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Infertility clinical trials

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NCT ID: NCT04591470 Completed - Clinical trials for Male Infertility Due to Antisperm Antibody

Influence of Inguinal Hernia Repair on Sperm Autoimmunity

SPERMAR
Start date: June 1, 2020
Phase:
Study type: Observational

Influence of inguinal hernia repair on sperm autoimmunity using MAR test

NCT ID: NCT04572659 Completed - Anxiety Depression Clinical Trials

Psychosocial Intervention in Assisted Reproduction Treatments

Start date: March 25, 2015
Phase: N/A
Study type: Interventional

The aim of the study was to evaluate and compare different strategies of psychosocial intervention for patients undergoing IVF treatment in a private fertility clinic. Recruited patients were assigned to one of three groups: group intervention, couple intervention or no intervention (control group). Three main variables were assessed: depression, anxiety and life quality.

NCT ID: NCT04537078 Completed - Infertility, Female Clinical Trials

Progestin Primed Double Stimulation Protocol Versus Flexible GnRH Antagonist Protocol in Poor Responders

Start date: September 1, 2020
Phase: Phase 3
Study type: Interventional

The worldwide prevalence of primary and secondary infertility is estimated at ~2% and 10.5%, respectively, among women aged 20-44 years and attempting to conceive. Poor ovarian responders (PORs) involve 9-24% of patients undergoing in-vitro fertilization (IVF). proper tailoring of the ovarian stimulation protocol in order to maximize the number of oocytes collected represents a crucial step for them to eventually conceive. Recent evidence indicates that in the same menstrual cycle, there are multiple follicular recruitment waves. This coincides with the theory that folliculogenesis occurs in a wave-like fashion. Thus, within a single menstrual cycle, there can theoretically be multiple opportunities for a clinician to collect oocytes, as opposed to the conventional single cohort of antral follicles during the follicular phase. Utilizing this concept, clinicians have been attempting to retrieve oocytes from poor responders using both the follicular-phase stimulation (FPS) and the luteal-phase stimulation (LPS) protocols to increase the number of oocytes collected shorter within shorter period of time. By increasing the number of the retrieved oocytes collected, a better clinical can be assured since there is a clear relationship between the number of oocytes collected and live birth rates across all female age groups. which protocol is the most effective remains controversial and the efficacy of PPOS in POR compared with that of conventional protocols is unclear.

NCT ID: NCT04536545 Completed - Clinical trials for Sperm Parameters in Fertile and Infertile Men

Evaluation of New Semen Collection & Transportation Kit

Start date: August 31, 2020
Phase:
Study type: Observational

Examine the effect of overnight transport conditions on sperm parameters on semen samples collected and mailed to Cleveland Clinic Andrology center.

NCT ID: NCT04509869 Completed - Pain Clinical Trials

"Outcome of Varicocelectomy on Normal Semen in Patients Complaining of Orchialgia

Start date: August 12, 2017
Phase: N/A
Study type: Interventional

varicoclelectomy is done for subfertiltiy and varicocele induced orchialgia. The effect of varicocelectomy on semen analysis is controversial. Many articles report favorable outcomes and others do not. Most study don't focus on varicocelectomy done for varicocele induced orchialgia,and those studies dont report on postoperative semen. This study will focus on the effect of operation on the semen postoperatively .

NCT ID: NCT04509583 Completed - Infertility, Male Clinical Trials

The Role of Micro Nutrient Supplement in Improvement of the Sperm DNA Fragmentation

Start date: November 18, 2019
Phase: N/A
Study type: Interventional

Male from infertile couples are tested for semen analysis and sperm DNA fragmentation. Any case with high DNA fragmentation index (DFI) will be randomized indicated for multi-micro nutrient supplement (PROfortil™) in 3 months and then checked again post-treatment for (DFI). The IVF/ICSI cycles will be analyzed for pregnancy outcomes

NCT ID: NCT04507022 Completed - Infertility Clinical Trials

The Outcome of Two Protocols Used to Prepare Endometrium for Frozen Embryo Transfer

Start date: August 12, 2020
Phase: Phase 4
Study type: Interventional

This is a RCT to test the outcome of two protocols used for preparation of the endometrium for frozen blastocyst embryo transfer

NCT ID: NCT04500522 Completed - Infertility, Female Clinical Trials

Vaginal Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy in Primarily Infertile Patients

Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

To compare the effectiveness of vaginal isonicotinic acid hydrazide with placebo in minimizing the pain experienced by primarily infertile patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.

NCT ID: NCT04500509 Completed - Infertility, Female Clinical Trials

Diclofenac Potassium With or Without Vaginal Dinoprostone Prior to Hysterosalpingography

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The aim of our study is to determine the efficacy of oral diclofenac potassium with or without vaginal dinoprostone prior to hysterosalpingography in primarily infertile patients on the pain scores during HSG.

NCT ID: NCT04500470 Completed - Infertility, Female Clinical Trials

Ketoprofen With or Without Vaginal Isonicotinic Acid Hydrazide Prior to Hysterosalpingography

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The aim of our study is to determine the efficacy of Ketoprofen with or without vaginal isonicotinic acid hydrazide on the pain scores during HSG.