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Relationship Between Serum N/OFQ and Acute Myeloid Cell Leukemia

Relationship Between Serum N/OFQ and Acute Myeloid Cell Leukemia

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06469047
Acronym
RBSNAAMCL
Enrollment
80
Registered
2024-06-21
Start date
2024-06-20
Completion date
2024-12-31
Last updated
2024-06-21

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

Conditions

AML

Brief summary

Patients diagnosed with acute myeloid leukemia in the Second Hospital of Shanxi Medical University were selected and divided into the newly diagnosed group, the relapsed group, the complete remission group as the experimental group, and the healthy physical examination subjects as the control group. The relationship between IL-1β, catecholamine and norkephalin in peripheral blood of the experimental group and the control group was observed. According to the literature, the experimental group was significantly higher than the control group. In the experimental group, the newly diagnosed group was higher than the relapse group, and the relapse group was higher than the complete remission group, and the correlation was positive, and the difference was statistically significant.

Interventions

DIAGNOSTIC_TESTEnzyme-linked immunosorbent assay

Serum N/OFQ , IL-1β and NE levels were detected.

Sponsors

Second Hospital of Shanxi Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* In accordance with adult acute myeloid leukemia (non-acute promyelocytic leukemia)The diagnostic criteria for AML in the Chinese Diagnosis and Treatment Guidelines (2017 edition); ②Leukocyte count ≤ 25×109/L; * No treatment has been received in the past 6 months. * None of the candidates are related and known this study, and sign the informed consent.

Exclusion criteria

* Patients who are allergic to the drugs used in this study; * People with mental illness or cognitive impairment; * Patients with infectious diseases; ④Patients with severe heart, liver, kidney and other organ function lesions; ⑤ Combined with other malignant swelling. The tumor.

Design outcomes

Primary

MeasureTime frameDescription
N/OFQ24 hoursSerum N/OFQ levels
IL-1β24 hoursSerum IL-1β levels
NE24 hoursSerum NE levels

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026