Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04283435
Other study ID # PROTOCOL 500
Secondary ID
Status Not yet recruiting
Phase Phase 1
First received
Last updated
Start date September 1, 2021
Est. completion date March 1, 2022

Study information

Verified date August 2021
Source Cairo University
Contact Eman Elkattan, MD
Phone 01212529213
Email emyelkattan@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Management of Thin endometrium in IVF is challenging. Thin endometrium is often defined as <7 mm or < 8 mm on the day of Human Gonadotropin administration(Bu and Sun, 2015; Wu et al., 2014). Its incidence is 1-2.5% in most studies ( AlGhamdi et al.,2008). Endometrial thickness and endometrial vascularity is closely linked to endometrial receptivity.Improving endometrial receptivity is a predictor of the success in IVF. Many medications have been tried to improve endometrial thickness as Aspirin,sildenafil citrate,luteal estradiol and Granulocyte colony stimulating factor. Nitric oxide (NO) is a key signaling molecule involved in the vasodilator response of smooth muscle cells. NO activates the cyclic guanosine monophosphate (cGMP)/protein kinase G (PKG) pathway within smooth muscle cells to promote smooth muscle cell relaxation. Sildenafil citrate inhibits phosphodiesterase 5 (PDE5) maintaining activation of cGMP and PKG and maximizing the effect of existing NO, thus facilitating smooth muscle cell relaxation. The potent vasodilator action of sildenafil has led researchers to evaluate sildenafil as a treatment in assisted reproduction where low uterine blood flow is perceived to be a contributor to implantation failure (Fairouzabadi et al.2013). The investigators aim at this study to investigate the role of sildenafil citrate on endometrial and subendometrial vasculature in women with thin endometrium undergoing Frozen-Thawed IVF cycles.


Description:

This is a Randomised-controlled trial .The investigators recruited 100 women who are known to have thin endometrium in previous IVF cycles (failed/cancelled cycles). They are randomised into group A (50 women) : preparation of the endometrium with Estradiol valerate 2mg/day (every 8 hours)(white tablets of cycloprogenova,Payer,Germany) from the first day of the cycle till 12th day and The investigators add placebo from the first day of the cycle till the day of starting progesterone (It will be stopped 3 days before embryo transfer).Group B (50 women): The investigators add Sildenafil citrate (Viagra,pfizer,United states) to the estradiol valerate. Sildenafil 50 mg will be used daily from the first day of the cycle till the day of starting progesterone (It will be stopped 3 days before embryo transfer). The embryos will be transferred depending on their age on day 3 or day 5. At the transfer date ,the investigators will assess the endometrial thickness, endometrial volume, uterine artery doppler indices (RI,PI) as well as 3D endometrial vascular indices (VI,FI,VFI) .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 40 Years
Eligibility Inclusion Criteria: - Women (25 -40 years) undergoing IVF frozen-Thawed cycles and known to have good quality embryos. - previous thin endometrium (< 8mm on at least 3 previous cycles) with normal Hysteroscopy findings Exclusion Criteria: - women less than 25 years old or more than 40 years old. - abnormal hysteroscopic findings. - women with congenital uterine anomalies. - History of previous uterine surgery - Any contraindication to Sildenafil as Previous history of cardiac disease or stroke.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Sildenafil Citrate
Sildenafil Citrate 50 mg tablets taken from the first day of the cycle till the day we start progesterone (we stop 3 days before embryo transfer)
Other:
Placebo
Placebo tablet (multivitamins),Pregnacare vitamins (Vitabiotics,UK)
Drug:
Estradiol Valerate
Estradiol valerate tablets 2mg every 8 hours daily starting from the fist day of the cycle till 12th day of the menstrual cycle.

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical Pregnancy rate 2 weeks after embryo transfer
Secondary endometrial thickness at the time of embryo transfer
Secondary Endometrial volume at the time of embryo transfer
Secondary Uterine artery doppler indices at the time of embryo transfer
Secondary 3D endometrial and subendometrial vascular indices(VI,FI.VFI) at the time of embryo transfer
See also
  Status Clinical Trial Phase
Recruiting NCT05969574 - Is Decreased Ovarian Reserve Related to an Increased Number of Previous Early Miscarriages?
Completed NCT04778358 - Higher Dose of Rekovelle in Oocyte Donors Phase 2
Completed NCT04052464 - The Study of the Implantation Window From Endometrial Biopsy With Gene Expression Methods
Completed NCT04108039 - Micronized Progesterone vs Gonadotropin-releasing Hormone (GnRH) Antagonist in Freeze-all IVF Cycles. N/A
Suspended NCT04669652 - Evaluating Piezo-ICSI. - The EPI Study. N/A
Completed NCT04524026 - RIOTC: Reducing the Impact of Ovarian Stimulation. Novel Approaches to Luteal Support in IVF-Study 2 Phase 2
Recruiting NCT05981898 - Opt-IVF Multi-center Trial 2 Including All Protocols N/A
Recruiting NCT05737381 - Quality of Human Embryos in IVF, Culturing in Differentiated Oxygen N/A
Recruiting NCT04447872 - The LUTEAL Trial: Luteal Stimulation vs. Estrogen Priming Protocol N/A
Completed NCT04425317 - Detection of SARS-CoV-2 in Follicular Fluid and Cumulus-oocyte-complexes in COVID-19 Patients N/A
Not yet recruiting NCT05932082 - The Impact of Myomectomy on IVF Outcomes N/A
Recruiting NCT04654741 - The Rate of Embryo Euploidy in Progestin-primed Ovarian Stimulation Cycles Phase 4
Completed NCT04099784 - Health of Frozen Transferred Versus Fresh Transferred Children
Recruiting NCT05788822 - MVA to Improve the Pregnancy Outcome in Aged Infertility Women With Assisted Reproductive Technology N/A
Completed NCT04956848 - Comparing KIDScoreā„¢ D5 and iDAScore®. The KiDA Study N/A
Not yet recruiting NCT06048666 - Platelet Rich Plasma on Ovarian Reserve Parameters and Intra Cytoplasmic Sperm Injection Outcomes in Patients With Diminished Ovarian Reserve Phase 3
Not yet recruiting NCT05954962 - Efficacy of Micronized Natural Progesterone vs GnRH Antagonist in the Prevention of LH Peak During Ovarian Stimulation. Phase 4
Not yet recruiting NCT02698488 - Embryo Selection by Metabolomic Profiling of Embryo Culture Medium With Mass Spectroscopy as an Adjunct to Morphology N/A
Completed NCT01385618 - Gene-polymorphisms Relating to Human Subfertility N/A
Recruiting NCT05893238 - Human Follicular Fluid Markers and Reproductive Outcomes in IVF