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The comparison of dexmedetomidine and propofol used in upper gastrointestinal endoscopy

The comparison of dexmedetomidine and propofol used in upper gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005690
Enrollment
Unknown
Registered
2014-12-18
Start date
2014-12-25
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

anesthesia and analgesia

Interventions

Dexmedetomidine Group:Patients receiving dexmedetomidine 1 ug/kg for 10 min followed by 0.5 ug/kg.h until the end of the examination
fentanyl methord group:fentanyl methord 0.6 mg/kg i.v., plus 10~20mg if necessary

Sponsors

Department of Anesthesiology, the Second Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients of either sex, aged eighteen to sixty-five years old for elective EGD procedure, with American Society of Anaesthesiologist (ASA) Grade I and II were included.

Exclusion criteria

Exclusion criteria: Patients with ASA physical status Grade III and more, prior gastrectomy, patients with comorbid conditions such as diabetes mellitus, cardiovascular disease, hepatic or renal insufficiency, history of chronic alcoholism, sedative and narcotic analgesic drug abuse; allergy to any of the drugs such as opioids, dexmedetomidine, egg or soya bean, uncooperative and pregnant patient were also excluded.

Design outcomes

Primary

MeasureTime frame
Mean Arterial Pressure;Heart Rate;Respiratory Rate;hemoglobin oxygen saturation;

Secondary

MeasureTime frame
sedation level at the mid-procedure;Sedation Levle;number of patients needed additional propofol;number of patients recovered 15 min after the procedure;number of patients recovered 30 min after the procedure;number of patients who recovered more than 30 min after the procedure;number of patients gagging;number of patients suffering bradycardia;number of patients suffering respiratory depression;satisfactory score of patients;

Countries

China

Contacts

Public ContactYun Wu
wuyunanyi@163.com+86 13865958254

Outcome results

None listed

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