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Impact of Regional Anesthesia on Chronic Post-operative Pain

Impact of Loco-regional Anesthesia Techniques on Chronic Post-surgery in Breast Oncological Surgery: a Prospective Multicenter Observational Study

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05876390
Acronym
IRACPoP
Enrollment
1500
Registered
2023-05-25
Start date
2022-09-01
Completion date
2026-09-30
Last updated
2026-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

breast cancer, breast surgery, oncological breast surgery, multimodal analgesia, chronic postoperative pain

Brief summary

Approximately 55,000 cases of breast cancer are diagnosed in Italy every year and the first-line therapy for carcinoma in situ, stage I, II and IIIA is surgical removal of the tumour. The incidence of chronic pain after breast cancer surgery is confirmed around 30%. This study aims to evaluate the impact of loco-regional anesthesia techniques in the context of multimodal analgesia in the prevention of chronic pain post-oncological breast surgery

Detailed description

Approximately 55,000 cases of breast cancer are diagnosed in Italy every year and the first-line therapy for carcinoma in situ, stage I, II and IIIA is surgical removal of the tumour. The incidence of chronic pain after breast cancer surgery is confirmed around 30%.Persistent postsurgical pain, defined in the ICD-11 as pain that develops or increases in intensity after a surgical procedure or tissue damage and persists beyond the healing process for at least 3 months after the initial event and is considered a complication of surgery. Several pharmacological and non-pharmacological interventions have been proposed for the prevention of the development of this complication of surgical interventions, including the intraoperative use of local anesthesia techniques in the context of multimodal analgesia. The purpose of this multicenter prospective observational study is to evaluate, through the propensity score methodology, how much the use of loco-regional anesthesia techniques can improve the outcome, in terms of the development of chronic post-surgical pain, of patients undergoing to oncological breast surgery

Interventions

PROCEDUREBreast surgery

Breast surgery

DRUGanalgesia

Multimodal analgesia

Sponsors

Niguarda Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 * Oncological breast surgery: * simple mastectomy, * mastectomy + sentinel lymph node biopsy, * mastectomy + axillary hollowing, * mastectomy + reconstruction, * simple quadrantectomy, * quadrantectomy + sentinel lymph node biopsy, * quadrantectomy + axillary hollowing, * bilateral interventions will also be considered) Exclusion * Age \< 18

Design outcomes

Primary

MeasureTime frameDescription
Incidence of chronic postoperative pain after major breast surgery6 - 12 monthsIncidence of chronic post-surgical pain after major breast surgery (definition: pain that persists at least 3 months after surgery; pain that was not present before surgery or that has different characteristics from pain before surgery or that has increased intensity than before the operation; the pain is localized in the area of the surgical site or in its radiation; other possible causes of pain are excluded)

Secondary

MeasureTime frameDescription
Acute post-operative pain2, 6, 12 and 24 hoursAcute postoperative pain. NRS Numerical Rating Scale (0-10; 0 =better 10= worse outcome)
Chronic post-operative pain3,6,9,12 months) at rest and on mobilizationPain both at rest and on mobilization month3, month6, month9 and month12 after surgery. Numerical Rating Scale (0-10; 0 =better 10= worse outcome)
Quality of life scoreQuality of recovery score (QoR 15)Quality of recovery score-15 (QoR 15; scale 0-150; 0=better 150=worse outcome)
RemifentanylIntraoperativeIntraoperative use of remifentanil. Intraoperative quantitative use of remifentanyl (total micrograms; the lesser the better)
Opioidhour2, hour 6, hour 12 and hour 24 after surgeryPostoperative opioid use. (opioid oral morphine milligram equivalent (MME); the lesser the better)

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 17, 2026