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NCT04711837 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of HSK3486 Compared to Propofol in Induction of General Anesthesia in Adults Having Elective Surgery

A Phase 3 study, sponsored by Haisco-USA Pharmaceuticals.

Completed
Registry status
Phase 3
Development phase
255
Enrollment target

NCT04711837: Completed Phase 3 study, sponsored by Haisco-USA Pharmaceuticals.

NCT04711837 is a Phase 3 study that has completed, run by Haisco-USA Pharmaceuticals. The registered enrollment target is 255 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04711837, a Phase 3 study, has completed, sponsored by Haisco-USA Pharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
255 participants
Enrollment target

Study Summary

This is a multicenter, randomized, double-blinded, propofol-controlled, Phase 3 clinical study to evaluate the efficacy and safety of HSK3486 for induction of general anesthesia in adults undergoing elective surgery.

Primary Outcome

The primary outcome of interest was the success rate of anesthesia induction, defined by the proportion of subjects with successful anesthesia. A subject was considered successful for anesthetic induction if the following conditions were met: induction success Modified Observer's Assessment of Awareness/Sedation Scale (MOAA/S ≤1) after administration of study drug and 1 or less top-up dose required without using any rescue drugs. Where Grade 0 is no response after trapezius squeeze, Grade 1 resp

Interventions

  • DRUG Propofol
  • DRUG HSK3486

Trial Details

FieldValue
Enrollment Target 255 participants
Start Date 2021-02-11
Est. Completion 2022-04-20
Phase Phase 3
Haisco-USA Pharmaceuticals

5 total trials

What the finished NCT04711837 record still lists

NCT04711837 is an interventional study that assigns participants to a tested intervention. The registered 255 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which Propofol is the first listed.

NCT04711837 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04711837 about?

NCT04711837 is a clinical study titled "Efficacy and Safety of HSK3486 Compared to Propofol in Induction of General Anesthesia in Adults Having Elective Surgery". This is a multicenter, randomized, double-blinded, propofol-controlled, Phase 3 clinical study to evaluate the efficacy and safety of HSK3486 for induction of general anesthesia in adults undergoing elective surgery.

What is the current status of trial NCT04711837?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 255 participants. The study started on 2021-02-11. Estimated completion is 2022-04-20.

What interventions are being tested in trial NCT04711837?

The interventions under investigation include: Propofol (DRUG), HSK3486 (DRUG).

Who is sponsoring clinical trial NCT04711837?

This trial is sponsored by Haisco-USA Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04711837's enrollment target sits among peer trials

255 1242nd of 2000 higher than 756 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04711837, the US trial registry maintained by the National Library of Medicine. NCT04711837 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.