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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05885516
Other study ID # B.10.1.TKH.4.34.H.GP.0.01/384
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 5, 2023
Est. completion date December 22, 2024

Study information

Verified date November 2023
Source Umraniye Education and Research Hospital
Contact Merve Dizdar, Speacialist
Phone +905355962232
Email mervedizdar@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to compare the pregnancy outcomes of single vs double intrauterine insemination (IUI) in couples with male factor infertility.


Description:

The principle behind double intrauterine insemination in male factor infertility couples is to create a longer time frame for fertilization and to increase motile sperm number in female genital tract in order to increase pregnancy rates. There's a clinical equipoise on the benefits of performing double IUI in couples following ovarian hyperstimulation with daily follicle stimulating hormone injections in male factor subfertility. As it is stated in Cochrane database, there's a need for adequately powered, randomized, high-quality studies on this subject. In this study, as a result of a-priori power analysis 132 participants in each study arm is planned to be recruited in the study. Male factor infertility included in the study is defined as total motile sperm count (TPMSC) less than 10 million. TPMSC less than 1 million, female age greater than 40, uterine anomaly, no patent tubes shown in hysterosalpingography, history of ovarian surgery and known endometriosis will be excluded. Couples with two basal semen analysis with TPMSC between 1-10 million will be randomized to single or double IUI procedure. To accomplish this in approximately 1 year period, the study is planned as a multi-center study. The objective of the study is to compare the pregnancy outcomes of single and double intrauterine insemination groups, following ovarian hyperstimulation in couples with male factor subfertility.


Recruitment information / eligibility

Status Recruiting
Enrollment 264
Est. completion date December 22, 2024
Est. primary completion date November 22, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Couples trying to conceive for at least 6 months despite of regular sexual intercourse - Female partner between 18-40 years old - Male partner sperm analysis total motile sperm count between 1-10 million in at least 2 sperm analysis on different days. Exclusion Criteria: - No patent fallopian tubes shown in hystero-salpingography - Female partner with a uterine anomaly - History of a previous ovarian surgery - Known or suspected endometriosis in female partner - Body-mass index (BMI) > 40 kg/m2

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
intrauterine insemination
Giving washed sperm concentrate into uterine cavity via a soft catheter

Locations

Country Name City State
Turkey Umraniye Training and Research Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Umraniye Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Bagis T, Haydardedeoglu B, Kilicdag EB, Cok T, Simsek E, Parlakgumus AH. Single versus double intrauterine insemination in multi-follicular ovarian hyperstimulation cycles: a randomized trial. Hum Reprod. 2010 Jul;25(7):1684-90. doi: 10.1093/humrep/deq112. Epub 2010 May 10. — View Citation

Rakic L, Kostova E, Cohlen BJ, Cantineau AE. Double versus single intrauterine insemination (IUI) in stimulated cycles for subfertile couples. Cochrane Database Syst Rev. 2021 Jul 14;7(7):CD003854. doi: 10.1002/14651858.CD003854.pub2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of clinical pregnancy Pregnancy with fetal cardiac activity diagnosed by transvaginal ultrasonography Within 4-6 weeks after insemination
Secondary Rate of biochemical, ectopic pregnancies and rate of miscarriages Pregnancy outcomes including biochemical, ectopic pregnancies and miscarriages diagnosed by transvaginal ultrasonography Within 3 months after insemination
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03978013 - Pomegranate Juice Effect on Oxidative Stress in Infertile Women During IVF Treatment N/A
Completed NCT01661010 - The Clinical Study of Sex Chromosome Variants
Recruiting NCT02992665 - Can Calcium Ionophore Application Enhance the ICSI Outcomes in Severe Male Factor Infertility? Phase 2/Phase 3
Completed NCT00741494 - Effectiveness of the Use of the PICSI Dish (Hyaluronan Microdot) in the Selection of Sperm for Intracytoplasmic Sperm Injection (ICSI) N/A