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Recruiting NCT03647072

PPI Versus Histamine Antagnists as Adjuvant to Chemotherapy

Phase III Interventional Lymphoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CHOP, CHOP Plus Lanzoprazole, CHOP Plus Famotidine.
Who it may be relevant to
Registry conditions: Lymphoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparative Clinical and Biochemical Study Evaluating the Effect of Proton Pump I Nhibitors Versus Histamine 2 Receptor Antagonists as an Adjuvant With Chemotherapy in Patients With Non-hodgkin Lymphoma.

Overview

The study is a Comparative Clinical and Biochemical Study Evaluating the effect of Proton Pump I nhibitors versus histamine 2 Receptor antagonists as an adjuvant with chemotherapy in patients with Non-hodgkin Lymphoma.

Detailed description

The study is a Comparative Clinical and Biochemical Study Evaluating the effect of Proton Pump Inhibitors versus histamine 2 Receptor antagonists as an adjuvant with chemotherapy in patients with Non-hodgkin Lymphoma to compare the difference in efficacy.

Interventions

  • Drug CHOP
    CHOP only
  • Drug CHOP Plus Lanzoprazole
    CHOP plus Lanzoprazole 60 mg
  • Drug CHOP Plus Famotidine
    CHOP Plus Famotidine 40 mg

Primary outcome measures

  • Number of patients eith radiological and clinical improvement [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • DLBCL Lymphoma subtype --No comorbid disease

Exclusion criteria

  • Pregnancy
  • Peptic ulcer
  • Severe cardiac disease
  • Osteoporosis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Sherief Abd-Elsalam — Cairo

Publications

  • Hegazy SK, El-Haggar SM, Alhassanin SA, El-Berri EI. Comparative randomized trial evaluating the effect of proton pump inhibitor versus histamine 2 receptor antagonist as an adjuvant therapy in diffuse large B-cell lymphoma. Med Oncol. 2021 Jan 4;38(1):4. doi: 10.1007/s12032-020-01452-z. PMID 33394214

Identifiers

NCT: NCT03647072 · eman elberry

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