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Efficacy and safety of hydromorphone hydrochloride for emergency analgesia

Clinical observational study of hydromorphone hydrochloride for emergency analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088376
Enrollment
Unknown
Registered
2024-08-16
Start date
2023-10-21
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute pain

Interventions

experimental group:Hydromorphone hydrochloride injection

Sponsors

the Third People's Hospital of Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1)patients with acute moderate to severe pain (NRS = 4) requiring opioid analgesic treatment; 2) adult patients (aged = 18 years); 3)obtained informed consent from the patient.

Exclusion criteria

Exclusion criteria: 1) pregnant or lactating women; 2) allergic to opioids including hydromorphone or butorphanol; 3) chronic use of opioids or a history of opioid addiction; 4) presence of medical conditions that may affect the metabolism of opioid analgesics (severe hepatic or renal insufficiency); 5) systolic blood pressure less than 90 mmHg, heart rate less than 50 beats/min, or oxygen saturation less than 90% on room air; 6) intoxication by alcohol or other drugs; 7) presence of symptoms of respiratory depression, suffering from acute or severe bronchial asthma; 8) presence or risk of progression to gastrointestinal obstruction, especially paralytic intestinal obstruction; 9) loss of hearing or vision, or any other condition that may substantially interfere with the collection of data for the study; 10) communication deficits (e.g. psychiatric or neurological disorders or sedation); 11) use of opioids within the previous 24 hours; 12) any medication that might interact with one of the study medications; 13) had participated in this study or concurrently participated in any clinical trial.

Design outcomes

Primary

MeasureTime frame
Pain relief rate;Time to achieve analgesia;

Secondary

MeasureTime frame
Incidence of adverse reactions;pain locations;The proportion of target analgesia score achieved at each time point;Additional analgesics and dosage;Total analgesic dose;Length of stay in the emergency department;the blood pressure, heart rate, respiratory rate , and pulse oxygen saturation ;

Countries

China

Contacts

Public ContactXiang Tao

the Third People's Hospital of Chengdu

xt1142752929@126.com+86 138 8213 2616

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026