Clinical Trials Logo

Clinical Trial Summary

Coffee is the most consumed drink worldwide, sometimes needed to boost energy and other times to entertain social connectivity. Caffeine is mostly present unbound in the plasma, only 10 to 30% of caffeine binds to plasma proteins. It is distributed freely into the intracellular space, and it has a small distribution volume. Therefore, caffeine can pass through the dialysis membrane during a standard hemodialysis session. In hemodialysis patients, headache occurs in 40 to 75% of patients. Some authors have suggested that one of the reasons of headache during hemodialysis is caffeine withdrawal. This trial aims to find whether coffee intake during hemodialysis reduces the headache episodes. It is a randomized double blind multicenter trial where 160 patients will be randomized to 2 groups: group 1 of 80 patients will be given a cup of coffee each dialysis session for 4 weeks and group 2 will receive decaffeinated coffee each dialysis session for 4 weeks.


Clinical Trial Description

Coffee is the most consumed drink worldwide, sometimes needed to boost energy and other times to entertain social connectivity. It is known also to cause addiction and thus be a cause for withdrawal symptoms such as headache and irritability. Coffee is not contra-indicated in patients with chronic kidney disease. Caffeine is mostly present unbound in the plasma, only 10 to 30% of caffeine binds to plasma proteins. It is distributed freely into the intracellular space, and it has a small distribution volume within the body around 0,7L/kg. Therefore, caffeine can pass through the dialysis membrane during a standard hemodialysis session. In hemodialysis patients, intra-dialytic hypotension, fatigue post-dialysis and headache occur in 40 to 75% of patients. Some authors have suggested that one of the reasons of headache during hemodialysis is caffeine withdrawal.

This trial aims to find out whether coffee consumption during dialysis could decrease headache episodes.

Methods

Study setting All patients on chronic hemodialysis in three Lebanese dialysis units, Saint-Georges Ajaltoun hospital, Hôtel-Dieu de France and Bellevue Medical Center will be included.

Trial design and participants This is a randomized, controlled, double-blind, multi-center clinical trial. Patients will be randomized to one of two arms and then group one will receive the coffee during hemodialysis session and group two will receive decaffeinated coffee.

Blinding will be ensured by designating an external employee that will hold the cups of coffee to the unit's nurses every day with the name of each patient on the cup.

Randomization Patients will be assigned to receive coffee during hemodialysis or not using a 1:1 allocation ratio.

Interventions Patients will be randomly assigned to one of two groups: Group 1 will receive a cup of coffee (80 cc) in the middle of the dialysis session every session for 4 weeks. Group 2 will receive non-caffeinated cup of coffee (80 cc) in the middle of the dialysis session every session for 4 weeks. The coffee that will be used is the boiled unfiltered Arabica coffee with a ratio of water to coffee of 800 ml/125 g. Patients can add sugar to their coffee if they want. Ultrafiltration rate will not exceed 13 mL//kg/hour for all included patients.

Participant timeline Every patient will be followed from first day of randomization till the end of the month (4 weeks follow-up).

Sample size calculation If we consider a two-sided alpha of 5% and power of 90% and a prevalence of headache in the dialysis population up to 75% that will be reduced by 25% in the group taking caffeine, the total sample size needed would be 160 patients, 80 in each arm.

Data collection

Variables that will be collected include:

- Personal information: age, sex, smoking, alcohol intake per week, hypertension (at least one antihypertensive drug)

- Caffeine intake: number of coffee cups at home per day (outside the dialysis session), coffee intake before the dialysis session (yes/no), coffee intake during the dialysis session (yes/no)

- Medical history: diabetes, hypertension, coronary artery disease, history of headache or migraine

- Medications: beta blockers, antidepressants, benzodiazepine

- Dialysis sessions related information: dialysis vintage (months), urea reduction ratio (URR) of the month

- Clinical variables: number of intra-dialytic hypotensive the month before the trial and during the trial, number of intra-dialytic and home headache episodes during the trial, pre-dialysis systolic and diastolic blood pressure and heart rate of the first and the last session of the trial, insomnia before and at the end of the trial, energy after a dialysis session before and after the trial and irritability before and after the trial.

- Adverse events will be also reported such as arrhythmia, tachycardia or hypertension.

