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The effect of dexmedetomidine infusion during elective cesarean section on sleep quality on the night after surgery

The effect of dexmedetomidine infusion during elective cesarean section on sleep quality on the night after surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106212
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Sleep disorder

Interventions

Dexmedetomidine group:After the umbilical cord of the fetus was removed and severed, patients in the dexmedetomidine group received dexmedetomidine infusion, with a total dose of 0.5ug/kg completed wi
Control group :There were no intervention measures for patients in the control group

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
No minimum to 40 Years

Inclusion criteria

Inclusion criteria: 1. Sign the informed consent form; 2. No more than 40 years old; 3. ASA classification grades I to III; 4. Patients who are scheduled for an elective cesarean section.

Exclusion criteria

Exclusion criteria: 1. ASA> Grade III; 2. Has a history of dependence on painkillers; 3. Patients with dementia or cognitive dysfunction (positive CAM scale, MMSE scale score lower than 24 points); 4. Any cerebrovascular accident, such as stroke or transient ischemic attack (TIA), has occurred within three months 5. Anyone with communication difficulties.

Design outcomes

Primary

MeasureTime frame
Sleep quality scores;Edinburgh Postnatal Depression Scale score;

Secondary

MeasureTime frame
Pain scores;

Countries

China

Contacts

Public ContactJie Gao

The First Affiliated Hospital of Anhui Medical University

jgao-amu@163.com+86 551 6292 2344

Outcome results

None listed

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