Comparison between pericapsular nerve group block and lumbar plexus block for hip fracture surgery

Comparison between pericapsular nerve group (PENG) block and lumbar plexus block for hip fracture surgery : a single center randomized, double-blinded study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006929

Enrollment

Registered

2022-01-14

Start date

2022-02-03

Completion date

Unknown

Last updated

2022-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : This is a prospective, randomized, double-blind study conducted at a single institution, and the patient's age, gender, BMI, ASA class, surgical site, preoperative behavior, narcot

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ASA classification I,II,III Patients aged 45 and under 90 who agreed to participate in the study Patients receiving hip surgery conducted by Dong-A university hospital. Patients scheduled to undergo nerve block after consultation with or request from the orthopedic surgeon who will perform the operation

Exclusion criteria

Exclusion criteria: A patient with an infection in the area where the block is performed. Patients with chronic opiates dependence. Patients with morbid obesity (BMI >35) Patients with neurological deficits. Patients who have bleeding tendency Patients with allergies in Ropivacaine Patients with uncontrollable diabetes. Pregnant women Psychosis Rejection of Patients Missing where a survey cannot be conducted on the exclusion criteria

Design outcomes

Primary

Measure	Time frame
Sum of the percentage of complete or mild paralysis at 12 hours after surgery	—

Secondary

Measure	Time frame
Record the time taken for the procedure, the onset of effect, the operation time, and the total anesthesia time. In both groups, the patient's vital signs (blood pressure, oxygen saturation, pulse rate) and pain intensity (NRS score) were 3,6,12,18,24, and 48 hours from the time of entering the recovery room immediately before the procedure, 20 minutes after the procedure, and after the procedure, before the general anesthesia and after the block operation in both groups are checked at rest and during movement by a co-researcher who has not performed the procedure on the subject. In addition, motor and sensory abilities are checked 6, 12, and 24 hours after surgery. And the intensity of postoperative pain is recorded by the patient by filling out a report form. Nausea, vomiting, pruritis, local anesthetic toxicity, urine retention, suspicion of intravascular administration, respiratory failure, transfusion, and delirium should all be recorded. The time at which IV PCA was started for the first time after surgery and the amount of IV PCA used were compared after recording the total amount used during and 24,48 hours after surgery. Also check the time to resume the first step. We also check the number of people who have not received rehabilitation treatment by 24 and 48 hours, respectively. Check the Clavien-Dindo side effect score. We also compare and analyze the discharge preparation date, satisfaction, retry, and quality of sleep.	—

Measure

Time frame

Record the time taken for the procedure, the onset of effect, the operation time, and the total anesthesia time. In both groups, the patient's vital signs (blood pressure, oxygen saturation, pulse rate) and pain intensity (NRS score) were 3,6,12,18,24, and 48 hours from the time of entering the recovery room immediately before the procedure, 20 minutes after the procedure, and after the procedure, before the general anesthesia and after the block operation in both groups are checked at rest and during movement by a co-researcher who has not performed the procedure on the subject. In addition, motor and sensory abilities are checked 6, 12, and 24 hours after surgery. And the intensity of postoperative pain is recorded by the patient by filling out a report form. Nausea, vomiting, pruritis, local anesthetic toxicity, urine retention, suspicion of intravascular administration, respiratory failure, transfusion, and delirium should all be recorded. The time at which IV PCA was started for the first time after surgery and the amount of IV PCA used were compared after recording the total amount used during and 24,48 hours after surgery. Also check the time to resume the first step. We also check the number of people who have not received rehabilitation treatment by 24 and 48 hours, respectively. Check the Clavien-Dindo side effect score. We also compare and analyze the discharge preparation date, satisfaction, retry, and quality of sleep.

—

Countries

Korea, Republic of

Contacts

Public ContactSang Yoong Park

Dong-A University Hospital

parksy@dau.ac.kr+82-51-240-5390

Outcome results