Clinical Trials Logo
  1. Home
  2. Postoperative Analgesia
  3. NCT04886375
  4. Details
NCT04886375 Clinical Trial

Comparison of USG- Guided Modified Pectoral Nerve Block and Erector Spinae Plane Block on Postoperative Analgesia in Video Assisted Thoracoscopic Surgery

Postoperative Analgesia Clinical Trial

Official title:
The Effect of USG- Guided Modified Pectoral Nerve Block and Erector Spinae Plane Block on Postoperative Analgesia in Video Assisted Thoracoscopic Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04886375
Other study ID # 2019-124
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date April 1, 2020

Study information
Verified date May 2021
Source Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to compare the effects of the erector spinae plan block (ESP) and modified pectoral nerve block (PECS II) on postoperative analgesia in patients undergoing video- assisted thoracoscopic surgery (VATS).

Description:

55 patients (ASA I-II-III) between 18 and 65 years of age, who were to undergo VATS, were randomized and divided into two groups. (26 patients in each of the PECS and ESP groups). Three patients were excluded from the study because thoracotomy was performed. ESP block was performed for ESP group and a modified pectoral nerve block was performed in the PECS group. Postoperative analgesia was provided by intravenous morphine infusion using a patient-controlled analgesia device. Postoperative 24-hour total morphine consumption and duration of analgesia were the primary outcome measure. Perioperative remifentanil use, numeric rating scale values, time of the first analgesic request, and additional analgesic consumption were recorded.

Recruitment information / eligibility
Status Completed
Enrollment 55
Est. completion date April 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Ages of 18-65 - Patients who will undergo VATS - ASA I-II-III patients Exclusion Criteria: - Clinically diagnosis of spinal or chest wall deformity or pathology - Clinically known local anesthetic allergy - Morbid obesity (body mass index>40 kg m2) - Clinically diagnosis of opioid, alcohol and substance dependence - Clinically diagnosis of psychiatric disease - Coagulopathy - Patients with ASA IV-V

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• erector spina plane block
The investigators performed erector spina plane block to that patient group for postoperative analgesia
• modified pectoral nerve block
The investigators performed modified pectoral block to that patient group for postoperative analgesia

Locations
Country Name City State
Turkey Bakirkoy Dr. Sadi Konuk Research and Training Hospital Istanbul Bakirkoy

Sponsors (1)
Lead Sponsor Collaborator
Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative 24-hours total morphine consumption This will be measured only one time by pca device at the 24th hour after surgery. 24 hours postoperatively
Secondary NRS scores of patients NRS at 0, 1, 2, 4, 8, 12 ve 24th hours 24 hours postoperatively
See also
  Status Clinical Trial Phase
Completed NCT05023850 - Comparing Thoracolumbar Interfascial Plane Block With Erector Spinae Plane Block N/A
Completed NCT06205199 - Analgesic Effect of Ropivacaine Combined With Hydromorphone for CSEA After Total Knee Arthroplasty N/A
Not yet recruiting NCT06062550 - Different Dose Esketamine and Dexmedetomidine Combination for Supplemental Analgesia After Scoliosis Correction Surgery Phase 4
Completed NCT03239314 - Analgesic Effect of Adductor Canal Block With and Without Dexamethasone for Knee Arthroscopy N/A
Completed NCT05317572 - Comparison of Three Different Doses of Intrathecal Morphine for Analgesia After Cesarean Section N/A
Recruiting NCT06157359 - Effect of SNB on the QoR in Patients Undergoing Supratentorial Tumor Resection N/A
Completed NCT03258255 - Analgesic Efficiency of Pudendal Nerve Block Versus Penil Block for Circumsion in Children N/A
Recruiting NCT06078241 - Postoperative Analgesia in Patients Undergoing Percutaneous Nephrolithotomy N/A
Recruiting NCT06430112 - Liposomal Bupivacaine vs Ropivacaine for TAPBs Phase 3
Completed NCT04579302 - Serratus Anterior Block and Erector Spinae Block in Postoperative Analgesia N/A
Completed NCT04111848 - Magnesium and Ketamine in Postoperative Analgesia Phase 4
Completed NCT03341234 - Superficial Serratus Plane Block for Modified Radical Mastectomy and Axillary Lymph Node Disection N/A
Recruiting NCT03540537 - A Trial Comparing Quadratus Lumborum Block (QLB) and Paravertebral Block (PVTB) for Postoperative Analgesia in Hepatectomy N/A
Terminated NCT02150161 - Opioid vs. Opioid-free Anesthesia for Hip Arthroscopy Phase 3
Not yet recruiting NCT01589354 - Effectiveness of Interscalene Brachial Plexus Block and Intra-articular Injection of Ropivacaine for Post-operative Analgesia in Arthroscopic Shoulder Stabilization Surgery N/A
Completed NCT05855798 - Ketamine and Magnesium in Erector Spinae Plane Block Phase 4
Not yet recruiting NCT04845711 - Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block in Laparoscopic Cholecystectomy N/A
Completed NCT03131375 - Dexmedetomidine Reduces Emergence Delirium in Children Undergoing Tonsillectomy With Propofol Anesthesia Phase 2/Phase 3
Completed NCT03885427 - Analgo-Sedative Effects Of Oral, Or Nebulized Ketamine In Pre-schoolers Undergoing Elective Surgery. Early Phase 1
Completed NCT04738357 - A Clinical Study to Evaluate Efficacy and Safety of HSK21542 for Postoperative Analgesia of Subjects Undergoing Elective Laparoscopic Surgery Under General Anesthesia Phase 3