Adults 20 to 65, female only, with Breast Cancer. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Intraoperative Remifentanil ConsumptionPrimary· whole intraoperative period
Intraoperative remifentanil consumption during surgery(whole intraoperative period)
Group
Value
95% CI
Pecs Group
6.75
± 2.18
Control Group
10.12
± 3.68
Sponsor's own description
The purpose of this study is to determine whether pectoral nerves blocks(PECS) would reduces the opioid consumption during the surgery and postoperative pain after breast cancer surgery.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
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· recruiting
NCT07285993 — Detection and Outcomes in Metastatic Invasive Lobular Breast Cancer Through Novel F-18 FAP PET
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· recruiting
NCT07510698 — Same-Day Awake Mastectomy With Immediate Breast Reconstruction for Patients With Breast Cancer
· NA
· recruiting
NCT06768931 — Biolosion Combined Standard Neoadjuvant Therapy to Treat Triple-negative Breast Cancer
· Phase 2
· recruiting
Other Gachon University Gil Medical Center trials
Trials by the same sponsor.
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· recruiting
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NCT06559202 — Inguinal and Axillary LN Size Distribution
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NCT04259918 — Effect of Alveolar Recruitment Maneuver on Postoperative Pain
· NA
· unknown
NCT04238351 — Transnasal Humidified Rapid Insufflation System for Intubation
· NA
· unknown
Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Gachon University Gil Medical Center
Last refreshed: 18 November 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03210220.