Dexmedetomidine infusion during general anesthesia for cesearian section

Effect of dexmedetomidine infusion on the depth of anesthesia and hemodynamics during general anesthesia for cesearian section

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201802003114191

Enrollment

Registered

2018-02-20

Start date

2016-10-20

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy and Childbirth Surgery depth of anesthesia Anaesthesia

Interventions

dexmedetomidine injection

group II

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: ¿Pregnant, full term women(completed 37 weeks). ¿Singleton pregnancy. ¿Patients ASA physical status I and II (American Society of Anesthesiologists Physical status ). ¿Patient refusal of regional anesthesia. ¿Infection at the site of injection of spinal anesthesia. ¿Surgical indication for general anesthesia.

Exclusion criteria

Exclusion criteria: ¿Refusal of participation in the study. ¿Allergy to dexmedetomidine. ¿Multiple pregnancy

Design outcomes

Primary

Measure	Time frame
effect of intraoperative dexmetomidine infusion on Bispectral index values	—

Secondary

Measure	Time frame
hemodynamics (heart rate,systolic and diastolic blood pressure);Apgar score ;Alderete score at post anesthetic care unit ;Sedation score ;Extra fentanyl 1 mcg/kg intravenously	—

Countries

Egypt

Contacts

Public Contactmokhtar amer

lecturer

mokhtaramer2000@yahoo.com00201111751673

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026