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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05971667
Other study ID # Tadalafil IVF
Secondary ID
Status Not yet recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date July 30, 2023
Est. completion date October 30, 2023

Study information

Verified date August 2023
Source Beni-Suef University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the Effect of different vasodilators as Tadalafil, Sildenafil and pentoxyfylline in In vitro Fertilization. In addition, the thickness of endometrium and pregnancies rates of these women will also be examined. All adverse effects of all drugs will be estimated


Description:

A prospective randomized clinical study will be conducted in the IVF clinic of the gynecology department of Beni Suef University Hospital, Beni-Suef, Egypt. The study will These patients will be randomized into four groups. The participants will take drugs starting from the end of menstruation cycle till endometrium reach optimal and then will start progesterone 800 mg daily.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date October 30, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - women having thawed embryos Exclusion Criteria: - hypotension - cardiovascular, hepatic, and renal diseases; - uncontrolled diabetes mellitus; - ovarian cysts; - hyperprolactinemia; - abnormal thyroid functions; - uterine fibroids; - patients taking nitrates; - endometriosis and adenomyosis

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
tadalafil
tadalafil 10 mg one tablet daily
Sildenafil
sildenafil 20 mg two tablets daily
pentoxifylline
pentoxifylline 400 mg two tabs daily

Locations

Country Name City State
Egypt Beni-suef university Hospital Bani Suwayf Beni Suef

Sponsors (1)

Lead Sponsor Collaborator
Beni-Suef University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary endometrial thickness measured by transvaginal ultrasound within 16 day of menstruation
Secondary pregnancy rate number of cases positive serum pregnancy test 1 month
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