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CompletedNCT06788704Updated Jan 28, 2025

Tadalafil Daily Used Post Turp

An observational study in Erectile Dysfunction Following Urethral Surgery, sponsored by Kafrelsheikh University. Completed at 1 site in Egypt. Open to male participants. Per ClinicalTrials.gov, last updated 2025-01-28.

Sponsored by Kafrelsheikh University · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
270
Sex
Male
01

Study summary

to assess the effect of early tadalafil 5 mg once daily on persistent storage lower urinary tract symptoms (LUTS) and erectile function after transurethral resection of the prostate (TURP).

02

Conditions studied

  • Erectile Dysfunction Following Urethral Surgery

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03

In context

Erectile Dysfunction

683 studies on the registry are indexed under Erectile Dysfunction; 117 are open to participants now.

This study's enrollment of 270 is above the median of 130 across 115 observational studies indexed under Erectile Dysfunction.

Browse Erectile Dysfunction studies →

Lead sponsor

Kafrelsheikh University is the lead sponsor of 285 studies on the registry; 110 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Sampling method
Probability sample

Study population

Sexual active male patients underwent TURP

Inclusion criteria

  • sexual active men

Exclusion criteria

Exclusion Criteria:

  • sexual inactive men
  • cardiac patients
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
270 participants (actual)
Patient registry
No

Groups and cohorts

  • Patient recive tadalafil 5mg once daily early post turp

    Drug: Tadalafil 5mg

  • Patient recive placebo once daily early post turp

    Drug: Placebo

Interventions

  • DrugTadalafil 5mg

    Patient recive tadalafil 5mg once daily early post turp

  • DrugPlacebo

    Patient recive placebo once daily early post turp

06

What researchers measure

Primary outcomes

  1. Assess erectile function

    Using IIEF score

    Time frame: One month

  2. Assess erectile function

    Usine IIEF score

    Time frame: 3 month

Secondary outcomes

  1. Assess storage symptoms

    Using IPSS Score

    Time frame: One month

  2. Assess storage symptoms

    Using IPSS score

    Time frame: 3 month

07

Study locations

1 site
  • Elsayed Abdelhalim Elsayed
    Zagazig, 44749, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06788704
Lead sponsor
Kafrelsheikh University
Responsible party
Elsayed Abdelhalim Elsayed (assistant lecturer of urology, Kafrelsheikh University) — Principal investigator
First posted
Jan 23, 2025
Start date
May 1, 2021
Primary completion
Oct 1, 2022
Completion
Oct 1, 2022
Last update
Jan 28, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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