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Comparison of the effectiveness of four ultrasonography-guided methods for median cubital vein puncture in obese patients undergoing ozone autohemotherapy.

Comparison of the effectiveness of four ultrasonography-guided methods for median cubital vein puncture in obese patients undergoing ozone autohemotherapy.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100948
Enrollment
Unknown
Registered
2025-04-17
Start date
2024-07-04
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Obesity

Interventions

Single developing line group (U):Tie a developing line to the ultrasound probe and place the ultrasound probe so that the developing line is located in the middle of the median cubital vein. Then al
Double developing line group (D):The two shadow lines were tied to the ultrasound probe so that the inner diameter of the double shadow line = the outer diameter of the ozonated autohemotherapy punctu
Median line group (M):The ultrasound median line is displayed, the ultrasound probe is placed so that the median line is located in the middle of median cubital vein, the puncture needle is aligned wi
Standard out-of-plane puncture group (U):Classical conventional out-of-plane ultrasound-guided puncture of the median cubital vein, without any visualization or localization line guidance. Entering th

Sponsors

the First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 - 80 years old. 2. BMI >= 30kg/m^2 3. Need to perform triple oxygen autohemotherapy. 4. No skin injury, infection, swelling or nodule in the puncture area. 5. ASA I-III. 6. Comply with the indications of the expert consensus on trioxane autologous blood transfusion;

Exclusion criteria

Exclusion criteria: 1. anatomical abnormalities at the puncture site; 2. puncture site infection, hematoma, or severe systemic infection; 3. glucose-6-phosphate dehydrogenase deficiency (serosanguineous disease); and 4. toxic diffuse goiter (Graves' disease). 5. thrombocytopenia less than 50 x 10^9/L or severe coagulation disorders; and 6. severe unstable cardiovascular disease or acute myocardial infarction; and 7. Acute alcohol intoxication 8. massive blood loss, acute bleeding, anemia (<90g/L); and 9. water and electrolyte disorders; and 10. Epileptic seizures 11. Hemochromatosis, patients treated with copper or iron; and 12. Anticoagulant (sodium citrate) allergy. 13. Pregnancy 14. Severe hepatic insufficiency;

Design outcomes

Primary

MeasureTime frame
First puncture success rate ;

Secondary

MeasureTime frame
Time to first successful puncture;Time to twice successful puncture;The second puncture was more successful than;Secondary puncture success ratio;Total successful puncture time;positioning time;Average number of punctures;

Countries

China

Contacts

Public ContactXiaokai Zhou

the First Affiliated Hospital of Nanjing Medical University

orthoxiaokaizhou@163.com+86 137 7052 7630

Outcome results

None listed

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