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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05961735
Other study ID # AnkaraEtlikYusufOzguner004
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2023
Est. completion date June 1, 2024

Study information

Verified date May 2024
Source Ankara Etlik City Hospital
Contact Yusuf Ozguner
Phone +905427150725
Email y.ozguner@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, PECS II block or CSAB will be applied to patients who have had a modified radical mastectomy under general anesthesia for postoperative pain relief by using 30 ml of 0.25% bupivacaine .All patients will receive tramadol with a patient-controlled analgesia device during the postoperative period. Pain, nausea-vomiting, additional analgesic and antiemetic drug requirement, within 24 hours postoperatively will be compared between groups. In this study, it was aimed to compare the efficacy of both peripheral nerve block methods in patients after mastectomy.


Description:

Breast cancer ranks first among the most common malignant neoplasms in women. Surgery has been a mainstay of breast cancer treatment for several decades and historically, a modified radical mastectomy was the primary method of treatment for breast cancer. Poorly controlled acute postoperative pain is associated with increased morbidity, functional and quality-of-life impairment. Additionally, severe acute postoperative pain is found to be a risk factor for chronic pain. Thoracic paravertebral, thoracic epidural, intercostal nerve, and interscalene brachial plexus blocks have been used for anesthesia and abirritation during modified radical mastectomy, but their application is limited due to the complex nature of the procedures and serious complications. There is growing interest in the pectoralis nerve (PECS) blocks and serratus anterior block (SAB) which are less invasive as an analgesic technique during breast surgeries to reduce postoperative pain. The Pecs I block is a single injection of local anaesthetic between pectoralis major and pectoralis minor muscles at the level of the 3rd rib to anaesthetise the lateral and medial pectoral nerves. The Pecs II block is a modified Pecs I block and can be achieved with one needle insertion point. Local anaesthetic is placed between pectorals major and minor as for a Pecs I block and then between pectoralis minor and serratus anterior muscles. Numerous clinical studies focusing on the analgesic potential of PECS block in breast augmentation surgery, small breast surgery and breast cancer surgery have yielded positive results. SAD is more superficial, easy to access and less likely to have complications like PECS block. SAPB can be implemented in two ways. Deep SAB (DSAB) is applied under the serratus anterior muscle, while superficial SAB (YSAB) is applied over the serratus anterior muscle. In recent years, deep and superficial SAB, that is, combined SAB (CSAB), has been started to be applied in order to increase the effect area of local anesthetics and to prevent block failure. In this study, PECS II block or CSAB will be applied to patients who have had a modified radical mastectomy under general anesthesia for postoperative pain relief by using 30 ml of 0.25% bupivacaine .All patients will receive tramadol with a patient-controlled analgesia device during the postoperative period. Pain, nausea-vomiting, additional analgesic and antiemetic drug requirement, within 24 hours postoperatively will be compared between groups. In this study, it was aimed to compare the efficacy of both peripheral nerve block methods in patients after mastectomy.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 1, 2024
Est. primary completion date November 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients between the ages of 18-80 - Patients with ASA score I-II-III - Patients with a body mass index (BMI) between 18 and 40 - Patients who underwent PECS-II block or CSAB with mastectomy in the operating room Exclusion Criteria: - Patients under the age of 18 and over the age of 80 - Patients with an ASA score of IV and above - Patients with advanced co-morbidity - Patients with a history of bleeding diathesis - Patients who have infection in the area which is to be blocked - BMI below 18 and over 40 - Patients undergoing emergency surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
PECS II Block
The Pecs II block is applied to the patients after induction of anesthesia .
Combined Serratus Anterior Plane Block
Combined Serratus Anterior Plane Block is applied to the patients after induction of anesthesia .

Locations

Country Name City State
Turkey Ankara Etlik City Hospital Ankara Varlik Mahallesi, Halil Sezai Erkut Caddesi Yenimahalle
Turkey Yusuf Ozguner Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Etlik City Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Grape S, Jaunin E, El-Boghdadly K, Chan V, Albrecht E. Analgesic efficacy of PECS and serratus plane blocks after breast surgery: A systematic review, meta-analysis and trial sequential analysis. J Clin Anesth. 2020 Aug;63:109744. doi: 10.1016/j.jclinane. — View Citation

Maranto CJ, Strickland NR, Goree JH. Combined Superficial and Deep Serratus Plane Block With Bupivacaine, Dexamethasone, and Clonidine in the Treatment of a Patient With Postmastectomy Pain Syndrome: A Case Report. A A Pract. 2018 Nov 1;11(9):236-237. doi — View Citation

Zhao J, Han F, Yang Y, Li H, Li Z. Pectoral nerve block in anesthesia for modified radical mastectomy: A meta-analysis based on randomized controlled trials. Medicine (Baltimore). 2019 May;98(18):e15423. doi: 10.1097/MD.0000000000015423. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 0 hours postoperatively
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 2 hours postoperatively
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 4 hours postoperatively
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 8 hours postoperatively
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 12 hours postoperatively
Primary Pain on the Numeric Rating Scale (NRS) Participants recorded pain rated on the numeric rating scale (NRS) at 6 time points. NRS range was from 0-10 with 0 being no pain and 10 the worst pain possible. 24 hours postoperatively
Primary Total opioid consumption All patients will receive tramadol with a patient-controlled analgesia device during the postoperative period. 24 hours postoperatively
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