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Comparing the effects of intravenous and epidural administration of dexmedetomidine on patients undergoing cesarean section under combined lumbar epidural anesthesia

Comparing the effects of intravenous and epidural administration of dexmedetomidine on patients undergoing cesarean section under combined lumbar epidural anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019100
Enrollment
Unknown
Registered
2018-10-25
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-11-26

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

Conditions

Cesarean section

Interventions

Group 1:Intravenous administration 1ug/kg dexmedetomidine
Group 2:Epidural administration 1ug/kg dexmedetomidine

Sponsors

Affiliated Hospital of Jinggangshan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists physical status I or II patients aged 18–45 years scheduled for elective cesarean sections (CSs) under spinal anesthesia (SA).

Exclusion criteria

Exclusion criteria: Patients with a primary core body temperature of more than 37.5 degree C or lower than 36.5 degree C, body mass index >25, with contraindications for SA, cardiac disease, history of psychiatric disease, taking a-receptor antagonist drugs, hypertensives, or any antihypertensive drug, renal failure, hepatic failure, a history of allergy to the study drugs, excessive hemorrhage needing transfusion, or failure or incomplete spinal block were excluded from the study.

Design outcomes

Primary

MeasureTime frame
Chills score;

Secondary

MeasureTime frame
Ramsay;Intraoperative Complications;Postoperative analgesia score;Postoperative defecation and exhaust time;

Countries

China

Contacts

Public ContactShu Liu

Affiliated Hospital of Jinggangshan University

ren1015787829@163.com+86 13979661067

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026