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Study on the pharmacokinetics of cis-atracurium in the obese patients during anesthesia induction period.

Study on the pharmacokinetics of cis-atracurium in the obese patients during anesthesia induction period.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007221
Enrollment
Unknown
Registered
2015-10-15
Start date
2015-09-25
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

obesity

Interventions

obesity group:cis-Atracurium
normal control:cis-Atracurium

Sponsors

the First Affiliated Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Fifteen obese patients undergoing Laparoscopic Roux-en-Y gastric bypass were included. The inclusion criteria: aged 18 to 45 years with ASA class I or II, body mass index (BMI) >35kg/m2.

Exclusion criteria

Exclusion criteria: Preoperative exclusion criteria: hypertension, heart disease or any known muscle relaxant drug allergy history were excluded.

Design outcomes

Primary

MeasureTime frame
weigte;pharmacokinetic parameters;vital signs;—

Countries

China

Contacts

Public Contactxuemei Peng
31432507@qq.com+86 18928869988

Outcome results

None listed

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