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Comparison of postoperative analgesic effects after breast surgery between thoracic paravertebral block and erector spinae plane block

Comparison of postoperative analgesic effects after breast surgery between thoracic paravertebral block and erector spinae plane block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200105003
Enrollment
Unknown
Registered
2020-01-05
Start date
2020-01-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Breast cancer Breast cancer Breast surgery Postoperative pain control Thoracic paravertebral block Erector spinae plane block

Interventions

Performing ultrasound-guided erector spinae plane block at thoracic spine level T4, using levobupivacaine 20 mL, before induction of anesthesia,Performing ultrasound-guided thoracic paravertebral bloc
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
Erector spinae plane block,Thoracic paravertebral block

Sponsors

Khon Kaen University
Lead Sponsor
Khon Kaen University
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients age 18-75 years 2. ASA physical status of 1-3 3. Able to communicate and understand the communication

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to enter the study 2. Pregnant patient or in the duration of breast-feeding the baby 3. Patients that have bleeding disorder 4. Patients with skin infection at regional anesthesia procedure site 5. Patients who allergic to local anesthetics agents or other medicine used in the study 6. Body mass index more than 35 7. Currently on morphine or opioid derivatives treatments 8. Body weight less than 40 kg

Design outcomes

Primary

MeasureTime frame
Opioid consumption 24 hr mg

Secondary

MeasureTime frame
Opioid consumption 1 hr mg,Opioid consumption 6 hr mg,Opioid consumption 12 hr mg,Opioid consumption 48 hr mg,Pain score at rest 1 hr Pain score assessment by numerical rating scale 0-10,Pain score at rest 6 hr Pain score assessment by numerical rating scale 0-10,Pain score at rest 12 hr Pain score assessment by numerical rating scale 0-10,Pain score at rest 24 hr Pain score assessment by numerical rating scale 0-10,Pain score at rest 48 hr Pain score assessment by numerical rating scale 0-10,Pain score on movement 1 hr Pain score assessment by numerical rating scale 0-10,Pain score on movement 6 hr Pain score assessment by numerical rating scale 0-10,Pain score on movement 12 hr Pain score assessment by numerical rating scale 0-10,Pain score on movement 24 hr Pain score assessment by numerical rating scale 0-10,Pain score on movement 48 hr Pain score assessment by numerical rating scale 0-10,Level of sensory blockade after nerve block Level of cold sensation blockade tested by alcohol,Complications: respiratory depression, pneumothorax, LASTs, sedation, nausea and vomiting 1,6,12,24,48 hr Observation and surveys

Countries

Thailand

Contacts

Public ContactNattanan Sinthuchao

Srinagarind hospital

sinthuchaon@yahoo.com0876549907

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026