Comparison of Perioperative Analgesic Efficacy of Femoral Nerve Block, Adductor Canal Block and 4in1 Block

Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05643040
Collaborator
(none)
60
1
3
8
7.5

Study Details

Study Description

Brief Summary

Central neuraxial and regional anesthesia and analgesia techniques significantly reduce perioperative morbidity and mortality in the knee and below-knee surgeries.Nerve blocks appear to have better analgesic efficacy compared to placebo or patient-controlled analgesia (PCA). In addition, opioid-related side effects such as postoperative nausea, vomiting, pruritus, sedation, and respiratory depression are less. Therefore, interest in regional blocks such as femoral, sciatic, adductor, combined femoral, and sciatic is increasing. The knee joint is innervated by various nerves (genicular nerves) from the femoral, obturator, and sciatic nerves, and a comprehensive but simple technique is needed for postoperative analgesia. Complete and comprehensive postoperative analgesia was possible with this block, a simple single injection technique. The aim of our study is to evaluate the intraoperative analgesia efficacy of femoral, adductor canal block, and 4in1 block in patients who will undergo knee surgery.

Condition or Disease Intervention/Treatment Phase
  • Other: femoral nerve block
  • Other: adductor canal block
  • Other: 4in1 block
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Group I: Femoral nerve block Group II: Adductor canal block Group III: 4in1 blockGroup I: Femoral nerve block Group II: Adductor canal block Group III: 4in1 block
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
Comparison of Perioperative Analgesic Efficacy in Patients Who Had Femoral Nerve Block, Adductor Canal Block and 4in1 Block Applied in Knee Surgery
Actual Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: femoral nerve block

To evaluate the intraoperative analgesia effectiveness of femoral nerve block in patients who will have knee surgery.

Other: femoral nerve block
To evaluate the intraoperative analgesia effectiveness of femoral block in patients who will have knee surgery.

Experimental: adductor canal block

To evaluate the intraoperative analgesia effectiveness of adductor canal block in patients who will have knee surgery.

Other: adductor canal block
To evaluate the intraoperative analgesia effectiveness of adductor canal block in patients who will have knee surgery.

Experimental: 4in1 block

To evaluate the intraoperative analgesia effectiveness of 4in1 block in patients who will have knee surgery.

Other: 4in1 block
To evaluate the intraoperative analgesia effectiveness of 4in1 block in patients who will have knee surgery.

Outcome Measures

Primary Outcome Measures

  1. intraoperative analgesia efficacy [perioperative period]

    The aim of our study is to evaluate the intraoperative analgesia efficacy of femoral, adductor canal block and 4in1 block in patients who will undergo knee surgery.

Secondary Outcome Measures

  1. postoperative analgesia efficacy [perioperative period]

    The aim of our study is to evaluate the postoperative analgesia efficacy of femoral, adductor canal block and 4in1 block in patients who will undergo knee surgery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients between the ages of >18

  • undergone knee surgery

  • American Society of Anesthesiologists (ASA) classification I-III group.

Exclusion Criteria:
  • Patients who do not want to participate in the study coagulopathy peripheral neuropathy local anesthetic drug allergy chronic opioid users anticoagulant users pregnant patients

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Medical Science, Yıldırım Beyazıt Training and Research Hospital Ankara Turkey 06000

Sponsors and Collaborators

  • Diskapi Yildirim Beyazit Education and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Funda Atar, Diskapi Yildirim Beyazit Education and Research Hospital, Diskapi Yildirim Beyazit Education and Research Hospital
ClinicalTrials.gov Identifier:
NCT05643040
Other Study ID Numbers:
  • 06/06/2022 139/13
First Posted:
Dec 8, 2022
Last Update Posted:
Dec 8, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Funda Atar, Diskapi Yildirim Beyazit Education and Research Hospital, Diskapi Yildirim Beyazit Education and Research Hospital

Study Results

No Results Posted as of Dec 8, 2022