- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05090020
Hypernatremia in Hydatid Cyst Treatment
October 10, 2021 updated by: Aydın Aktaş, Trabzon Kanuni Education and Research Hospital
Systematic Review of Hypernatremia Following Hydatid Cyst Treatment
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.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aydıin Aktas
- Phone Number: +905308807983
- Email: aydinaktas2004@gmail.com
Study Contact Backup
- Name: Cuneyt Kayaalp
- Email: cuneytkayaalp@hotmail.com
Study Locations
-
-
Ortahisar
-
Trabzon, Ortahisar, Turkey
- Recruiting
- Aydıin Aktas
-
Contact:
- Aydıin Aktas
- Phone Number: 05308807983
- Email: aydinaktas2004@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
7 years to 90 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients treated who hydatid cyst with hypertonic saline
Description
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.
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Hypernatremia
Hypernatremia (plasma sodium value above 145 mmol/L) due to HS use in the treatment of hydatid cyst.
|
Surgery and PAIR
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevention of hypernatreima
Time Frame: 3 month
|
Hypernatremia is plasma sodium value above 145 mmol/L.
|
3 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Aydin Aktas, Kanuni Training and Research Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2021
Primary Completion (Anticipated)
October 15, 2021
Study Completion (Anticipated)
October 31, 2021
Study Registration Dates
First Submitted
September 26, 2021
First Submitted That Met QC Criteria
October 10, 2021
First Posted (Actual)
October 22, 2021
Study Record Updates
Last Update Posted (Actual)
October 22, 2021
Last Update Submitted That Met QC Criteria
October 10, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TrabzonKERH
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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