Skip to content

Comparison of Hydromorphone Extended Release Tablets after Titration with Morphine in the Treatment of Cancer Pain

After successful PCA titration of hydromorphone in patients with moderate to severe cancer pain, the conversion to hydromorphone sustained-release tablets was compared to maintenance therapy with morphine sustained-release tablets

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108512
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Cancer pain

Interventions

Morphine Extended Release Tablets Group:Morphine Extended Release Tablets
Hydromorphone sustained-release tablets group:Hydromorphone sustained-release tablets

Sponsors

Kunming Yan 'an Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The subjects voluntarily sign the informed consent form for this trial; 2. Patients diagnosed with malignant tumors by organization or pathology; 3. Age range of 18-80 years old, clear consciousness, regardless of gender; x; 4. Persistent cancer pain with NRS score >= 4 in the past 24 hours; 5. Patients who have not received radiation therapy within 7 days prior to randomization and trial; 6. ECOG-PS <= 3 points.

Exclusion criteria

Exclusion criteria: 1. The patient is diagnosed with non cancerous pain or unexplained pain; 2. Patients with paralytic intestinal obstruction; 3) Abnormal and clinically significant laboratory results, such as creatinine >= 2 times the upper limit of normal, ALT or AST >= 2.5 times the upper limit of normal (in patients with liver metastases or primary liver cancer >= 5 times the upper limit of normal), or Child C liver function; 4. Cognitive impairment; 5. Patients who are allergic to anesthetic drugs; 6. Pregnant or lactating patients; 7. Participate in drug trials (including the investigational drug) within one month prior to the trial; 8. Diseases and conditions that other researchers consider ineligible for inclusion.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with effective analgesia;Adverse reaction incidence rate;

Secondary

MeasureTime frame
Satisfaction evaluation;Quality of Life ;Proportion of patients with significant pain relief;Daily medication dosage;Daily frequency of pain outbreaks;

Countries

China

Contacts

Public ContactWanbao Ding

Kunming Yan 'an Hospital

1512044972@qq.com+86 13888894341

Outcome results

None listed

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