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Evaluation of the Effect of Pectoral Nerve Block II on Acute and Chronic Pain in Patients Undergoing Oncological Breast Surgery

I

Irem Erkan

Status

Completed

Conditions

Chronic Pain
Breast Carcinoma

Study type

Observational

Funder types

Other

Identifiers

NCT06718868
E-48670771-514.99-232052317

Details and patient eligibility

About

The aim of this observational study is to evaluate the effect of Pectoral Nerve Block II (PECSII) on the development of pain in the acute and chronic periods in female patients over the age of 18 who underwent oncological breast surgery. The main questions it aims to answer are:

Is PECSII blockade applied to patients undergoing oncological breast surgery effective on acute pain scores compared to the non-blockade group? Is there a difference between the group with block and the group without block in terms of the development of chronic pain in the evaluation made at the 3rd month after surgery? The analgesia method applied to the patients will be recorded in the patient files and acute and chronic pain scores will be evaluated. Chronic pain score evaluation will be made by telephone survey.

Enrollment

128 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who will be operated under general anesthesia
  • ASA score I-II-III patients
  • Non-pregnant patients
  • Patients who agreed to participate in the study

Exclusion criteria

  • Patients with coagulopathy
  • Patients who underwent bilateral mastectomy
  • Patients with chest wall anomalies
  • Patients with neuropathic pain before surgery
  • Patients who did not agree to participate in the study

Trial design

128 participants in 2 patient groups

Group 1
Description:
Patients in Group 1 were defined as those who received PECSII Block in addition to intravenous analgesia.
Group 2
Description:
Patients in Group 2 were defined as patients who received intravenous analgesia only.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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