NCT07499817

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P25-P50 for phase_3

Timeline
Completed

Started Oct 2023

Typical duration for phase_3

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2023

Completed
2.5 years until next milestone

First Submitted

Initial submission to the registry

March 19, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 30, 2026

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

March 30, 2026

Status Verified

March 1, 2026

Enrollment Period

2.5 years

First QC Date

March 19, 2026

Last Update Submit

March 25, 2026

Conditions

Keywords

thawed embryoIVF

Outcome Measures

Primary Outcomes (1)

  • Pregnancy

    Beta-Human Chorionic Gonadotropin (β-hCG) was positive

    1 month

Study Arms (2)

(control)

ACTIVE COMPARATOR

received 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

Other: (control)

pentoxifylline 400 mg

EXPERIMENTAL

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.

Drug: pentoxifylline 400 mg

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.

Also known as: Trental ® Sanofi co.
pentoxifylline 400 mg

estradiol valerate 2 mg. in form of (Cycloprogynova® Bayer Shering Pharma) whitepills starting dose is one pill T.I.D

(control)

Eligibility Criteria

Age18 Years - 43 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Infertility

Interventions

Pentoxifylline

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Intervention Hierarchy (Ancestors)

TheobromineXanthinesPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Beni suef University

    Beni-Suef University

    PRINCIPAL INVESTIGATOR

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

Locations