NCT06478199

Brief Summary

The aim of this study was to evaluate the relationship of seminal parameters with the neutrophil-to-lymphocyte ratio (NLR) and the platelet-to-lymphocyte ratio (PLR), which are inflammatory markers, in men with an abnormal semen analysis and men with normozoospermia.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
active not 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

January 1, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 24, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 27, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
Last Updated

January 17, 2025

Status Verified

January 1, 2025

Enrollment Period

1 year

First QC Date

June 24, 2024

Last Update Submit

January 14, 2025

Conditions

Fertility Issues

Outcome Measures

Primary Outcomes (1)

  • Laboratory result

    cbc and semen analysis

    1 day

Study Arms (2)

Group A :normal semen

Diagnostic Test: semen analysis

Group B : abnormal semen

Diagnostic Test: semen analysis

Interventions

semen analysisDIAGNOSTIC_TEST

lab invesigation

Also known as: cbc
Group A :normal semenGroup B : abnormal semen

Eligibility Criteria

Age18 Years+
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patient correlat to inclusion criteria

You may qualify if:

  • adult above 18 years primary not do varicocelectomy

You may not qualify if:

  • young secondry infertility recurrent varicocele

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kafrelsheikh University hospital

Kafr ash Shaykh, Egypt

Location

MeSH Terms

Conditions

Infertility

Interventions

Semen AnalysisBlood Cell Count

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Intervention Hierarchy (Ancestors)

Clinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisInvestigative TechniquesCell CountCytological TechniquesHematologic TestsCell Physiological PhenomenaBlood Physiological PhenomenaCirculatory and Respiratory Physiological Phenomena

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant lecturer of urology

Study Record Dates

First Submitted

June 24, 2024

First Posted

June 27, 2024

Study Start

January 1, 2024

Primary Completion

January 1, 2025

Study Completion

July 1, 2025

Last Updated

January 17, 2025

Record last verified: 2025-01

Locations

EG(1)