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NCT04111328

the Effect of Different Drugs and Infusion Ways on Degree of Postoperative Comfort

Completed Phase 4 Last updated 9 February 2021
What this trial tests

Phase 4 trial testing intravenous sufentanil in Analgesia, Patient-Controlled in 600 participants. Completed in 30 October 2020.

Timeline
8 October 2019
Primary endpoint
30 September 2020
30 October 2020

Quick facts

Lead sponsorJun Wang
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment600
Start date8 October 2019
Primary completion30 September 2020
Estimated completion30 October 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Jun Wang — full company profile →

Who can join

Adults 18 to 65, any sex, with Analgesia, Patient-Controlled. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To explore the effect of different drugs and infusion ways on degree of postoperative comfort.Patients undergoing spinal neoplasm surgery receive different patient controlled analgesia(PCA) drugs postoperatively,one group is sufentanil,the other is hydromorphone. Then each drug group will be divided into two subgroups according to the infusion way,intravenously,subcutaneously. During the patient controlled analgesia period, patients' degree of comfort,pain score,sleep quality, the degree of side reaction 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 trials of intravenous sufentanil

Trials testing the same drug.

Other recruiting trials for Analgesia, Patient-Controlled

Currently open trials in the same condition.

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