Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07465185

Intrathecal Bupivacaine With or Without Dexmetomidine for Cesserian Delivery

Intrathecal Bupivacaine With or Without Dexmetomidine for Cesserian Delivery ;Arandomized Non - Inferiority Study

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Benha University · Academic / Other
Sex
Female
Age
20 Years – 35 Years
Healthy volunteers
Not accepted

Summary

Cesarean section (CS) is one of the most frequently performed surgical procedures globally, with an increasing demand for safe and effective anesthesia techniques. Regional anesthesia, particularly intrathecal anesthesia, has become the method of choice for elective cesarean deliveries.The most commonly used local anesthetic for intrathecal anesthesia is bupivacaine.Recent studies have focused on adjunctive agents to enhance the efficacy of local anesthetics.

Conditions

Interventions

TypeNameDescription
DRUGBupivacainepatient will receive intra-thecal hyperbaric bupivacaine 11 mg(2.2 ml) of 0.5% bupivacaine, with 0.5 ml of normal saline in total volume 2.5 ml.
DRUGBupivacaine and Dexmedetomidinepatient will receive 9 mg (1.8 ml) of 0. 5% bupivacaine, with 5 μg of DEX in 0.5ml of normal saline in total volume 2.5 ml.

Timeline

Start date
2026-03-15
Primary completion
2026-09-15
Completion
2026-10-15
First posted
2026-03-11
Last updated
2026-03-11

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07465185. Inclusion in this directory is not an endorsement.