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Effect of intraoperative dexmedetomidine on post-craniotomy pain

Effect of intraoperative dexmedetomidine on post-craniotomy pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003598
Enrollment
Unknown
Registered
2013-09-16
Start date
2013-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

anesthesia of neurosurgery

Interventions

dexmedetomidine group:dexmedetomidine group

Sponsors

Department of Anesthesiology, First Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients between the ages of 18 and 65 years with ASA classification17 of I or II undergoing craniotomy were eligible for inclusion in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria were known allergy to a-2 agonists, obesity, ASA classification III or more, cardiac abnormalities, craniofacial anomaly, respiratory problems (pneumonia, asthma, bronchitis and severe obstructive sleep apnea), Glasgow Coma Scale (GCS)<15, intracranial hypertension and uncontrolled epilepsy.

Design outcomes

Primary

MeasureTime frame
hemodynamic changes;pain scores;

Secondary

MeasureTime frame
PONV scores;satisfaction score;

Countries

China

Contacts

Public ContactKe Peng

Department of Anesthesiology, First Hospital of Soochow University,

pengke0422@163.com+86 15962155989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 18, 2026