Impact of Erector Spinae Plane Block on Chronic Postsurgical Pain in Breast Cancer Patients
Primary Purpose
Breast Neoplasms, Mastectomy, Nerve Block
Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Erector spinae plane block
Control group
Sponsored by
About this trial
This is an interventional prevention trial for Breast Neoplasms focused on measuring Breast cancer, Mastectomy, Erector spinae plane block, Dexmedetomidine, Postoperative pain, Chronic postsurgical pain, Long-term prognosis
Eligibility Criteria
Inclusion Criteria:
- Age of 18 years or over, but less than 85 years;
- Scheduled to undergo mastectomy for primary unilateral breast cancer.
Exclusion Criteria:
- Previous breast cancer surgery with an incision of >2 cm;
- Chronic opioid dependence or long-term intake of analgesic medicines (>3 months);
- Any contraindication to erector spinae plane block, including intrathoracic infection, infection at the puncture site, cancer invasion of the puncture site, severe spinal deformity, history of spinal surgery, and severe coagulopathy;
- Inability to communicate in the preoperative period because of profound dementia, deafness, language barriers, or end-stage disease;
- History of malignant tumor in other organs, or a current combination of malignant tumor of other organs;
- History of coronary heart disease (diagnosed coronary stenosis, previous myocardial infarction, previous percutaneous coronary intervention or coronary artery bypass grafting); preoperative hepatic or renal impairment (alanine transaminase and/or aspartate transaminase ≥2 times of upper limit of normal, or serum creatinine>133 µmol/L); history of peptic ulcer or hemorrhage; ASA classification IV or above;
- Allergy to ropivacaine.
Sites / Locations
- Peking University First Hospital
- Beijing Cancer Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Erector spinae plane block group
Control group
Arm Description
Prior to general anesthesia, ultrasound guided erector spinae plane block (ESPB; performed with 0.5% ropivacaine 35 ml with dexmedetomidine 1microgram/kg) is performed at T2 level (15 ml) and T4 level (20 ml).
General anesthesia alone.
Outcomes
Primary Outcome Measures
Incidence of chronic postsurgical pain (CPSP) at 6 months after surgery
CPSP is defined as pain persisting for at least three months after surgery that was not present before surgery or that had different characteristics, and other possible causes of pain were excluded (e.g., cancer recurrence, infection).
Progression-free survival (long-term outcomes)
Progression-free survival is defined as the time from randomization to disease progression (recurrence or metastasis) or death from any cause.
Secondary Outcome Measures
Incidence of chronic postsurgical pain (CPSP) at 3 and 12 months after surgery
CPSP is defined as pain persisting for at least three months after surgery that was not present before surgery or that had different characteristics, and other possible causes of pain were excluded (e.g., cancer recurrence, infection).
Incidence of neuropathic pain at 3, 6, and 12 months after surgery
Neuropathic pain is defined as a score at or above 0 on the Neuropathic Pain Questionnaire Short-form. The questionnaire contains three items, i.e., tingling pain, numbness, and increased pain due to touch. Each item is scored from 0 (no pain) to 100 (worst pain imaginable), and multiplied by a discriminant function coefficient (tingling: 0.017, numbness: 0.015, increased pain to touch: 0.011). The total sum of these is added to a constant value (-1.302) to yield a final score ranging from -1.302 to 2.998, with a cutoff of ≥0 suggesting neuropathic pain.
Overall survival (long-term outcome)
Overall survival is defined as the time from randomization to death from any cause.
Event-free survival (long-term outcome)
Event-free survival is defined as the time from randomization to tumor recurrence/metastasis, re-hospitalization for any reason, or death from any cause.
Quality of life (long-term outcome)
Quality of life is assessed with the breast cancer-specific Quality of Life Questionnaire (EORTC QLQ-BR53). It consists of EORTC-C30 [a 30-item questionnaire that provides assessments of functional dimensions (physical, role, cognitive, emotional, social, fatigue, pain, nausea/vomiting, a global health), the total score ranges from 0 to 100, with higher score indicating better function] and EORTC-BR23 [a 23-item questionnaire that provides assessments of symptom dimensions (systemic therapy side effects, arm symptoms, breast symptoms, body image, sexual functioning, sexual enjoyment, feeling of upset due to hair loss, and future perspective), the total score ranges from 0 to 100,with higher score indicating worse symptom].
