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Comparison of CLSB With Sedation Versus General Endotracheal Anesthesia on Postoperative Outcomes in Elderly Patients Undergoing Hip Fracture Surgery

Primary Purpose

Anesthesia Morbidity, Anesthesia; Adverse Effect

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
anesthesia
Sponsored by
Shanghai 6th People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anesthesia Morbidity focused on measuring general anesthesia, sacral plexus block, lumbar plexus block, hip fracture, elderly

Eligibility Criteria

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

Inclusion Criteria:

  1. Age ≥77 years old;
  2. First unilateral surgery for hip fracture including femoral neck, intertrochanteric or subtrochanteric fracture;
  3. Patient with planned hip fracture surgery within 24-72 h;
  4. Patient without peripheral nerve block within 24 h prior to surgery;
  5. The ability to receive written informed consent from the patient or patient's legal representative.

Exclusion Criteria:

  1. Refuse to participate;
  2. Unable to perform nerve block;
  3. Multiple trauma, multiple fractures or other fractures outside the inclusion criteria, such as pathological fractures, pelvic fractures, femur fractures;
  4. Prosthetic fracture;
  5. Scheduled for bilateral hip fracture surgery;
  6. Usage of bone-cement fixation in the surgery;
  7. With recent cerebral stroke (<3 months);
  8. Combined with active heart disease (unstable angina, acute myocardial infarction, recent myocardial infarction; decompensated heart failure; symptomatic arrhythmia; severe mitral or aortic stenotic heart disease);
  9. Patient with known severe lung and/or airway disease, acute respiratory failure, acute pulmonary infection, and acute attack of bronchial asthma;
  10. Current enrolment in another clinical trial;
  11. Contraindication for general endotracheal anesthesia(drug allergies to general anesthesia, difficult airway);
  12. Contraindication for lumbar and sacral plexus block(infection at the site of needle insertion, coagulopathy, allergy to local anesthetics).

Sites / Locations

  • Shanghai Sixth People's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

GA group

CLSB group

Arm Description

general anesthesia(GA) group: Open peripheral vein fluid infusion, radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring Propofol (1.5-3mg/kg), cis-atracurium(0.1-0.15mg/kg) and sulfentanyl(0.2-0.6μg/kg) anesthesia-induced intubation, mechanical ventilation to maintain normal PETCO2 Use sevoflurane, propofol and sulfentanyl to maintain anesthesia, and add cis-atracurium as needed Transfer to ICU after surgery

combined lumbar plexus and sacral plexus block(CLSB) group: Open peripheral vein fluid infusion In lateral position (affected side upward), ultrasound-guided lumbar plexus block (0.375% ropivacaine, Lumbar 2-3 or/and 3-4vertebral space level, 25ml), then sacral plexus block (0.375% ropivacaine, 20ml) Radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring, and blockade effectiveness was evaluated 30min after nerve block After reaching satisfactory blockade, target-controlled infusion of propofol was used to maintain Ramsay sedation score between 5-6 points, monitoring PETCO2 through nasopharyngeal airway, maintain autonomous respiration, and add small-dose fentanyl (10-20μg/time) as needed Transfer to ICU after surgery

Outcomes

Primary Outcome Measures

mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.

Secondary Outcome Measures

Duration of surgery
The time spent on the surgery will be recorded.
Intraoperative complications
Intraoperative hypotension and vasopressor dosage Intraoperative arrhythmia, myocardial ischemia, myocardial infarction, massive hemorrhage, pulmonary embolism and hypoxemia Intraoperative blood loss and blood transfusion volume
Incidence of various complications and comprehensive complication index during hospitalization after surgery
SOFA score(sequential organ failure assessment score)
Sepsis-related organ failure assessment score, also known as sequential organ failure assessment score (SOFA score), is used to track a person's status during the stay in an intensive care unit (ICU) to determine the extent of a person's organ function or rate of failure. The score is based on six different scores, one each for the respiratory, cardiovascular, hepatic, coagulation, renal and neurological systems.Both the mean and highest SOFA scores are predictors of outcome. An increase in SOFA score during the first 24 to 48 hours in the ICU predicts a mortality rate of at least 50% up to 95%. Scores less than 9 give predictive mortality at 33% while above 11 can be close to or above 95%.
Length of stay in ICU and hospital
the Confusion Assessment Method(CAM)
The Confusion Assessment Method includes an instrument and diagnostic algorithm for identification of delirium.The CAM instrument assesses the presence, severity, and fluctuation of 9 delirium features:acute onset, inattention, disorganized thinking, altered level of consciousness, disorientation, memory impairment, perceptual disturbances, psychomotor agitation or retardation, and altered sleep-wake cycle.
MMSE(Mini-mental State Examination)
The Mini-Mental State Examination (MMSE) or Folstein test is a 30-point questionnaire that is used extensively in clinical and research settings to measure cognitive impairment. It is commonly used in medicine and allied health to screen for dementia. It is also used to estimate the severity and progression of cognitive impairment and to follow the course of cognitive changes in an individual over time; thus making it an effective way to document an individual's response to treatment. The MMSE test includes simple questions and problems in a number of areas: the time and place of the test, repeating lists of words, arithmetic such as the serial sevens, language use and comprehension, and basic motor skills.
High-sensitivity cardiac troponin T(hs-cTnT)
Cardiac troponin is the preferred biomarker for the diagnosis of acute myocardial infarction. A high-sensitivity cardiac troponin T(hs-cTnT) assay permits detection of very low levels of cTnT.

