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Chronic Pain in Post-Mastectomy Patients; The Difference Between Pectoral Nerve (PECS I-II) and Erector Spinal Plane (ESP) Blocks

CompletedNCT06900842
View the official record on ClinicalTrials.gov

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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This study looks at two types of injections (called PECS and ESP blocks) to see which one works better for reducing pain after breast cancer surgery (mastectomy). The main question it asks is: Which block is better at reducing pain after surgery - PECS or ESP? Women who had this surgery and received one of the two blocks were followed for three months. We looked at how much pain they felt, how much pain medication they needed, and whether they still had pain months later. The results showed that both blocks helped with pain right after surgery. The ESP block lasted a little longer at first, but in general, both groups needed about the same amount of pain medicine. Three months later, about half of the patients still had some pain - especially those who had more extensive surgery or had nerve pain early on. There was no big difference between the two blocks when it came to long-term pain.

Study details

Official title
Chronic Pain in Mastectomy Patients; The Difference Between Pectoral Nerve Block (PECS I-II) and Erector Spinal Plane (ESP) Block
Conditions
Sponsor
Hacettepe University
Start date
2024-05-22
Primary completion
2024-09-20
Sex
Female
Age range
from 18 Years to 65 Years
Results posted
No results posted in this snapshot
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Scheduled to undergo modified radical mastectomy due to breast cancer * Decision to perform PECS I-II or ESP block made independently from the study, as part of standard pain management * Aged between 18 and 65 years * American Society of Anesthesiologists (ASA) physical status classification I or II * Female Exclusion Criteria: * Inability to perform the block (e.g., coagulation disorder, allergy to local anesthetics, infection at the injection site) * Obesity (Body Mass Index \> 35 kg/m²) * Pre-existing neurological deficits * Younger than 18 or older than 65 years * ASA physical status classification III or IV * Refusal to give informed consent

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06900842