Statistical analysis Continuous variables will be presented as mean ± standard deviation (SD) and categorical variables as percentages. The effectiveness of the randomization will be checked by comparing baseline variables with the appropriate tests.

The analysis will depend on the distribution of the outcome variables:

If outcome variables are normally or quasi-normally distributed, Hotelling's T-Squared will be used as an overall multivariate test for the difference between the 2 groups, followed by t-tests to assess individual outcomes.

If outcome variables are skewed, the Mann-Whitney test will be used. Bonferroni correction will be used to adjust for multiple comparisons. A P-value of ≤0.05 is considered statistically significant.

Definitions Hypotensive episodes are defined as drop of systolic blood pressure below 90 mmHg or of 20 mmHg accompanied with clinical symptoms such as muscle cramps, chest pain, dyspnea, dizziness, headache, abdominal pain, nausea, vomiting, weakness, anxiety, paleness and sweating. Hypotensive episodes during dialysis usually occur in 15-30% of cases.

Irritability and energy will be assessed based on two questions:

- Have you been a very nervous person, irritated by minor incidents? (yes/no)

- How much energy do you feel after your dialysis session on a scale from 1 to 10?

Insomnia will be assessed by two questions: have you any difficulty sleeping at night? (yes/no), how many hours do you sleep at night?

Ethical approval The study will get approval from the ethics committee of Saint-Joseph University and is in agreement with the Helsinki Declaration of 1975. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04057313
Study type Interventional
Source Saint-Joseph University
Contact
Status Completed
Phase N/A
Start date September 1, 2019
Completion date October 1, 2019

See also
  Status Clinical Trial Phase
Completed NCT05980845 - The Effect Nature Sounds and Music on Hemodialysis Patients N/A
Recruiting NCT05020717 - Retrospective Survey of Hyperkalemia in Hemodialysis
Recruiting NCT04046042 - Virtual Reality Intradialysis: Last vs. First Part of the Session N/A
Recruiting NCT04094038 - The Effect of Intradialytic Parenteral Nutrition on Nutritional Status and Quality of Life in Hemodialysis Patients Phase 4
Completed NCT03311581 - The Feasibility of Propofol TCI in Hemodialysis Patients Undergoing Arteriovenous Shunt Surgery Phase 1
Completed NCT05531175 - REIKI APPLICATION PAIN, FATIGUE AND ITCHING IN HEMODIALYSIS PATIENTS N/A
Completed NCT03061552 - Inferior Vena Cava Sonography in Hemodialysis Patients and Quality of Life N/A
Completed NCT03251573 - The Cohort Study of Cognitive Impairment in Chinese Hemodialysis Patients
Completed NCT03527680 - Effect of Lactobacillus Rhamnosus on Serum Uremic Toxins in Hemodialysis N/A
Completed NCT05568342 - The Effect of Roy Adaptation-Based Nursing Intervention N/A
Completed NCT04063423 - Non- Clinical Coagulation Activation During Hemodialysis
Active, not recruiting NCT06203795 - Dialysis Performance of the FX CorAL Membrane N/A
Recruiting NCT04319328 - Is Cefazolin, Ceftazidime and Ciprofloxacin Dosing Optimal in Hemodialysis Patients?
Completed NCT03627884 - Outcomes of the Use of Sodium Bicarbonate (8.4%) Solution as a Catheter Lock Solution to Prevent Hemodialysis Catheter Loss Due to Lumen Clot Formation Phase 4
Completed NCT05132036 - Lung Ultrasound Assessment of Fluid Overload in Haemodialysis Patients N/A
Completed NCT03076528 - An Innovative Virtually Supervised Exercise for Dialysis Patients Phase 2
Recruiting NCT06098443 - Acupressure Versus Transcutaneous Electrical Nerve Stimulation on Pain and Quality of Life Intradialysis N/A
Not yet recruiting NCT05534542 - Comparıson of the effectıveness of ıntradıalıtıc Core stabılızatıon and aerobıc exercıse ın hemodıalysıs patıents N/A
Completed NCT04645121 - Carbon Monoxide-based Rebreathing Method and Bioimpedance in Hemodialysis Patients
Recruiting NCT04127877 - Bio Impedance-assisted Monitoring of Chronic Hemodialysis Patients N/A