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Clinical Study for Continuous Subcutaneous Infusion of Hydromorphone and Morphine in the Treatment of Moderate and Severe Cancer Pain

Clinical Study for Continuous Subcutaneous Infusion of Hydromorphone and Morphine in the Treatment of Moderate and Severe Cancer Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023310
Enrollment
Unknown
Registered
2019-05-22
Start date
2019-05-27
Completion date
Unknown
Last updated
2019-05-27

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

Conditions

Moderate and Severe Cancer Pain

Interventions

1:Hydromorphone
2:Morphine

Sponsors

Pain Management Department of West China Hospital Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Aged =18 years; 2) The patient with VAS=4 or breakthrough pain>3 times/day; 3) Oral equivalent morphine dose=60mg/d,unsatisfactory pain control; 4) The patient who can describe symptoms objectively and without serious infection.respiratory insufficiency,etc; 5) The patient without a history of drug abuse; 6) Non-pregnant&lactating women;the patient without a pregnancy plan within 1 month after the trial(including male); 7) The patient who did not participate in the drug test(including this drug) within 3 months before the test; 8) The patient volunteered to participate in this study.

Exclusion criteria

Exclusion criteria: 1) The patient who can not use subcutaneous administration; 2) Respiratory depression has shown purpura; 3) Allergic person,and the patient who suffered from allergic diseases or allergic to drugs similar in structure to the study drug; 4) Cognitive dysfunction; 5) The patient without morphine contraindications;the morphine contraindications such as Digestive tract perforation.Intestinal obstruction,etc; 6) Increased intracranial pressure and brain injury; 7) Bronchial Asthma; 8) Decompensated pulmonary heart disease; 9) Hypothyroidism; 10) Cortical insufficiency; 11) Prostatic hypertrophy,Dying dysuria; 12) Severe liver dysfunction; 13) Uncorrected shock.

Design outcomes

Primary

MeasureTime frame
Pain relief rate;VAS;

Secondary

MeasureTime frame
Number and extent of breakthrough pain;BPI;The satisfaction assessment of patient and medical staff;

Countries

China

Contacts

Public ContactHui Liu

Pain Management Department of West China Hospital Sichuan University

18980601547@qq.com+86 18980601547

Outcome results

None listed

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