Effect of Pentoxyfilline on Endometrial Thickness and Frozen Embryo Transfer Outcomes
1 other identifier
interventional
100
1 country
1
Brief Summary
The aim of this work was to investigate the effect of different vasodilators as pentoxifylline in women with unexplained infertility using IVF
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_3
Started Oct 2023
Typical duration for phase_3
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2023
CompletedFirst Submitted
Initial submission to the registry
March 19, 2026
CompletedFirst Posted
Study publicly available on registry
March 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedMarch 30, 2026
March 1, 2026
2.5 years
March 19, 2026
March 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pregnancy
Beta-Human Chorionic Gonadotropin (β-hCG) was positive
1 month
Study Arms (2)
(control)
ACTIVE COMPARATORreceived estradiol valerate 2 mg. in form of (Cycloprogynova® Bayer Shering Pharma) white pills starting dose is one pill T.I.D may be increased to two pills T.I.D according to endometrial5 thickness in day 9 measured by vaginal ultrasound
pentoxifylline 400 mg
EXPERIMENTALOnce daily in form of (Trental ® Sanofi co.) daily in addition to the above treatment protocol from the first day of the cycle until the day of starting progesterone.
Interventions
Once daily in form of (Trental ® Sanofi co.) daily in addition to the above treatment protocol from the first day of the cycle until the day of starting progesterone.
estradiol valerate 2 mg. in form of (Cycloprogynova® Bayer Shering Pharma) whitepills starting dose is one pill T.I.D
Eligibility Criteria
You may qualify if:
- as good quality day five frozen embryos.
You may not qualify if:
- history of endocrine diseases,
- history of any previous surgery that couldm compromise the integrity of endometrium,
- cardiovascular, renal and liver diseases,
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beni-suef university Hospital
Banī Suwayf, Beni Suweif Governorate, 62521, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Beni suef University
Beni-Suef University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of obstetrics and gynecology
Study Record Dates
First Submitted
March 19, 2026
First Posted
March 30, 2026
Study Start
October 1, 2023
Primary Completion
April 1, 2026
Study Completion
April 30, 2026
Last Updated
March 30, 2026
Record last verified: 2026-03