← Back to Clinical Trials
Recruiting NCT07154134

NCT07154134 Endocan and Copeptin Serum Levels in Preterm Neonates With Respiratory Distress Syndrome

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07154134
Status Recruiting
Phase
Sponsor Tanta University
Condition Endocan
Study Type OBSERVATIONAL
Enrollment 40 participants
Start Date 2025-07-10
Primary Completion 2025-11-01

Eligibility & Interventions

Sex All sexes
Min Age 28 Weeks
Max Age 36 Weeks
Study Type OBSERVATIONAL
Interventions
Serum endocanSerum copeptin

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 40 participants in total. It began in 2025-07-10 with a primary completion date of 2025-11-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This work aims to investigate and compare the levels of serum endocan and serum copeptin on the first day of life and correlate their levels to the severity of respiratory distress in preterm neonates suffering from respiratory distress syndrome.

Eligibility Criteria

Inclusion Criteria: * Prematurity. * Gestational age between 28 and 36 weeks. * Suffering from respiratory distress syndrome. Exclusion Criteria: * Intrauterine growth restriction (IUGR). * Hypoxic ischemic encephalopathy. * Multiple congenital anomalies. * Chromosomal abnormalities. * Preterm less than 28 weeks. * Neonates with a maternal history of chorioamnionitis (early sepsis). * Infant of diabetic mother. * Prelabor rupture of membranes (PROM)\> 2 hours.

Contact & Investigator

Central Contact

Asmaa M Elmesiry, MD

✉ asmaa.elmesery@med.tanta.edu.eg

📞 00201224285567

Frequently Asked Questions

Who can join the NCT07154134 clinical trial?

This trial is open to participants of all sexes, aged 28 Weeks or older, up to 36 Weeks, studying Endocan. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07154134 currently recruiting?

Yes, NCT07154134 is actively recruiting participants. Contact the research team at asmaa.elmesery@med.tanta.edu.eg for enrollment information.

Where is the NCT07154134 trial being conducted?

This trial is being conducted at Tanta, Egypt.

Who is sponsoring the NCT07154134 clinical trial?

NCT07154134 is sponsored by Tanta University. The trial plans to enroll 40 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology