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Clinical observation of butorphanol tartrate nasal spray in patients with multiple myeloma: a single-center study

Clinical observation of butorphanol tartrate nasal spray in patients with multiple myeloma: an IIT study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034792
Enrollment
Unknown
Registered
2020-07-19
Start date
2020-07-17
Completion date
Unknown
Last updated
2020-07-20

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

Conditions

Multiple myeloma

Interventions

The nasal spray group (N gruop):Butorphanol tartrate nasal spray, 1 spray each time (equivalent to 1 mg)

Sponsors

Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-70 years old; 2. Patients with multiple myeloma; 3. VAS score 3 to 6 points; 4. Patients with normal liver and kidney function; 5. Patients with normal ECG; 6. Patients without chemotherapy during medication; 7. Patients without PCIA.

Exclusion criteria

Exclusion criteria: 1. Patients known to be allergic to butorphanol or other research drugs; 2. Patients with long-term use of narcotic analgesics or non steroidal anti-inflammatory drugs; 3. Opioid dependent or opioid tolerant patients; 4. Patients with serious diseases of nasal mucosa; 5. Severe cardiac / circulatory dysfunction (systolic blood pressure >=180 mmHg and / or diastolic blood pressure >= 110 mmHg; systolic blood pressure 24 times / min), kidney (creatinine clearance rate <=30 ml/min); 6. Patients with mental disorders or other reasons that are difficult to cooperate with; 7. Patients taking stimulant CNS drugs or suffering from CNS disease or respiratory dysfunction at the same time; 8. Patients with a history of mental illness; 9. Patients who participated in other drug clinical studies in recent three months; 10. Subjects considered unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
pain score;

Secondary

MeasureTime frame
Ramsay;bruggrmann comfort scale;

Countries

China

Contacts

Public ContactLi Xiaoming

Department of Hematology, Affiliated Hospital of Southwest Medical University

lxm6358@21cn.com+86 13700986866

Outcome results

None listed

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