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Pharmacokinetics and Pharmacodynamics of Dexmedetomidine applied to Patients undergoing General Anesthesia with End-stage Renal Failure and Hyperparathyroidism

Pharmacokinetics and Pharmacodynamics of Dexmedetomidine applied to Patients undergoing General Anesthesia with End-stage Renal Failure and Hyperparathyroidism

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-14005543
Enrollment
Unknown
Registered
2014-11-18
Start date
2013-04-01
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

End-stage Renal Failure and Insecondary Hyperparathyroidism

Interventions

end-stage renal failure and insecondary hyperparathyroidism Group:infusing Dexmedetomidine before anesthesia induction
General patient group:infusing Dexmedetomidine before anesthesia induction

Sponsors

Anesthesia Department of the second hospital of AnHui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Group E: Patients with end-stage renal failure and insecondary hyperparathyroidism, 18-65 years old, BMI less than 30 kg/m2, plan to implement parathyroidectomy and autotransplantation recently; Group C: Patients with no systemic disease,18-65 years old, BMI less than 30 kg/m2, plan to implement excision of adenoma of thyroid recently.

Exclusion criteria

Exclusion criteria: Patients who had serious cardiac, pulmonary hepatic, uncontrolled diabetes, such as difficult airway, asthma, Hepatitis B; gastrointestinal, neurologic, hematologic, or psychiatric disease; significant electrolyte imbalance; or uncontrolled hypo- or hyperthyroidism were excluded. Those with a particular history of disease, including alcohol and drug abuse, allergy of related medicine, taking anticonvulsants constantly, or having drugs which hindering the analysis of HPLC and hypotensors which effecting on alpha 2- adrenoreceptor (e.g. alpha-methyldopa, clonidine, guanfacine or Serpasil).

Design outcomes

Primary

MeasureTime frame
pharmacokinetics and pharmacodynamics;

Contacts

Public ContactZhang Ye
zhangye_hassan@sina.com+86 13966768081

Outcome results

None listed

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