel.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim the investigators study is to analyze the embryo development if oocytes of the participants are injected with sperm from a longer or shorter (2 hours) abstinence duration.


Description:

Participants undergoing an IVF treatment, are asked to respect an abstinence duration of 2-7 days. This is to obtain a sufficient number of motile sperm. A recent investigation, analyzed the quality (number and motility) of a sperm sample produced after an abstinence duration of 4 to 7 days, followed by a second sperm sample 2 hours later. The second sample (after 2 hours) was able to produce sperm cells with a higher motility. Not only has this short abstinence duration of 2 hours a positive effect on the motility, it will also reduce the sperm DNA damage, which again has a positive effect on embryo development. Because participants need gametes of high quality to obtain embryos with a high quality, the investigators want to investigate what the effect is of abstinence duration on embryo development.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 31, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients planned for embryo development up to day 5 - at least 6 mature oocytes - fresh ejaculates - ICSI - fresh embryo transfer or freeze all strategy - all stimulation protocols - concentration of >1x10^6 /ml sperm Exclusion Criteria: - IVF - IVF versus ICSI patients - chirurgical sperm - acceptors of donor oocytes - patients with PGD - patients already enrolled in another study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
second masturbation
Husbands will be asked to produce a second sperm sample in the masturbatorium

Locations

Country Name City State
Belgium Universitair Ziekenhuis Brussel Brussels

Sponsors (1)

Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Embryo development (blastocyst stage) embryo development 5/6 of the preimplantation development 1 year
Primary Embryo development (cleavage stage) embryo development on day 3 of the preimplantation development 1 year
Secondary Fertilization number of fertilized oocytes per number of mature oocytes 1 year
Secondary Utilization rate number of embryos used for transfer + cryopreserved for the patient 1 year
Secondary Sperm quality concentration and motility 1 year
Secondary Sperm DNA fragmentation analysis of non-viable sperm in the two samples 1 year
Secondary Clinical Pregnancies pregnancies with a fetal heart beat 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT03817671 - The Clinical Outcome of Ultra-low Oxygen Tension on Post Thawed Human Blastocyst N/A
Recruiting NCT02575924 - Influence of Culture Media on Clinical Outcomes in Poor Responders or Severe Male Infertility Phase 1
Completed NCT01767805 - Impact of Culture Conditions on the Embryo Quality N/A
Recruiting NCT02651285 - Use of G-CSF Supplemented IVF Medium in Patients Undergoing IVF Phase 4
Completed NCT01094314 - Impact of Culture Medium on Embryo Quality N/A
Completed NCT00718822 - Outcome of Embryo Culture at Two Oxygen Tensions N/A
Recruiting NCT03497052 - Culture Media and Blastocyst Development