ClinicalTrials.gg
RecruitingNCT07779200Updated Oct 13, 2026

Bicarbonate HD Study

An observational study in Metabolic Acidosis and CKD on Hemodialysis Patients, sponsored by East and North Hertfordshire NHS Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by East and North Hertfordshire NHS Trust · Observational

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.
Updated Oct 13, 2026Primary completion movedStudy completion movedGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

The primary goal of this single centre observational study is to look at factors that affect serum bicarbonate levels in patients on maintenance dialysis. This will be done by collecting demographic information, relevant medical history, dialysis history, potential renal acid load from diet by recording different foods consumed over 2 days in a food diary and bicarbonate levels at 3 intervals, pre and post dialysis session 1 and pre dialysis session 2.

Bicarbonate levels are of significant interest as an indicator of metabolic acidosis in CKD dialysis patients. This study will allow us to understand the efficacy of different dialysis modalities in controlling bicarbonate levels. It will also enable us to understand the idea of individualizing dialysis for patients in terms of not using a standard concentration of dialysate for all patient undergoing dialysis in this center.

Read the detailed description

Cross sectional study

02

Conditions studied

  • Metabolic Acidosis
  • CKD on Hemodialysis Patients

Browse trials for

03

In context

Acidosis

111 studies on the registry are indexed under Acidosis; 19 are open to participants now.

This study's planned enrollment of 100 is close to the median of 100 across 30 observational studies indexed under Acidosis.

Browse Acidosis studies →

Lead sponsor

East and North Hertfordshire NHS Trust is the lead sponsor of 38 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will consist of adult patients with End Stage Renal Disease (ESRD) receiving maintenance dialysis at the study centre.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years and above.
  • Ability to give .
  • End Stage Renal Disease established on maintenance dialysis for at least 3 months.
  • Patients on dialysis 3 times a week

Exclusion criteria

Exclusion Criteria:

  • Inability to give
  • Patients with acute kidney injury
  • Patients with severe
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
100 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Change in serum bicarbonate levels in patients on haemodialysis

    Serum bicarbonate concentration measured across two dialysis sessions (HD1 and HD2) measured as Pre HD1, Post HD2 and Pre HD2.

    Time frame: 3 months

Secondary outcomes

  1. Dietary Acid Load

    Potential renal acid load

    Time frame: ~ 3 months

  2. Volume of Haemodiafiltration

    Haemodiafiltration volume delivered

    Time frame: 3 months

  3. Indicators of dialysis dose

    Pre HD1 and Post HD1 serum urea

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — To be decided after data analysis is complete

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Started May 2026 (actual). Primary completion is estimated for Nov 2026, 6 months after the start.

Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 13, 2026: primary completion Aug 2026 → Nov 2026 and completion Aug 2026 → Nov 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Jul 2, 2026
First posted
Aug 21, 2026
StartActual
May 12, 2026
Primary completionEst.
Nov 2026was Aug 2026
CompletionEst.
Nov 2026was Aug 2026
Last update
Oct 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Primary completion
Aug 2026→Nov 2026
Oct 13, 2026
Study completion
Aug 2026→Nov 2026
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    Primary completion Aug 2026→Nov 2026
    Study completion Aug 2026→Nov 2026
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07779200
Lead sponsor
East and North Hertfordshire NHS Trust
Responsible party
Sponsor
First posted
Aug 21, 2026
Start date
May 12, 2026
Primary completion
Nov 2026 (estimated)
Completion
Nov 2026 (estimated)
Last update
Oct 13, 2026

Study contacts

Enric Vilar
Contact
enric.vilar@nhs.net
01438 284230 ext. 4230
Simran Sorathia
Contact
simran.sorathia@nhs.net
01438 284230 ext. 4230

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion