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NCT03436472

Dexmedetomidine and 5-year Outcome in Elderly Patients After Surgery

Completed NA Last updated 21 June 2019
What this trial tests

NA trial testing dexmedetomidine in Aged in 700 participants. Completed in 1 April 2019.

Timeline
1 June 2017
Primary endpoint
8 January 2019
1 April 2019

Quick facts

Lead sponsorPeking University First Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment700
Start date1 June 2017
Primary completion8 January 2019
Estimated completion1 April 2019
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University First Hospital

Who can join

Adults 65 to 90, any sex, with Aged or Operative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Delirium is a frequent postoperative complication. Its occurrence is associated with worse long-term outcomes. In a previous randomized controlled trial, prophylactic low-dose dexmedetomidine infusion during the early postoperative period decreased the incidence of delirium in elderly patients after surgery. The purpose of this 5-year follow-up study is to evaluate whether prophylactic low-dose dexmedetomidine infusion can improve the 5-year outcomes in elderly patients recruited in the previous randomized controlled trial.

Publications & conference data

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

Verify or expand the search:

Other trials of dexmedetomidine

Trials testing the same drug.

Other recruiting trials for Aged

Currently open trials in the same condition.

Other Peking University First Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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