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A pilot study to examine the safety of combination with selective COX2 inhibitor meloxicam before autologous peripheral blood stem cell harvest and the collection efficiency of hematopoietic stem cells

A pilot study to examine the safety of combination with selective COX2 inhibitor meloxicam before autologous peripheral blood stem cell harvest and the collection efficiency of hematopoietic stem cells - The safety of meloxicam before autologous PBSCH and the collection efficiency of hematopoietic stem cells

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027600
Enrollment
5
Registered
2017-06-02
Start date
2016-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients with multiple myeloma who receive autologous peripheral blood stem cell harvest

Interventions

Patients are administered meloxicam 10 mg once per day from the 10th day after the administration of the anticancer drug until 2 days before apheresis

Sponsors

Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients who receive their first autologous peripheral blood stem cell harvest 2)Patients who are eligible for apheresis 3)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Patients who are not eligible for apheresis 2)Allergy to meloxicam 3)Patients who cannot take medicine orally on the 10th day after the administration of the anticancer drug 4)Patients with bleeding tendency before treatment 5)Patients who are difficult to maintain platelets more than 20,000/mm3 even if appropriate measures such as platelet transfusion are done 6)Patients with active gastrointestinal ulcer 7)Patients with severe renal dysfunction (G3b or more in GFR classification) 8)Patients with aspirin-induced asthma or a history of aspirin-induced asthma 9)Inadequate condition as diagnosed by primary physician

Design outcomes

Primary

MeasureTime frame
Cumulative incidence and severity of bleeding, gastrointestinal ulcer and renal dysfunction and analgesic effect

Secondary

MeasureTime frame
The collection efficiency of hematopoietic stem cells

Countries

Japan

Contacts

Public ContactAiko Igarashi

Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital Hematology division

aikochan@muc.biglobe.ne.jp03-3823-2101

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026