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Phase II study of prophylactic oral administration of diltiazem for atrial fibrillation after lung resection

Phase II study of prophylactic oral administration of diltiazem for atrial fibrillation after lung resection - Prophylactic administration of diltiazem for atrial fibrillation after lung resection

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001691
Enrollment
124
Registered
2009-02-06
Start date
2009-01-01
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

atrial fibrillation after lung resection

Interventions

Diltiazem 90mg/day from POD 1 to POD 7 Diltiazem 60mg/day from POD 8 to POD 14 Lactose 0.9g/day from POD 1 to POD 7 Lactose 0.6g/day from POD 8 to POD 14

Sponsors

Department of Surgical Oncology, Hokkaido University Graduate School of Medicine
Lead Sponsor
Teine Keijinkai Hospital Minami Sanjo Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: primary lung cancer lobectomy or pneumonectomy PS 0-2 be able to take something by mouth WBC >3000 Hb >9.5 Plt >100000 T-bil <1.5 AST, ALT <80 Cre <1.5 PaO2 >65 or SpO2 >92 informed consent

Exclusion criteria

Exclusion criteria: unstable angina pectoris, myocardial infarction or heart failure with in 3 months uncontrolled diabetes or hypertension active infection gastrointestinal bleeding diarrhea ileus chronic Af already taking diltiazem or other calcium blocker AV block more than 2nd degree sick sinus syndrome past history of severe allergy uncontrolled pleural effusion, ascites or pericardial fluid in pregnancy

Design outcomes

Primary

MeasureTime frame
Incidence of atrial fibrillation after lung resection

Secondary

MeasureTime frame
Degree and frequency of adverse event (hypotension, bradycardia, etc.)

Countries

Japan

Contacts

Public ContactYasuhiro Hida

Hokkaido University Graduate School of Medicine Department of Surgical Oncology

011-706-7714

Outcome results

None listed

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