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Analgesic Effect to Postoperative Pain After Mastectomy: Ultrasound-guided Serratus Anterior Plane Block

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02483923
Enrollment
40
Registered
2015-06-29
Start date
2015-06-16
Completion date
2016-02-28
Last updated
2018-07-17

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

Conditions

Breast Cancer

Keywords

serratus anterior block, ultrasound, breast cancer, postoperative pain

Brief summary

Ultrasound guided serratus anterior plane block may decrease acute postoperative pain and consumption of opioid after mastectomy.

Interventions

DRUGUltrasound guided serratus anterior block with ropivacaine

After induction of anesthesia, patients take ultrasound guided serratus anterior plane block with 0.5ml/kg of ropivacaine 0.375%. 30minutes before the end of operation, intravenous patient controlled analgesia (Basal rate 0ml/hr, 0.5mcg/kg of fentanyl, lock-out time 10minutes) is connected to patient.

DRUGintravenous PCA only

same dose of intravenous patient controlled analgesia (Basal rate 0ml/hr, 0.5mcg/kg of fentanyl, lock-out time 10minutes) is connected to patient only.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. ASA 1\ 3 2. Age 20\ 80 3. Breast cancer patient twho are scheduled for elective mastectomy

Exclusion criteria

1. Allergy to local anesthetics or contraindication to use of ropivacaine 2. Pregnancy 3. Severe cardiovascular disease 4. Renal failure 5. Liver failure 6. Neurologic and psychologic disease 7. Chronic treatment with analgesics 8. Previous history of mastectomy or thoracic surgery.

Design outcomes

Primary

MeasureTime frameDescription
Total opioid consumptionwithin 24 hrs after mastectomyAssessing total opioid consumption (total number of bolus injection and total dose of fentanyl via intravenous patient controlled analgesia) within 24hours after operation finished.

Secondary

MeasureTime frame
Postoperative pain scale (Numeric rating scale 0-10) at PACUchang from 3,6,12,24 to 48hrs after operation end
Total intraoperative remifentanil consumption(mcg)within 24 hrs after mastectomy
Additional analgesics requirements (dose/number)within 24 hrs after mastectomy
incidence and intensity of postoperative nausea and vomiting(NRS:0-10)within 24 hrs after mastectomy
Total hospital staying timewithin 24 hrs after mastectomy

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026