Full Information
NCT ID
NCT05494502
First Posted
August 8, 2022
Last Updated
April 1, 2023
Sponsor
Peking University First Hospital
Collaborators
Peking University Cancer Hospital & Institute
1. Study Identification
Unique Protocol Identification Number
NCT05494502
Brief Title
Impact of Erector Spinae Plane Block on Chronic Postsurgical Pain in Breast Cancer Patients
Official Title
Impact of Erector Spinae Plane Block With Adjuvant Dexmedetomidine on Chronic Postsurgical Pain in Breast Cancer Patients: a Two-center Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2023 (Anticipated)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
July 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University First Hospital
Collaborators
Peking University Cancer Hospital & Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Chronic postsurgical pain (CPSP) has an incidence of 46% in patients after breast cancer surgery, which seriously affects patients' physiological and psychological function, as well as quality of life. Acute pain is an independent risk factor for persistent pain after surgery. Erector spinae plane block (ESPB) provided excellent perioperative analgesia in patients undergoing breast surgery. Dexmedetomidine as an adjuvant of local anesthetics prolongs the duration of peripheral nerve block and decreases the requirements of postoperative analgesia. The investigators hypothesize that, for breast cancer patients undergoing mastectomy, ESPB (with a combination of 0.5% ropivacaine 35 ml and dexmedetomidine 1 microgram/kg) can reduce the occurrence of CPSP. The purpose of this randomized controlled trial is to investigate the impact of ESPB with adjuvant dexmedetomidine on the incidence of CPSP in breast cancer patients after mastectomy. We will also observe the impact of ESPB on long-term survival in these patients.
Detailed Description
Chronic postsurgical pain (CPSP), defined as pain persisting or recurring for longer than three months after surgery, has an incidence of 46% in patients after breast cancer surgery. It seriously affects patients' physiological and psychological function, as well as quality of life. Acute pain is an independent risk factor for persistent pain after surgery.
As a core technique in multimodal analgesia, peripheral nerve block plays an important role in controlling acute postoperative pain in breast cancer patients; it may also prevent the occurrence of CPSP. In our previous trial, use of paravertebral block reduced CPSP at six months after breast cancer surgery; the effect was more prominent in the subgroup of patients following mastectomy. But conclusions can not be achieved until now. Regional anesthesia is also supposed to produce favorable effects on long-term oncological outcomes, possibly by relieving surgery-related stress response and immunosuppression. But, again, available evidences are conflicting regarding regional block and long-term cancer outcomes.
The erector spinae plane block (ESPB) was first described by Forero in 2016 and provides excellent perioperative analgesia with minimal side effect in patients undergoing thoracic, breast, and spinal surgeries. As one of the interfacial plane block techniques, the ESPB targets dorsal and ventral rami of the spinal nerves from T2-T7; it may produce effect by diffusing into the paravertebral and intercostal spaces and spreading in both cephalic and caudal directions.
Dexmedetomidine is a highly selective α2-adrenoceptor agonist with sedative, analgesic and anti-anxiety properties. When used as an adjuvant to local anesthetics, dexmedetomidine prolongs the duration nerve block and decreased the requirement of postoperative analgesia.
The investigators hypothesize that, for breast cancer patients undergoing mastectomy, ESPB (with 0.5% ropivacaine 35 ml combined with dexmedetomidine 1 microgram/kg) can reduce the occurrence of CPSP. The purpose of this randomized controlled trial is to investigate the impact of ESPB with adjuvant dexmedetomidine on the incidence of CPSP in breast cancer patients after mastectomy. We will also observe the effect of ESPB on long-term prognosis in this patient population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasms, Mastectomy, Nerve Block, Dexmedetomidine, Pain, Postoperative, Chronic Pain, Prognosis
Keywords
Breast cancer, Mastectomy, Erector spinae plane block, Dexmedetomidine, Postoperative pain, Chronic postsurgical pain, Long-term prognosis
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1206 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Erector spinae plane block group
Arm Type
Experimental
Arm Description
Prior to general anesthesia, ultrasound guided erector spinae plane block (ESPB; performed with 0.5% ropivacaine 35 ml with dexmedetomidine 1microgram/kg) is performed at T2 level (15 ml) and T4 level (20 ml).
Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
General anesthesia alone.
Intervention Type
Procedure
Intervention Name(s)
Erector spinae plane block
Intervention Description
Prior to general anesthesia, ultrasound guided erector spinae plane block (ESPB; performed with 0.5% ropivacaine 35 ml with dexmedetomidine 1 microgram/kg) is performed at T2 level (15 ml) and T4 level (20 ml).
Intervention Type
Procedure
Intervention Name(s)
Control group
Intervention Description
General anesthesia alone.
Primary Outcome Measure Information:
Title
Incidence of chronic postsurgical pain (CPSP) at 6 months after surgery
Description
CPSP is defined as pain persisting for at least three months after surgery that was not present before surgery or that had different characteristics, and other possible causes of pain were excluded (e.g., cancer recurrence, infection).
Time Frame
At 6 months after surgery
Title
Progression-free survival (long-term outcomes)
Description
Progression-free survival is defined as the time from randomization to disease progression (recurrence or metastasis) or death from any cause.
Time Frame
Up to 3 years after surgery
Secondary Outcome Measure Information:
Title
Incidence of chronic postsurgical pain (CPSP) at 3 and 12 months after surgery
Description
CPSP is defined as pain persisting for at least three months after surgery that was not present before surgery or that had different characteristics, and other possible causes of pain were excluded (e.g., cancer recurrence, infection).
Time Frame
At 3 and 12 months after surgery
Title
Incidence of neuropathic pain at 3, 6, and 12 months after surgery
Description
Neuropathic pain is defined as a score at or above 0 on the Neuropathic Pain Questionnaire Short-form. The questionnaire contains three items, i.e., tingling pain, numbness, and increased pain due to touch. Each item is scored from 0 (no pain) to 100 (worst pain imaginable), and multiplied by a discriminant function coefficient (tingling: 0.017, numbness: 0.015, increased pain to touch: 0.011). The total sum of these is added to a constant value (-1.302) to yield a final score ranging from -1.302 to 2.998, with a cutoff of ≥0 suggesting neuropathic pain.
