Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04860843
Other study ID # H20-00787
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 1, 2021
Est. completion date August 2024

Study information

Verified date January 2024
Source University of British Columbia
Contact Kathryn Isaac, MD MPH FRCSC
Phone 604-827-0438
Email kathryn.isaac@ubc.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pain management is a major concern in oncologic breast surgery and reconstruction. Significant risks for acute and chronic pain after surgery might be reduced through improved pain control pre-operatively. Addition of regional anesthesia to a multimodal peri-operative pain management protocol offers a promising solution for improved recovery. For patients undergoing mastectomy with immediate alloplastic breast reconstruction, this RCT compares TPVB+Pecs local anesthetic block with TPVB local anesthetic block and Pecs placebo normal saline block for their effect on acute pain, chronic pain, opioid consumption, opioid-related side effects, patient-reported quality of recovery after surgery, and length of stay.


Description:

OBJECTIVES The primary objectives of the pilot trial are to demonstrate feasibility of recruitment and to demonstrate efficacy potential. The primary objectives of the definitive trial are to determine if Thoracic Paravertebral with Pecs blocks (defined as Pec I and Pec II blocks) (TPVB+Pecs) will reduce opioid consumption and chronic pain compared to a TPVB+Sham block in patients undergoing mastectomy with IBR using tissue expanders or implants. Secondary objectives of the definitive trial include assessment of opioid consumption, patient-reported postoperative pain scores, postoperative nausea and vomiting, length of stay, and patient-reported quality of recovery. HYPOTHESIS In breast cancer patients undergoing mastectomy with immediate implant-based breast reconstruction, the addition of a Pecs block to a thoracic paravertebral block (TPVB+Pecs) will reduce acute and chronic patient-reported postoperative pain as compared to a thoracic paravertebral block with sham Pecs block (TPVB+Sham). Secondary hypotheses include: the TPVB+Pecs over TPVB+Sham will decrease opioid consumption, postoperative nausea and vomiting, decrease patient-reported postoperative pain scores, length of stay, and improve patient-reported quality of recovery in patients undergoing total mastectomy with IBR using tissue expanders or immediate implants. JUSTIFICATION The definitive trial will determine if TPVB+Pecs improves postoperative acute and chronic pain and reduces opioid use for patients undergoing mastectomy with IBR using tissue expanders or immediate implants. International Consensus guidelines for ERAS in breast reconstruction make a strong recommendation for multimodal, opioid-sparing analgesia postoperatively based on high-level evidence. Increased total opioid analgesic use has been shown to increase length of stay in hospital. Reduced opioid consumption results in less postoperative nausea, vomiting, and constipation, supports early ambulation, shortens hospital stays, and improves psychological well being. Current ERAS protocols for alloplastic breast reconstruction are successfully opioid-sparing and address acute recovery. However, opioids continue to play an important role in peri-operative protocols for achieving adequate pain control, which suggests further adjunctive strategies may be beneficial. Furthermore, the effects of peri-operative protocols on the development of chronic pain are lacking. By evaluating the effectiveness of TPVB+Pecs in alloplastic reconstruction, our proposed study would help to establish an important additional feature to the ERAS pathway for our hospital and other institutions. STUDY DESIGN The design of the pilot RCT is the same as the future definitive trial, a parallel-group, double-blinded RCT. The target population includes patients undergoing mastectomy with IBR using tissue expanders or immediate implants. The study will compare two arms: 1. TPVB using local anesthetic infiltrate with Pecs using local anesthetic infiltrate (TPVB+Pecs, the intervention arm). OR 2. TPVB using local anesthetic infiltrate with Pecs using normal saline infiltrate (TPVB+Sham, the control arm). The pilot trial will be conducted at Mount Saint Joseph Hospital (MSJH). The assignment of intervention will be determined by randomization through REDCap. Each participant will be assigned a consecutive Study ID at time of enrollment. Patients will be randomized 1:1 to either TPVB+Pecs or TPVB+Sham. Patients undergoing symmetrizing procedures as part of a bilateral breast surgery will not have a regional block on the symmetrizing side (which is not IBR). Patients undergoing bilateral IBR surgery using implants or expanders on both breasts will not be included in the study due to risk of local anesthetic toxicity with bilateral TPVB. The randomization sequence will be created using REDCap-generated 1:1 randomization with permuted blocks of varying size (4 and 6). The assignments (TPVB+Pecs or TPVB+Sham) will be placed in order in opaque, consecutively numbered envelopes. The sequence and envelopes will be created by an independent research assistant who will not be involved in the remainder of the study implementation. Study participants, Operating Room (OR) anesthesiologists, surgeons, research assistants, and nurses in the OR, Post-anesthesia Care Unit (PACU), and ward will be blinded as to whether a participant receives TPVB+Pecs or TPVB+Sham block. At MSJH, the anesthesiologists in the operative theater are separate from the team of regional anesthesiologists performing regional blocks in the preoperative area. Only the regional anesthesiologist and anesthesia assistant in the preoperative block area, who will administer the regional block, will be unblinded. On the day of surgery, the regional anesthesiologist at MSJH will be provided with the Study ID specific sealed envelope which will assign the patient to receive either the TPVB+Pecs or TPVB+Sham block. The regional anesthesiologist will prepare local anesthetic or normal saline injections for infiltration based on the random assignment. For all patients, the regional block will be performed as outlined in the Procedure Protocols (See Appendix 1: Nerve Block). All participants will receive general anesthesia following the nerve block. All other parameters and protocols will be identical. Currently, at MSJH, approximately 4 - 5 cases of mastectomy with IBR are performed per week. We do not anticipate difficulty with enrolment into this study. This internal pilot will generate initial recruitment data to enable an early review and validation of our recruitment projections and study population target prior to transition to formal RCT. Additional Details of Study Design Participants will also be given at the time of consent a post operative package. This will contain the Quality of Recovery-15 Questionnaire (Form 7), Recovery Booklet (Form 5) and Pain Burden Index (Form 8). The Quality of Recovery-15 Questionnaire (see Form 7) is to be completed at 24 hours after surgery in paper format or electronic format (based on their preference). This 24 hour time point will be marked on the QoR-15 form. If paper format is preferred, the QoR-15 will be provided with a paid-postage envelope to return once completed at 24 hours after surgery. The pain NRS at 24 hours will be recorded from the chart. The envelopes will be addressed to the research coordinator at UBC Hospital office. If the participant prefers electronic format, the questionnaire will be sent to their provided email address using secure online format (REDCap developed questionnaire). Recovery Booklet (see Form 5) will include: a) schedule for taking prescription pain medications; b) a postoperative 7-day symptom diary (for recording pain on NRS at 24 hours, episodes of vomiting, nausea, and use of prescribed medications). Patients will be provided with a paid-postage envelope to return their Recovery Booklet via mail once completed 7 days after surgery. Patients will be reminded to complete the Recovery Booklet (Form 5) in 3-4 days and once again at 14 days to return the envelope. The Pain Burden Index questionnaire (see Form 8) asks specifically about pain in four surgically related body areas and to calculate the Pain Burden Index (PBI). The PBI is calculated by summing the pain severity scale (0-10) at each of four locations (breast, axilla, chest wall, arm) multiplied by the frequency of the pain at each site. The PBI questionnaire will be sent to participants via mail as paper format (with paid-postage envelope to return once completed) or email as electronic format (as per their requested preference) to be completed 3 and 6 months after their surgery. Details of present adjuvant treatments (radiation and chemotherapy) will also be included in the questionnaire. Secondary outcomes data including opioid consumption and side effects, length of stay in hospital (hours), rescue medications, failure of early discharge, complications and adverse events and time-based outcome measures (time in PACU, time under general anesthesia, time to perform ultrasound-guided TPVB+PecsII, failure of discharge from PACU and requiring admission) will be collected through participants' charts and EMR. STATISTICAL ANALYSIS Patient characteristics and outcome measures will be summarized by group. An 80% confidence interval for the difference in average pain score over 24 hours will be calculated.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date August 2024
Est. primary completion date May 2024
Accepts healthy volunteers No
Gender Female
Age group 19 Years and older
Eligibility Inclusion Criteria: 1. Patients must be female, and at least 19 years old. 2. Patients must be ASA grade I or II. 3. Patients must be undergoing total mastectomy with IBR using tissue expander or implant, with or without axillary surgery. Exclusion Criteria: 1. Patients have a known contraindication for a regional block: known coagulation disorder, treatment with anticoagulants, infection at the injection site, known allergy to medication in the study. 2. Patients who are pregnant at the time of surgery. 3. Patients having bilateral mastectomy and immediate alloplastic breast reconstruction (as only one side can be blocked to prevent local anesthesia toxicity). 4. Patients with ASA Class III or IV. 5. Patients with BMI>35kg/m2. 6. Patients weighing less than 50kg. 7. Patients living/staying outside of 1-hour driving distance from hospital.

