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The effect of titration treatment of moderate to severe cancer pain with hydromorphine hydrochloride sustained-release tablets combined with morphine hydrochloride tablets and its influence on sleep quality

The effect of titration treatment of moderate to severe cancer pain with hydromorphine hydrochloride sustained-release tablets combined with morphine hydrochloride tablets and its influence on sleep quality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104028
Enrollment
Unknown
Registered
2025-06-10
Start date
2025-06-18
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Moderate to severe cancer pain

Interventions

Control group:Titration was carried out using morphine hydrochloride tablets alone
Experimental group:Hydromorphine hydrochloride sustained-release tablets were added on the basis of the control group

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient meets the diagnostic criteria for moderate to severe cancer pain in the "Diagnosis and Treatment Specifications for Cancer Pain". 2. The patient has no tolerance to opioid drugs; 3. During the entire period of this therapeutic effect evaluation, the patient did not undergo radiotherapy or chemotherapy. 4. The patient is expected to survive for more than two months.

Exclusion criteria

Exclusion criteria: 1. Exclude those with severe functional disorders of organs such as the heart; 2. Exclude those with contraindications to opioid drugs such as headache, respiratory depression or paralytic intestinal obstruction.

Design outcomes

Primary

MeasureTime frame
Pain relief situation;

Secondary

MeasureTime frame
sleep quality;Adverse reactions;

Countries

China

Contacts

Public ContactFeng Xiaobo

Zhongnan Hospital, Wuhan University

fengxb@whu.edu.cn+86 189 8612 0410

Outcome results

None listed

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