Effect of Proton Pump Inhibitor of Daily Use for One Month on Kidney Function Test
1 other identifier
interventional
200
0 countries
N/A
Brief Summary
The aim of this study to: evaluate the association between prolonged use of PPI and adverse renal outcomes on patients with normal renal function and others with abnormal renal function
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Nov 2019
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 3, 2019
CompletedFirst Posted
Study publicly available on registry
July 17, 2019
CompletedStudy Start
First participant enrolled
November 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2021
CompletedJuly 17, 2019
July 1, 2019
1 year
July 3, 2019
July 15, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
kidney function
eGFR=175xage(y/0)x\^(-0.203)xplasma creatinine (mg/dl)x\^(-1.154)
one month
Study Arms (2)
pantoprazole with normal kidney function
EXPERIMENTALuse pantoprazole for one month and after one month i will do for them kidney functions test
pantoprazole with abnormal kidney function
EXPERIMENTALuse pantoprazole for one month and after one month i will do for them kidney functions test
Interventions
effect of this drug on renal function
Eligibility Criteria
You may qualify if:
- patients with peptic ulcer disease or gastroesophagial reflux with normal l renal function
- patients with peptic ulcer disease or gastroeosophagial reflux with abnormal renal function
You may not qualify if:
- cigarette smoker: Cigarette smoking status was defined categorically as current,former, or never smoker at baseline.
- biabetic patients: diabetes mellitus is defined by a fasting blood glucose concentration \>\_ 126 mg/dl ,random glucose level of \>200 mg 3-patients take corticosteroid 4-patients with hypersensitivity to these drugs
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Lecturer
Study Record Dates
First Submitted
July 3, 2019
First Posted
July 17, 2019
Study Start
November 1, 2019
Primary Completion
November 1, 2020
Study Completion
December 1, 2021
Last Updated
July 17, 2019
Record last verified: 2019-07