Full Information

First Posted
October 15, 2017
Last Updated
August 25, 2022
Sponsor
Shanghai 6th People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03318133
Brief Title
Comparison of CLSB With Sedation Versus General Endotracheal Anesthesia on Postoperative Outcomes in Elderly Patients Undergoing Hip Fracture Surgery
Official Title
Comparison of Combined Lumbar and Sacral Plexus Block With Sedation Versus General Endotracheal Anesthesia on Postoperative Outcomes in Elderly Patients Undergoing Hip Fracture Surgery(CLSB-HIPELD): Rationale and Design of a Prospective, Multicenter, Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 4, 2018 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai 6th People's Hospital

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
Hip fracture is a global public health problem. The postoperative mortality and disability rate of hip fracture is high, and early surgery is still the most effective treatment method, but these patients are often associated with concurrent heart and lung and other organ dysfunction, anesthesia and surgery are extremely risky, mainly associated with high incidence of complications in the pulmonary and cardiovascular system, and anesthesia plays a vital role in ensuring that these patients can safely and effectively get through the perioperative period. The research on the relationship between anesthetic methods and hip fracture surgery prognosis mainly focuses on comparison between neuraxial anesthesia (including spinal anesthesia and epidural anesthesia) and general anesthesia with endotracheal intubation until now. In addition to general anesthesia with endotracheal intubation and neuraxial anesthesia, ultrasound-guided lumbar plexus and sciatic nerve block has been widely used in hip fracture surgery in recent years, especially for some high-risk patients with cardiopulmonary dysfunction. However, it is not clear whether ultrasound-guided combined lumbar plexus and sacral plexus block with sedative anesthesia can improve the prognosis of elderly patients with hip fracture, and in this study, we plan to make a prospective, multicenter, randomized controlled clinical trial to compare the effects of general anesthesia with endotracheal intubation and ultrasound-guided combined lumbar plexus and sacral plexus block with sedative anesthesia on the prognosis of elderly patients with hip fracture to clarify the clinical value of combined lumbar plexus and sacral plexus block with sedative anesthesia in elderly patients with hip fracture.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anesthesia Morbidity, Anesthesia; Adverse Effect
Keywords
general anesthesia, sacral plexus block, lumbar plexus block, hip fracture, elderly

