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Impact of Multiple Electrolytes Injection Ⅱ and Saline on Hyperchloremia in Patients With Aneurysmal Subarachnoid Hemorrhage:a Pilot Study

Primary Purpose

Aneurysmal Subarachnoid Hemorrhage, Hyperchloremia

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
maintenance fluid
Sponsored by
Capital Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aneurysmal Subarachnoid Hemorrhage focused on measuring saline, balanced crystalloids

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with aneurysmal subarachnoid hemorrhage; Expected ICU stay > 24 hours. Exclusion Criteria: Under 18 years of age; Pregnancy; Patients at imminent risk for death within 24 hours; Patients with a known history of serious cardiovascular, respiratory, kidney, liver, blood, or immune disease; Azotemia (BUN > 200μmol/L), hypokalemia (blood potassium < 2.5mmol/L), hypocalcemia (blood calcium < 1.8mmol/L); Patients routinely receiving renal replacement therapy (RRT); Declined to participate in the study.

Sites / Locations

  • ICU, Beijing Tiantan Hospital, Capital Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

multiple electrolytes solution group

saline group

Arm Description

Experimental group drugs: Multiple Electrolytes Injection(II) Manufacturer: B.Braun Melsungen AG Dosage Form: Liquid Specification: 500ml/ bag Ingredients: Per 1000ml contains: sodium chloride 6.799g, potassium chloride 0.2984g, calcium chloride 0.3675g, magnesium chloride 0.2033g, sodium acetate 3.266g, L-malic acid 0.671, sodium hydroxide 0.200g Duration :36 months Storage conditions: airtight storage, storage temperature shall not exceed 25, can not be refrigerated or frozen

Control group drug: Sodium chloride injection Manufacturer: Hua Run Shuang He Pharmaceutical Co., LTD. Dosage Form: Liquid Specification: 500ml:4.5g Ingredients: Per 1000ml contains sodium chloride 9.0g Duration: 36 months Storage conditions: airtight storage

Outcomes

Primary Outcome Measures

Hyperchloremia
The incidence of hyperchloremia

Secondary Outcome Measures

Hyperchloremia acidosis
Incidence of hyperchloremia acidosis
AKI
Incidence of acute kidney injury
RRT
Incidence of new renal replacement therapy
hospital length of stay
hospital length of stay
hospitalization expense
money spend during this hospitalization

Full Information

First Posted
September 19, 2023
Last Updated
October 8, 2023
Sponsor
Capital Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT06076590
Brief Title
Impact of Multiple Electrolytes Injection Ⅱ and Saline on Hyperchloremia in Patients With Aneurysmal Subarachnoid Hemorrhage:a Pilot Study
Official Title
Impact of Multiple Electrolytes Injection Ⅱ and Saline on Hyperchloremia in Patients With Aneurysmal Subarachnoid Hemorrhage:a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
May 1, 2023 (Actual)
Study Completion Date
May 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Capital Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this pilot randomized trial is to compare the effect of Multiple Electrolytes Injection Ⅱand saline on the occurrence of hyperchloremia within 72h of randomization in patients with aneurysmal subarachnoid hemorrhage(aSAH). A secondary aim was to provide data for the design and power of a large-scale, multicenter, randomized controlled trial.
Detailed Description
Background: The isotonic solutions commonly used in ICUs are saline (0.9% sodium chloride) and balanced crystalloid solutions (Ringer's solution, multiple electrolytes injection, etc.). Studies have shown that the lower chloride in balanced crystalloids compared to saline may result in lower risks of hyperchloremia, acute kidney injury and poor clinical outcome in critical ill patients. As a balanced crystalloid, few evidence was found on multiple electrolytes solution II in patients with aneurysmal subarachnoid hemorrhage (aSAH). Purpose This study aimed to evaluate the security and feasibility of the study. Moreover, compare the impact of multiple electrolytes injection and saline solution on hyperchloremia in aSAH patients. Method As a pilot trial of a prospective randomized controlled study, patients with aneurysmal subarachnoid hemorrhage randomly assigned to receive saline or multiple electrolytes injection II as maintenance fluid for 3 days during ICU stay.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aneurysmal Subarachnoid Hemorrhage, Hyperchloremia
Keywords
saline, balanced crystalloids

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
multiple electrolytes solution group
Arm Type
Experimental
Arm Description
Experimental group drugs: Multiple Electrolytes Injection(II) Manufacturer: B.Braun Melsungen AG Dosage Form: Liquid Specification: 500ml/ bag Ingredients: Per 1000ml contains: sodium chloride 6.799g, potassium chloride 0.2984g, calcium chloride 0.3675g, magnesium chloride 0.2033g, sodium acetate 3.266g, L-malic acid 0.671, sodium hydroxide 0.200g Duration :36 months Storage conditions: airtight storage, storage temperature shall not exceed 25, can not be refrigerated or frozen
Arm Title
saline group
Arm Type
Active Comparator
Arm Description
Control group drug: Sodium chloride injection Manufacturer: Hua Run Shuang He Pharmaceutical Co., LTD. Dosage Form: Liquid Specification: 500ml:4.5g Ingredients: Per 1000ml contains sodium chloride 9.0g Duration: 36 months Storage conditions: airtight storage
Intervention Type
Drug
Intervention Name(s)
maintenance fluid
Intervention Description
Patients are randomized to receive ether Multiple electrolytes injection II or Normal Saline for maintenance fluid during the 72 hours after enrollment. Resuscitation fluids and fluids used for drug delivery are not limited.
Primary Outcome Measure Information:
Title
Hyperchloremia
Description
The incidence of hyperchloremia
Time Frame
At 0 hours, 24 hours, 48 hours, 72 hours after enrollment
Secondary Outcome Measure Information:
Title
Hyperchloremia acidosis
Description
Incidence of hyperchloremia acidosis
Time Frame
At 0 hours, 24 hours, 48 hours, 72 hours after enrollment
Title
AKI
Description
Incidence of acute kidney injury
Time Frame
recorded at 24 hours, 48 hours, 72 hours after enrollment
Title
RRT
Description
Incidence of new renal replacement therapy
Time Frame
recorded at 24 hours, 48 hours, 72 hours after enrollment
Title
hospital length of stay
Description
hospital length of stay
Time Frame
recorded at discharge or 28 days after enrollment
Title
hospitalization expense
Description
money spend during this hospitalization
Time Frame
recorded at discharge or 28 days after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with aneurysmal subarachnoid hemorrhage; Expected ICU stay > 24 hours. Exclusion Criteria: Under 18 years of age; Pregnancy; Patients at imminent risk for death within 24 hours; Patients with a known history of serious cardiovascular, respiratory, kidney, liver, blood, or immune disease; Azotemia (BUN > 200μmol/L), hypokalemia (blood potassium < 2.5mmol/L), hypocalcemia (blood calcium < 1.8mmol/L); Patients routinely receiving renal replacement therapy (RRT); Declined to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhou Jian-Xin, MD
Organizational Affiliation
Capital Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
ICU, Beijing Tiantan Hospital, Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100070
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Impact of Multiple Electrolytes Injection Ⅱ and Saline on Hyperchloremia in Patients With Aneurysmal Subarachnoid Hemorrhage:a Pilot Study

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