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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03806088
Other study ID # IslamiaUS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 1, 2018
Est. completion date November 25, 2019

Study information

Verified date November 2019
Source Islamia University of Bahawalpur
Contact H M Attaullah, pharm.D
Phone 03044229043
Email attaullah@inbox.eu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

an observational cross-sectional study is done to calculate the electrolyte imbalance at different stages of chronic kidney disease at tertiary care hospital.


Description:

an observational cross-sectional study is done to calculate the electrolyte imbalance at different stages of chronic kidney disease at tertiary care hospitals of south Punjab, Pakistan .The outcomes of chronic kidney disease and end stage of renal failure will be calculated according to standard protocol. Under the supervision of pathologists, pharmacologists, pharmacists, nephrologists, urologists and biostatistician. The standard protocol was authorized by ethical committee of each center. patient consent form was


Recruitment information / eligibility

Status Recruiting
Enrollment 385
Est. completion date November 25, 2019
Est. primary completion date November 25, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- CKD patients ranging

- age from 20-80

- dialysis and pre-dialysis patients

- who provide written consent form

Exclusion Criteria:

- congenital one kidney patients

- organ or kidney donors and transplantation

- pregnant women

- renal injury during trauma

Study Design


Locations

Country Name City State
Pakistan Faculty of Pharmacy and Alternative Medicine Khawaja Freed Campus Bahawalpur Punjab

Sponsors (1)

Lead Sponsor Collaborator
Islamia University of Bahawalpur

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum potassium in mEq/L Serum potassium in mEq/L by taking blood sample under standard condition 2days
Primary serum urea in mg/dl serum urea in mg/dl by taking blood sample under standard condition 2days
Primary Serum creatinine in mg/dl Serum creatinine in mg/dl by taking blood sample under standard condition 2days
Primary Serum calcium in mg/dl Serum calcium in mg/dl by taking blood sample under standard condition 2days
Primary Serum sodium in mEq/L Serum sodium in mEq/L by taking blood sample under standard condition 2days
Secondary Blood pressure in mm of Hg Blood pressure in mm of Hg 2days
Secondary Blood glucose concentration in mg/dl Blood glucose concentration in mg/dl random 2days
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