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Hemodialysis ComplicationCoffeeHDNCT04057313

Coffee in Hemodialysis and Headache

A study testing Coffee in people with Hemodialysis Complication, run by Saint-Joseph University at 1 site in Lebanon.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Hemodialysis Complication
What is being tested?
Coffee
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
156 participants
Where
1 siteLebanon
Study dates
1 Sep 2019to 1 Oct 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • All adult patients > 18 years old on chronic hemodialysis

Who cannot join

  • patients with a history of chronic or paroxysmal atrial fibrillation
  • patients on chronic systematic pain killers
  • patients with a problem of swallowing food or drinks
  • patients who are coffee allergic or intolerant.

Trial locations and contacts

1 site in 1 country.

Lebanon1 site
  • Saint-Georges Hospital

    Ajaltoun, Kesrouan

Other trials in Lebanon

About this study

Official title: Coffee Intake in HemoDialysis and Headache (CoffeeHD): a Randomized Double Blind Multicenter Clinical Trial

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.

Read the detailed 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.

Being tested
Coffee
Keywords
Coffee, Headache, Intra-dialytic hypotension
Medical subject headings
Headache

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CoffeeDietary supplement

    Coffee used will be the boiled unfiltered Arabica coffee

Study groups in NCT04057313
Study groupRoleWhat they receive
Group 1Active comparatorGroup 1 will receive 80 cc of coffee in the dialysis session
Receives: Dietary Supplement: Coffee
Group 2Placebo comparatorGroup 2 will receive 80 cc of decaffeinated coffee in the dialysis session
Receives: Dietary Supplement: Coffee

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. number of headache episodes

    number of headache episodes during or immediately after dialysis over 12

    Measured: 4 weeks

Secondary outcomes (4)
  1. number of intra-dialytic hypotensive episodes

    number of intra-dialytic hypotensive episodes during trial over 12

    Measured: 4 weeks

  2. number of sleeping hours per night

    number of sleeping hours per night during the trial (average)

    Measured: 4 weeks

  3. energy after dialysis

    energy after dialysis on a scale from 1 to 10 (1 is no energy and 10 is full energy)

    Measured: 4 weeks

  4. irritability

    irritability during the trial (question: are you easily irritated? yes/no)

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2019
  2. Study start1 Sep 2019
  3. Primary completion1 Oct 2019
  4. Study completion1 Oct 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
A randomized multicenter trial: hemodialysis patients in three dialysis units will be randomized to two groups, group 1 will take coffee for 4 weeks, group 2 will take decaffeinated coffee for 4 weeks
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
156 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04057313
Sponsor's protocol ID
CoffeeHD2019
Acronym
CoffeeHD
Status last verified
Oct 2020
First submitted
11 Aug 2019
Last updated
14 Oct 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Aoun MH, Hilal N, Beaini C, Sleilaty G, Hajal J, Boueri C, Chelala D. Effects of Caffeinated and Decaffeinated Coffee on Hemodialysis-Related Headache (CoffeeHD): A Randomized Multicenter Clinical Trial. J Ren Nutr. 2021 Nov;31(6):648-660. doi: 10.1053/j.jrn.2021.01.025. Epub 2021 Mar 12.

    PubMed 33715955

Questions about this trial

What is this clinical trial studying?

A study testing Coffee in people with Hemodialysis Complication, run by Saint-Joseph University at 1 site in Lebanon.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Lebanon. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

number of headache episodes (time frame: 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04057313, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2020.

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