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NCT03603873

Preoperative Anxiety Level, Premedications and General Anaesthetic Proceedings

Completed Last updated 27 July 2018
What this trial tests

trial in Anxiety in 1,200 participants. Completed in 24 May 2017.

Timeline
3 March 2017
Primary endpoint
24 May 2017
24 May 2017

Quick facts

Lead sponsorCHU de Reims
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,200
Start date3 March 2017
Primary completion24 May 2017
Estimated completion24 May 2017
Sites1 location across France

Conditions studied

Sponsor

CHU de Reims — full company profile →

Who can join

18 and older, any sex, with Anxiety or Premedication. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Although it seems obvious that the high level of preoperative anxiety may affect intraoperative anaesthetic requirements and recovery adversely, there are several contradictory studies about this subject. Furthermore, the effects of anxiolytic premedication are actually disputed: sedative premedication is widely administered but little clinical evidence supports its use. We want to evaluate the effects of pre-procedure anxiety for propofol needs in patients receiving general anaesthetic procedure. We also want to know if premedication is useful according to the preoperative anxiety level, in order to determine if a sub-group of patients benefit from it.

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.

Other CHU de Reims trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03603873.

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