Comparison of CLSB With Sedation Versus General Endotracheal Anesthesia on Postoperative Outcomes in Elderly Patients Undergoing Hip Fracture Surgery
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
1 other identifier
interventional
1,086
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Dec 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 15, 2017
CompletedFirst Posted
Study publicly available on registry
October 23, 2017
CompletedStudy Start
First participant enrolled
December 4, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2023
CompletedAugust 26, 2022
August 1, 2022
5.1 years
October 15, 2017
August 25, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
month 1
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
months 3
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
month 6
mortality
Telephone follow-up will be performed to confirm whether the patient survival or not after surgery.
month 12
Secondary Outcomes (8)
Duration of surgery
from the start to the end of the surgery
Intraoperative complications
Intraoperative
Incidence of various complications and comprehensive complication index during hospitalization after surgery
up to 8 weeks after the surgery
SOFA score(sequential organ failure assessment score)
within 3 days after surgery
Length of stay in ICU and hospital
up to 8 weeks after the surgery
- +3 more secondary outcomes
Other Outcomes (3)
Bauer Patient Satisfaction Questionnaire
on day 3 after surgery
Economic parameters
on day 1 after discharge
Barthel Activities of Daily Living Index
on day 30 after discharge and surgery
Study Arms (2)
GA group
EXPERIMENTALgeneral anesthesia(GA) group: 1. Open peripheral vein fluid infusion, radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring 2. 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 3. Use sevoflurane, propofol and sulfentanyl to maintain anesthesia, and add cis-atracurium as needed 4. Transfer to ICU after surgery
CLSB group
EXPERIMENTALcombined lumbar plexus and sacral plexus block(CLSB) group: 1. Open peripheral vein fluid infusion 2. 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) 3. Radial arterial cannulation under local lidocaine anesthesia and arterial blood pressure monitoring, and blockade effectiveness was evaluated 30min after nerve block 4. 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 5. Transfer to ICU after surgery
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- Refuse to participate;
- Unable to perform nerve block;
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Shanghai Sixth People's Hospital
Shanghai, Shanghai Municipality, 021, China
Related Publications (1)
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.
PMID: 30928924DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Attending doctor
Study Record Dates
First Submitted
October 15, 2017
First Posted
October 23, 2017
Study Start
December 4, 2018
Primary Completion
December 31, 2023
Study Completion
December 31, 2023
Last Updated
August 26, 2022
Record last verified: 2022-08