Skip to content

clinical research of Digoxin in Patients With lymphocytic carcinoma

A Pilot Phase II Study of Digoxin in Patients With lymphocytic carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-13003369
Enrollment
Unknown
Registered
2013-07-23
Start date
2013-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

lymphocytic carcinoma

Interventions

only chemotherapy:chemotherapy
digoxin+chemotherapy:digoxin+chemotherapy

Sponsors

The Affiliated DrumTower Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patiens should meet all of the following requirement: 1. Patients diagnosised acute leukemia or diffuse large B cell lymphoma or indolent lymphoma; 2. Aged from 18y to 65y; 3. ECOG<2; 4. Signed informed consent and willing to follow-up visit.

Exclusion criteria

Exclusion criteria: Patiens should be excluded if she/he meet one of the following requirement 1. To be with arrhythmia history; 2. To be with hypertrophic obstructive cardiomyopathy history; 3. Pre-excitation syndrome syndrome associated with atrial fibrillation or flutter poorly controlled hypertension patients; 4. Serious electrolyte disturbances including serum K ,Ca, and Mg; 5. Women during pregnancy or lactation ,mental disorder; 6. Adequate liver and renal function within 2 weeks of Screening: 7. Bilirubin>14mg/LAlanine aminotransferase (ALT) or Aspartate aminotransferase (AST)> 2.0*the upper limit of normal (ULN); 8. creatinine clearance rate 265.2umol/L; 9. Alcohol abuse or drug abuse; 10. Involving in other clinical trial; 11. Allergy to digoxin; 12. Cardiac function > II grade or lung function >grade II.

Design outcomes

Primary

MeasureTime frame
os;PF;

Countries

China

Contacts

Public ContactOUYANG JIAN
oy626@sina.com+86 13770518202

Outcome results

None listed

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