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NCT03741361

The Impact of Anxiety or Depression on the Sedative Concentration of Propofol

Completed Last updated 9 July 2019
What this trial tests

trial testing anxiety and depression in Anxiety in 120 participants. Completed in 15 February 2019.

Timeline
27 November 2018
Primary endpoint
1 February 2019
15 February 2019

Quick facts

Lead sponsorXuyu Zhang
StatusCompleted
Study typeOBSERVATIONAL
Enrollment120
Start date27 November 2018
Primary completion1 February 2019
Estimated completion15 February 2019
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Xuyu Zhang

Who can join

Adults 18 to 65, female only, with Anxiety or Depression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

120 consecutive female patients, 18-65 years old, American Society of Anesthesiologists (ASA) physical status I to II, scheduled for hysteroscopic surgery under propofol-based intravenous anesthesia will be recruited in this cohort study. The day before surgery, participants will be assessed the state of preoperative anxiety and depression. On the day of surgery, propofol will be administered by target controlled infusion (TCI) pump. During induction of anesthesia, the level of sedation will be evaluated. The induction dose of propofol, target effect-site concentration(Cet), plasma concentration(Cp) and effect-site concentration (Ce) of propofol will be recorded.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Anxiety

Currently open trials in the same condition.

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Data sources for this page

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