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1086 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GA group
Arm Type
Experimental
Arm Description
general anesthesia(GA) group: Open peripheral vein fluid infusion, radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring Propofol (1.5-3mg/kg), cis-atracurium(0.1-0.15mg/kg) and sulfentanyl(0.2-0.6μg/kg) anesthesia-induced intubation, mechanical ventilation to maintain normal PETCO2 Use sevoflurane, propofol and sulfentanyl to maintain anesthesia, and add cis-atracurium as needed Transfer to ICU after surgery
Arm Title
CLSB group
Arm Type
Experimental
Arm Description
combined lumbar plexus and sacral plexus block(CLSB) group: Open peripheral vein fluid infusion In lateral position (affected side upward), ultrasound-guided lumbar plexus block (0.375% ropivacaine, Lumbar 2-3 or/and 3-4vertebral space level, 25ml), then sacral plexus block (0.375% ropivacaine, 20ml) Radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring, and blockade effectiveness was evaluated 30min after nerve block After reaching satisfactory blockade, target-controlled infusion of propofol was used to maintain Ramsay sedation score between 5-6 points, monitoring PETCO2 through nasopharyngeal airway, maintain autonomous respiration, and add small-dose fentanyl (10-20μg/time) as needed Transfer to ICU after surgery
Intervention Type
Procedure
Intervention Name(s)
anesthesia
Intervention Description
in this study, we plan to make a prospective, multicenter, randomized controlled clinical trial to compare the effects of general anesthesia with endotracheal intubation and ultrasound-guided combined lumbar plexus and sacral plexus block with sedative anesthesia on the prognosis of elderly patients with hip fracture to clarify the clinical value of combined lumbar plexus and sacral plexus block with sedative anesthesia in elderly patients with hip fracture.
Primary Outcome Measure Information:
Title
mortality
Description
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
Time Frame
month 1
Title
mortality
Description
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
Time Frame
months 3
Title
mortality
Description
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
Time Frame
month 6
Title
mortality
Description
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
Time Frame
month 12
Secondary Outcome Measure Information:
Title
Duration of surgery
Description
The time spent on the surgery will be recorded.
Time Frame
from the start to the end of the surgery
Title
Intraoperative complications
Description
Intraoperative hypotension and vasopressor dosage Intraoperative arrhythmia, myocardial ischemia, myocardial infarction, massive hemorrhage, pulmonary embolism and hypoxemia Intraoperative blood loss and blood transfusion volume
Time Frame
Intraoperative
Title
Incidence of various complications and comprehensive complication index during hospitalization after surgery
Time Frame
up to 8 weeks after the surgery
Title
SOFA score(sequential organ failure assessment score)
Description
Sepsis-related organ failure assessment score, also known as sequential organ failure assessment score (SOFA score), is used to track a person's status during the stay in an intensive care unit (ICU) to determine the extent of a person's organ function or rate of failure. The score is based on six different scores, one each for the respiratory, cardiovascular, hepatic, coagulation, renal and neurological systems.Both the mean and highest SOFA scores are predictors of outcome. An increase in SOFA score during the first 24 to 48 hours in the ICU predicts a mortality rate of at least 50% up to 95%. Scores less than 9 give predictive mortality at 33% while above 11 can be close to or above 95%.
Time Frame
within 3 days after surgery
Title
Length of stay in ICU and hospital
Time Frame
up to 8 weeks after the surgery
Title
the Confusion Assessment Method(CAM)
Description
The Confusion Assessment Method includes an instrument and diagnostic algorithm for identification of delirium.The CAM instrument assesses the presence, severity, and fluctuation of 9 delirium features:acute onset, inattention, disorganized thinking, altered level of consciousness, disorientation, memory impairment, perceptual disturbances, psychomotor agitation or retardation, and altered sleep-wake cycle.
Time Frame
within 3 days after surgery
Title
MMSE(Mini-mental State Examination)
Description
The Mini-Mental State Examination (MMSE) or Folstein test is a 30-point questionnaire that is used extensively in clinical and research settings to measure cognitive impairment. It is commonly used in medicine and allied health to screen for dementia. It is also used to estimate the severity and progression of cognitive impairment and to follow the course of cognitive changes in an individual over time; thus making it an effective way to document an individual's response to treatment. The MMSE test includes simple questions and problems in a number of areas: the time and place of the test, repeating lists of words, arithmetic such as the serial sevens, language use and comprehension, and basic motor skills.
Time Frame
within 3 days after surgery
Title
High-sensitivity cardiac troponin T(hs-cTnT)
Description
Cardiac troponin is the preferred biomarker for the diagnosis of acute myocardial infarction. A high-sensitivity cardiac troponin T(hs-cTnT) assay permits detection of very low levels of cTnT.
Time Frame
1 day before surgery,1 and 3 days after surgery
Other Pre-specified Outcome Measures:
Title
Bauer Patient Satisfaction Questionnaire
Description
Satisfaction with anesthesia care will be assessed on postoperative day 3 via the Bauer Patient Satisfaction Questionnaire. The questionnaire enables a consistent, reliable and valid evalution of patient satisfaction with anesthesia care.
Time Frame
on day 3 after surgery
Title
Economic parameters
Description
Economic parameters including total cost in hospital and expenditure for anesthesia
Time Frame
on day 1 after discharge
Title
Barthel Activities of Daily Living Index
Description
Functional recovery on day 30 after discharge and surgery, evaluated by Barthel Activities of Daily Living Index. Assesses functional independence, generally in stroke patients.
Time Frame
on day 30 after discharge and surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
77 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥77 years old; First unilateral surgery for hip fracture including femoral neck, intertrochanteric or subtrochanteric fracture; Patient with planned hip fracture surgery within 24-72 h; Patient without peripheral nerve block within 24 h prior to surgery; The ability to receive written informed consent from the patient or patient's legal representative. Exclusion Criteria: Refuse to participate; Unable to perform nerve block; Multiple trauma, multiple fractures or other fractures outside the inclusion criteria, such as pathological fractures, pelvic fractures, femur fractures; Prosthetic fracture; Scheduled for bilateral hip fracture surgery; Usage of bone-cement fixation in the surgery; With recent cerebral stroke (<3 months); Combined with active heart disease (unstable angina, acute myocardial infarction, recent myocardial infarction; decompensated heart failure; symptomatic arrhythmia; severe mitral or aortic stenotic heart disease); Patient with known severe lung and/or airway disease, acute respiratory failure, acute pulmonary infection, and acute attack of bronchial asthma; Current enrolment in another clinical trial; Contraindication for general endotracheal anesthesia(drug allergies to general anesthesia, difficult airway); Contraindication for lumbar and sacral plexus block(infection at the site of needle insertion, coagulopathy, allergy to local anesthetics).
Facility Information:
Facility Name
Shanghai Sixth People's Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
021
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaofeng XF Wang, MD
Phone
+8618930170135
Email
240483680@qq.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
30928924
Citation
Zhang J, Wang X, Zhang H, Shu Z, Jiang W. Comparison of combined lumbar and sacral plexus block with sedation versus general anaesthesia on postoperative outcomes in elderly patients undergoing hip fracture surgery (CLSB-HIPELD): study protocol for a prospective, multicentre, randomised controlled trial. BMJ Open. 2019 Mar 30;9(3):e022898. doi: 10.1136/bmjopen-2018-022898.
Results Reference
derived

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Comparison of CLSB With Sedation Versus General Endotracheal Anesthesia on Postoperative Outcomes in Elderly Patients Undergoing Hip Fracture Surgery

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