Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 64Years
All Genders
NCT06949059

Intravenous Hydromorphone for the Treatment of Acute Pain

Led by The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School · Updated on 2025-11-17

30

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

T

The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Lead Sponsor

Y

Yichang Humanwell Pharmaceutical Co., Ltd., China

Collaborating Sponsor

AI-Summary

What this Trial Is About

To observe the efficacy and safety of hydromorphone in the treatment of acute chest pain, and to explore the potential advantages of hydromorphone for analgesia in patients with acute chest pain, so as to provide more theoretical basis for individualized analgesia and rapid recovery in patients with acute chest pain.

CONDITIONS

Official Title

Intravenous Hydromorphone for the Treatment of Acute Pain

Who Can Participate

Age: 18Years - 64Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-64 years old
  • Any gender
  • Acute chest pain with time from pain onset to doctor visit less than or equal to 24 hours
  • Severe pain requiring opioid use as determined by emergency physicians
  • Informed consent obtained from patient or family members
Not Eligible

You will not qualify if you...

  • Known allergy to hydromorphone or morphine
  • Systolic blood pressure less than 100 mmHg
  • Oxygen saturation less than 95%
  • Pulse rate less than 60 beats per minute
  • Use of acetaminophen or nonsteroidal anti-inflammatory drugs within the past 8 hours
  • Chronic pain lasting more than 12 weeks
  • Delirium, alcohol withdrawal symptoms, or other drug intoxication
  • Pregnant or lactating women
  • Mental or neurological diseases, cognitive or consciousness disorders preventing correct expression
  • Participation in another research study at the same time
  • Life-threatening chest pain requiring rapid diagnosis or treatment interventions such as resuscitation, or chest pain caused by myocardial infarction
  • Other factors increasing risk of study participation as judged by researchers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nanjing Drum Tower Hospital

Nanjing, Jiangsu, China, 210008

Actively Recruiting

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Research Team

H

Hao Sun, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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