ClinicalTrials.gg
Status unknownNCT05090020Updated Oct 22, 2021

Hypernatremia in Hydatid Cyst Treatment

An observational study in Echinococcosis, Hepatic, sponsored by Trabzon Kanuni Education and Research Hospital. Status unknown at 1 site in Turkey. Open to participants aged 7 Years to 90 Years. Per ClinicalTrials.gov, last updated 2021-10-22.

Sponsored by Trabzon Kanuni Education and Research Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
30
Ages
7 Years to 90 Years
Sex
All
01

Study summary

Hypertonic saline (HS) is one of the most widely used scolocidal agents in the treatment of hydatid cysts. Hypernatremia is one of the complications associated with the use of HS. It can cause hypernatremia, acid-base disorder, impaired lung, renal, cardiac and neurological functions and even death. Therefore, caution should be exercised in the use of HS, and open technique should be preferred in surgery.

02

Conditions studied

  • Echinococcosis, Hepatic

Keywords

  • Echinococcosis
  • Hepatic
  • hypernatremia
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In context

Echinococcosis

25 studies on the registry are indexed under Echinococcosis; 4 are open to participants now.

This study's planned enrollment of 30 is below the median of 45 across 18 observational studies indexed under Echinococcosis.

Browse Echinococcosis studies →

Lead sponsor

Trabzon Kanuni Education and Research Hospital is the lead sponsor of 12 studies on the registry; 4 are open to participants now.

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

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Who can participate

Ages eligible
7 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients treated who hydatid cyst with hypertonic saline

Eligibility criteria

Inclusion Criteria: Patients who developed hypernatremia (plasma sodium value above 145 mmol/L) due to HS use in the treatment of hydatid cyst were included to study -

Exclusion Criteria:Patients who developed hypernatremia due to other treatments were excluded from the study.

-

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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Hypernatremia

    Hypernatremia (plasma sodium value above 145 mmol/L) due to HS use in the treatment of hydatid cyst.

    Procedure: Treatment

Interventions

  • ProcedureTreatment

    Surgery and PAIR

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What researchers measure

Primary outcomes

  1. Prevention of hypernatreima

    Hypernatremia is plasma sodium value above 145 mmol/L.

    Time frame: 3 month

07

Study locations

1 of 1 sites recruiting
  • Aydıin Aktas
    Trabzon, Ortahisar, Turkey
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Feb 2021 (actual). Primary completion is estimated for Oct 2021, 8 months after the start.

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

Registered
Sep 26, 2021
First posted
Oct 22, 2021
StartActual
Feb 1, 2021
Primary completionEst.
Oct 15, 2021
CompletionEst.
Oct 31, 2021
Last update
Oct 22, 2021
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.
No changes since tracking began. The registry record was last updated on Oct 22, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05090020
Lead sponsor
Trabzon Kanuni Education and Research Hospital
Responsible party
Aydın Aktaş (Associate Professor Doctor, Trabzon Kanuni Education and Research Hospital) — Principal investigator
First posted
Oct 22, 2021
Start date
Feb 1, 2021
Primary completion
Oct 15, 2021 (estimated)
Completion
Oct 31, 2021 (estimated)
Last update
Oct 22, 2021

Study contacts

Aydıin Aktas
Contact
aydinaktas2004@gmail.com
+905308807983
Cuneyt Kayaalp
Contact
cuneytkayaalp@hotmail.com
Aydin Aktas
study chair · Kanuni Training and Research Hospital

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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