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Anisodamine Critically Ill SeptIc Shock (ACIdoSIS)

Primary Purpose

Septic Shock

Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
anisodamine
Sponsored by
Jinhua Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring anisodamine, septic shock

Eligibility Criteria

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

Inclusion Criteria:

  • patients with septic shock

Inclusion criteria included patients with sepsis plus use of vasopressors. Systemic inflammatory response syndrome (SIRS) is defined as meeting at least one of the following 3 criteria for a systemic inflammatory response. One of the SIRS criteria must be either the WBC criteria (a) or the body temperature criteria (b):

  1. White blood cell count >12,000 or <4,000 or >10% band forms
  2. Body temperature >38oC (any route) or <36oC (accepting core temperatures only; indwelling catheter, esophageal, rectal)
  3. Heart rate (> 90 beats/min) or receiving medications that slow heart rate or paced rhythm.

Suspected or documented infection included the following sites: thorax, urinary tract, abdomen, skin, sinuses, central venous catheters, and bacterial meningitis.

Septic shock was defined as sustained arterial hypotension with systolic blood pressure (SBP) < 90 mm Hg, mean arterial pressure (MAP) < 70 mm Hg, or an SBP decrease > 40 mm Hg, despite adequate fluid resuscitation. To ease clinical screening process, we defined septic shock as the requirement of vasopressors despite adequate fluid resuscitation. Vasopressors include norepinephrine, epinephrine, phenylephrine and dopamine>5mcg/kg/min.

Patients with following conditions will be excluded:

  1. Age<15 years old
  2. Moribund (expected to die within 24 hours)
  3. Stay in ICU for more than 24 hours
  4. Contraindications to anisodamine: elevated intracranial pressure, acute phase of intracranial hemorrhage, glaucoma, untreated bowel obstruction (surgically treated obstruction is not contraindicated), enlargement of prostate without urinary catheterization.

Sites / Locations

  • Huizhou first hospital
  • Union Hospital, Tongji medical collegue, Huazhong university of Science and Technology
  • the First Affiliated Hospital of Nanjing Medical University
  • affiliated hospital, Jiangsu University
  • Binzhou People's hospital of Shandong province
  • department of critical care medicine, Ren Ji Hospital, School of medicine, Shanghai Jiao Tong University
  • Peace hospital of Changzhi medical college
  • Zhejiang Hospital
  • Sir Run Run Shaw hospital
  • Sir Run Run Shaw hospital
  • Jinhua Municipal Central Hospital
  • Department of critical care medicine, The central hospital of Lishui City
  • Beilun People's hospital; The first affiliated hospital of Zhejiang university (Beilun Branch)
  • Taizhou hospital of Zhejiang province
  • The first People's hospital of Yongkang

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

anisodamine group

control group

Arm Description

administration of the drug

these arm do not use anisodamine, other resuscitation protocol is as usual.

Outcomes

Primary Outcome Measures

hospital mortality
the outcome will be assessed by using proportion of patients died, and relative risk will be reported.

Secondary Outcome Measures

lactate levels
the value was measured in mmol/l, and they will be compared between both arms.