Time Frame
At 3, 6 and 12 months after surgery
Title
Overall survival (long-term outcome)
Description
Overall survival is defined as the time from randomization to death from any cause.
Time Frame
Up to 3 years after surgery
Title
Event-free survival (long-term outcome)
Description
Event-free survival is defined as the time from randomization to tumor recurrence/metastasis, re-hospitalization for any reason, or death from any cause.
Time Frame
Up to 3 years after surgery
Title
Quality of life (long-term outcome)
Description
Quality of life is assessed with the breast cancer-specific Quality of Life Questionnaire (EORTC QLQ-BR53). It consists of EORTC-C30 [a 30-item questionnaire that provides assessments of functional dimensions (physical, role, cognitive, emotional, social, fatigue, pain, nausea/vomiting, a global health), the total score ranges from 0 to 100, with higher score indicating better function] and EORTC-BR23 [a 23-item questionnaire that provides assessments of symptom dimensions (systemic therapy side effects, arm symptoms, breast symptoms, body image, sexual functioning, sexual enjoyment, feeling of upset due to hair loss, and future perspective), the total score ranges from 0 to 100,with higher score indicating worse symptom].
Time Frame
At 1 year, 2 years, and 3 years after surgery
Other Pre-specified Outcome Measures:
Title
Pain intensity within the first 3 postoperative days
Description
Pain intensity is assessed with the numeric rating scale, an 11-point scale where 0=no pain and 10=the worst pain, both at rest and with movement.
Time Frame
At 1 hour, 6 hours, 1 day, 2 days, and 3 days after surgery.
Title
Subjective sleep quality within the first 3 postoperative days
Description
Subjective sleep quality is assessed with the numeric rating scale, an 11-point scale where 0=the best sleep quality and 10=the worst sleep quality.
Time Frame
At 1 hour, 6 hours, 1 day, 2 days, and 3 days after surgery.
Title
Patient-reported quality of recovery
Description
Patient-reported quality of recovery is assessed with the Quality of Recovery-15 scale (QoR-15 scale, a 15-item scale to assess the patients' postoperative recovery in physical comfort, emotional state, physical independence, psychological support and pain. For each item, the score ranges from 0 to 10. The total score ranges from 0 to 150, with higher score indicating better recovery).
Time Frame
At day 1 after surgery
Title
Length of stay in hospital after surgery
Description
Length of stay in hospital after surgery
Time Frame
Up to 30 days after surgery
Title
Incidence of postoperative complications within 30 days
Description
Postoperative complications are generally defined as newly occurred medical conditions that are deemed harmful and required therapeutic intervention within 30 days after surgery.
Time Frame
Up to 30 days after surgery
Title
Incidence of anxiety at 30 days after surgery
Description
Anxiety is defined as a score of 8 or above on the anxiety subscale of the Hospital Anxiety and Depression Scale.
Time Frame
At 30 days after surgery
Title
Incidence of depression at 30 days after surgery
Description
Depression is defined as a score of 8 or above on the depression subscale of the Hospital Anxiety and Depression Scale.
Time Frame
At 30 days after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age of 18 years or over, but less than 85 years;
Scheduled to undergo mastectomy for primary unilateral breast cancer.
Exclusion Criteria:
Previous breast cancer surgery with an incision of >2 cm;
Chronic opioid dependence or long-term intake of analgesic medicines (>3 months);
Any contraindication to erector spinae plane block, including intrathoracic infection, infection at the puncture site, cancer invasion of the puncture site, severe spinal deformity, history of spinal surgery, and severe coagulopathy;
Inability to communicate in the preoperative period because of profound dementia, deafness, language barriers, or end-stage disease;
History of malignant tumor in other organs, or a current combination of malignant tumor of other organs;
History of coronary heart disease (diagnosed coronary stenosis, previous myocardial infarction, previous percutaneous coronary intervention or coronary artery bypass grafting); preoperative hepatic or renal impairment (alanine transaminase and/or aspartate transaminase ≥2 times of upper limit of normal, or serum creatinine>133 µmol/L); history of peptic ulcer or hemorrhage; ASA classification IV or above;
Allergy to ropivacaine.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zeng-Mao Lin, M.D.
Phone
+86 13810098351
Email
linzengmao@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Dong-Xin Wang, M.D., Ph.D.
Phone
+86 13910731903
Email
wangdongxin@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dong-Xin Wang, M.D., Ph.D.
Organizational Affiliation
Peking University First Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University First Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100034
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zeng-Mao Lin, M.D.
Phone
+86 13810098351
Email
Linzengmao@163.com
Facility Name
Beijing Cancer Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100142
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ling Yu, M.D.
Phone
+86 13146203116
Email
fishyu071@sina.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Impact of Erector Spinae Plane Block on Chronic Postsurgical Pain in Breast Cancer Patients
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