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To investigate the effect of menstrual cycle on the sedative effect of dexmedetomidine in patients

To investigate the effect of menstrual cycle on the sedative effect of dexmedetomidine in patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15006092
Enrollment
Unknown
Registered
2014-09-11
Start date
2015-02-16
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

General Anesthesia

Interventions

the follicular group:Dexmedetomidine is intravenously administrated at a dose of 1.0ug/kg at 10 min intervals, then continuous infusion at 0.5 ug/kg/h for 20 min.
the luteal group:Dexmedetomidine is intravenously administrated at a dose of 1.0ug/kg at 10 min intervals, then continuous infusion at 0.5 ug/kg/h for 20 min.

Sponsors

Department of Anesthesia, Obstetrics and Genecology Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 40 female patients with regular menstrual cycles (a regular cycle was defined as lasting 25-35 days with no variations in the length of cycle of more than 2 days), ages 18–40 yr, ASA I–II, will be enrolled in the study.

Exclusion criteria

Exclusion criteria: irregular menstrual cycles; pregnancy; receiving hormones and medications that affected ovulation during the 6 weeks before surgery; chronic or acute (within 48 h) intake of psychotropic drugs; hepatic, renal, or neurological dysfunction; alcoholism or use of benzodiazepines, anticonvulsants, or opioids; In addition, those patients with a BMI 30 will also be excluded.

Design outcomes

Primary

MeasureTime frame
Bispectral Index;progesterone;oestrogen;

Countries

China

Contacts

Public ContactGE Shen-jin
shengjinge@163.com+86 13601926171

Outcome results

None listed

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