Full Information

First Posted
April 30, 2015
Last Updated
September 23, 2021
Sponsor
Jinhua Central Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02442440
Brief Title
Anisodamine Critically Ill SeptIc Shock
Acronym
ACIdoSIS
Official Title
Effectiveness of Anisodamine for the Treatment of Critically Ill Patients With Septic Shock: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
October 2020 (Actual)
Study Completion Date
October 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jinhua Central Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Anisodamine has been widely used in China for its pharmacological effect on improving microcirculation during shock. It has been reported that anisodamine is effective in reducing mortality rate in children with meningitis. however, its effectiveness in patients with septic shock has not been systematically investigated. The aim of the study is to investigate the effectiveness of anisodamine in the treatment of patients with septic shock.
Detailed Description
Septic shock is an important contributor of mortality in the intensive care unit (ICU). The crude mortality is reported to be from 30% to 65% (1-5). Although there are significant advances in the management of septic shock in recent decades, the mortality rate was only marginally reduced. For example, the CUB-Réa Network study reported that the mortality rate of septic shock declined from 62.1% in 1993 to 55.9% in 2000 (6). The well-known Surviving Sepsis Campaign has also made every effort to reduce mortality rate of severe sepsis and septic shock. The organization recommended bundled strategies including early goal directed therapy (EGDT) for the management of septic shock (7,8). Although EGDT was once the mainstay therapy of septic shock, its efficacy has been questioned by recent several large randomized controlled trials (9,10). Therefore, the treatment of septic shock is still a global challenge and there is no well-established intervention that can reduce its mortality. Anisodamine is an active agent isolated from a Chinese herb medicine. Both experimental and clinical studies have shown some potential beneficial effects of anisodamine in improving outcomes of shock (11-13). It was reported that anisodamine could reduce the mortality rate of fulminant epidemic meningitis from 66.9% to 12.4% (14). The efficacy of anisodamine might be mediated via the inhibition of thromboxane synthesis, granulocyte and platelet aggregation (15). Although anisodamine has been widely used in the treatment of septic shock in mainland China, there is no solid evidence from well designed clinical trials to support its efficacy. The aim of the study is to investigate the effectiveness of anisodamine in the treatment of critically ill patients with septic shock.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
anisodamine, septic shock

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
355 (Actual)

