Actively Recruiting

Phase Not Applicable
Age: 1Day - 3Months
All Genders
NCT06871995

Efficacy, Safety and Limitations of Spinal Block for All Infants Under 3 Months

Led by Ain Shams University · Updated on 2025-03-12

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Spinal anesthesia (SA) has been shown to be a viable alternative to general anesthesia (GA) for infants and children for a variety of surgical procedures. SA serves to avoid some of the potential risks of GA including the need for airway manipulation, hemodynamic instability, postoperative apnea, and exposure to medications that may cause neurotoxicity .SA allows the prevention and reduction of perioperative complications even if its duration is an important limiting factor. Because of this limitation, short surgery is the most indicated under SA . Premature infants and neurologically impaired children account for the majority of spinal anesthetics used today . This study evaluates the effectiveness, safety and limitations of spinal anesthesia when used for all infants under 3 months undergoing lower abdominal surgery at Ain Shams University Hospitals.

CONDITIONS

Official Title

Efficacy, Safety and Limitations of Spinal Block for All Infants Under 3 Months

Who Can Participate

Age: 1Day - 3Months
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age under 3 months
  • Physical status: American Society of Anesthesiologists I - II
  • Scheduled for elective lower abdominal surgeries such as hernia, hydrocele, or undescended testis
Not Eligible

You will not qualify if you...

  • Parents or legal guardian refuse the spinal anesthesia procedure
  • Bleeding disorders or use of anticoagulant or antiplatelet medications
  • Infection at the injection site

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine Ain Shams University

Cairo, Egypt

Actively Recruiting

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Research Team

A

ahmed ma Elewa mohamed, M.S.C

CONTACT

T

tarek Sa Shabana, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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