Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
NCT05809180

Pro-miniCHOP-like Regimen for Treatment-naive Elderly Patients

Led by The First Affiliated Hospital of Soochow University · Updated on 2023-04-20

35

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The proposed study is a prospective, single-center and open-ended study in patients over the age of 70 with treatment-naive diffuse large B-cell lymphoma (DLBCL). This study intends to explore a new treatment pattern using Pro-miniCHOP-like regimen and simultaneously evaluate its safety and efficacy for future clinical practice.

CONDITIONS

Official Title

Pro-miniCHOP-like Regimen for Treatment-naive Elderly Patients

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histopathologically or cytologically confirmed newly diagnosed untreated diffuse large B-cell lymphoma (DLBCL)
  • At least one measurable lesion of 15 mm or larger on imaging
  • Age 70 years or older
  • Life expectancy longer than 3 months
  • Adequate organ function: liver enzymes, bilirubin, and creatinine less than 3 times the upper limit of normal; cardiac ejection fraction 50% or higher; oxygen saturation above 90% without oxygen support
  • Signed informed consent obtained
Not Eligible

You will not qualify if you...

  • Severe liver or kidney dysfunction with enzyme or creatinine levels more than 3 times the upper limit of normal
  • Symptomatic or significant heart disease (NYHA class 2 or higher)
  • Uncontrolled active infection
  • Central nervous system involvement of DLBCL
  • History of blood vessel clots
  • Presence of other active tumors
  • Need for systemic corticosteroid treatment
  • Psychological conditions preventing study participation or informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

the First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China, 215006

Actively Recruiting

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Research Team

Z

Zhengming Jin

CONTACT

C

Changju Qu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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