8. Arms, Groups, and Interventions

Arm Title
anisodamine group
Arm Type
Experimental
Arm Description
administration of the drug
Arm Title
control group
Arm Type
No Intervention
Arm Description
these arm do not use anisodamine, other resuscitation protocol is as usual.
Intervention Type
Drug
Intervention Name(s)
anisodamine
Other Intervention Name(s)
654-2
Intervention Description
Anisodamine will be given first as bolus of 10 mg, followed by 0.1-0.5mg/kg/hr. The adjustment of pump infusion rate is largely at the discretion of treating physician, with the aim of improving microcirculation and limit the side effect to a minimum. For example, if serum lactate continues to elevate, the infusion rate can be increased. Discontinuation on severe side effect or recovery of shock (normalized lactate, weaned from vasopressor) or death.
Primary Outcome Measure Information:
Title
hospital mortality
Description
the outcome will be assessed by using proportion of patients died, and relative risk will be reported.
Time Frame
from ICU admission to hospital discharge (participants will be followed for the duration of hospital stay, an expected average of 28 days)
Secondary Outcome Measure Information:
Title
lactate levels
Description
the value was measured in mmol/l, and they will be compared between both arms.
Time Frame
from ICU admission to hospital discharge (participants will be followed for the duration of hospital stay, an expected average of 28 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with septic shock Inclusion criteria included patients with sepsis plus use of vasopressors. Systemic inflammatory response syndrome (SIRS) is defined as meeting at least one of the following 3 criteria for a systemic inflammatory response. One of the SIRS criteria must be either the WBC criteria (a) or the body temperature criteria (b): White blood cell count >12,000 or <4,000 or >10% band forms Body temperature >38oC (any route) or <36oC (accepting core temperatures only; indwelling catheter, esophageal, rectal) Heart rate (> 90 beats/min) or receiving medications that slow heart rate or paced rhythm. Suspected or documented infection included the following sites: thorax, urinary tract, abdomen, skin, sinuses, central venous catheters, and bacterial meningitis. Septic shock was defined as sustained arterial hypotension with systolic blood pressure (SBP) < 90 mm Hg, mean arterial pressure (MAP) < 70 mm Hg, or an SBP decrease > 40 mm Hg, despite adequate fluid resuscitation. To ease clinical screening process, we defined septic shock as the requirement of vasopressors despite adequate fluid resuscitation. Vasopressors include norepinephrine, epinephrine, phenylephrine and dopamine>5mcg/kg/min. Patients with following conditions will be excluded: Age<15 years old Moribund (expected to die within 24 hours) Stay in ICU for more than 24 hours Contraindications to anisodamine: elevated intracranial pressure, acute phase of intracranial hemorrhage, glaucoma, untreated bowel obstruction (surgically treated obstruction is not contraindicated), enlargement of prostate without urinary catheterization.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
kun chen, MSc
Organizational Affiliation
Jinhua Municipal Central Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Huizhou first hospital
City
Huizhou
State/Province
Guangdong
ZIP/Postal Code
516000
Country
China
Facility Name
Union Hospital, Tongji medical collegue, Huazhong university of Science and Technology
City
Wuhan
State/Province
Hubei
Country
China
Facility Name
the First Affiliated Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Facility Name
affiliated hospital, Jiangsu University
City
Zhenjiang
State/Province
Jiangsu
Country
China
Facility Name
Binzhou People's hospital of Shandong province
City
Binzhou
State/Province
Shandong
Country
China
Facility Name
department of critical care medicine, Ren Ji Hospital, School of medicine, Shanghai Jiao Tong University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200001
Country
China
Facility Name
Peace hospital of Changzhi medical college
City
Changzhi
State/Province
Shanxi
Country
China
Facility Name
Zhejiang Hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China
Facility Name
Sir Run Run Shaw hospital
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
321000
Country
China
Facility Name
Sir Run Run Shaw hospital
City
Hangzhou
State/Province
Zhejiang
Country
China
Facility Name
Jinhua Municipal Central Hospital
City
Jinhua
State/Province
Zhejiang
ZIP/Postal Code
321000
Country
China
Facility Name
Department of critical care medicine, The central hospital of Lishui City
City
Lishui
State/Province
Zhejiang
ZIP/Postal Code
323000
Country
China
Facility Name
Beilun People's hospital; The first affiliated hospital of Zhejiang university (Beilun Branch)
City
Ningbo
State/Province
Zhejiang
Country
China
Facility Name
Taizhou hospital of Zhejiang province
City
Taizhou
State/Province
Zhejiang
ZIP/Postal Code
317000
Country
China
Facility Name
The first People's hospital of Yongkang
City
Yongkang
State/Province
Zhejiang
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
34579741
Citation
Yu Y, Zhu C, Hong Y, Chen L, Huang Z, Zhou J, Tian X, Liu D, Ren B, Zhang C, Hu C, Wang X, Yin R, Gao Y, Zhang Z. Effectiveness of anisodamine for the treatment of critically ill patients with septic shock: a multicentre randomized controlled trial. Crit Care. 2021 Sep 27;25(1):349. doi: 10.1186/s13054-021-03774-4.
Results Reference
derived
PubMed Identifier
28203424
Citation
Zheng Y, Li Y, Liu X, Zhang R, Wang Z, Sun H, Liu S. A phase III, multicenter randomized controlled trial of neo-adjuvant chemotherapy paclitaxel plus cisplatin versus surgery alone for stage IIA-IIIB esophageal squamous cell carcinoma. J Thorac Dis. 2017 Jan;9(1):200-204. doi: 10.21037/jtd.2017.01.44.
Results Reference
derived
PubMed Identifier
26605292
Citation
Zhang Z, Zhou J, Shang Y, Wang X, Yin R, Zhu Z, Chen W, Tian X, Yu Y, Zuo X, Chen K, Ji X, Ni H; Anisodamine Critically Ill SeptIc Shock (ACIdoSIS) study group. Effectiveness of anisodamine for the treatment of critically ill patients with septic shock (ACIdoSIS study): study protocol for randomized controlled trial. Ann Transl Med. 2015 Oct;3(17):246. doi: 10.3978/j.issn.2305-5839.2015.10.03.
Results Reference
derived

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Anisodamine Critically Ill SeptIc Shock

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