NCT03318133

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,086

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Dec 2018

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 15, 2017

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 23, 2017

Completed
1.1 years until next milestone

Study Start

First participant enrolled

December 4, 2018

Completed
5.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2023

Completed
Last Updated

August 26, 2022

Status Verified

August 1, 2022

Enrollment Period

5.1 years

First QC Date

October 15, 2017

Last Update Submit

August 25, 2022

Conditions

Keywords

general anesthesiasacral plexus blocklumbar plexus blockhip fractureelderly

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

EXPERIMENTAL

general 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

Procedure: anesthesia

CLSB group

EXPERIMENTAL

combined 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

Procedure: anesthesia

Interventions

anesthesiaPROCEDURE

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.

CLSB groupGA group

Eligibility Criteria

Age77 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

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

RECRUITING

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.

MeSH Terms

Conditions

Hip Fractures

Interventions

Anesthesia

Condition Hierarchy (Ancestors)

Femoral FracturesFractures, BoneWounds and InjuriesHip InjuriesLeg Injuries

Intervention Hierarchy (Ancestors)

Anesthesia and Analgesia

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

Locations