Study Design


Intervention

Drug:
Thoracic paravertebral block
Participants will receive a thoracic paravertebral with local anesthetic infiltrate (30ml of 0.35% ropivacaine with 1:400K epinephrine).
Pecs block
Participants will receive a pecs block with local anesthetic infiltrate (30ml of 0.25% ropivacaine with 1:400K epinephrine).
Sham Pecs block
Participants will receive a and a pecs block with saline infiltrate (30ml normal saline; 0.9% NaCl).

Locations

Country Name City State
Canada Mount St Joseph Hospital Vancouver British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of participant recruitment The definitive trial will be considered feasible if > 50% of eligible patients are enrolled in this pilot study. 1 year
Primary Rate of successful nerve blocks The definitive trial will be considered feasible if > 90% of blocks are successful. 1 year
Primary Rate of participant retention The definitive trial will be considered feasible if there is > 90% participant retention at 6 months. 6 months
Primary Average pain score in the 24-hour post-operative period assessed by the Numerical Rating Scale. The Numerical Rating Scale is an 11-point scale (0-10), where a lower number indicates less pain. We will consider preliminary evidence of efficacy for a definitive trial if the 80% confidence interval for the between-group difference in average pain score in the 24-hour postoperative period favours LA block. 24 hours post-operatively
Secondary Opioid analgesia requirements Will include intraoperative opioids administered in the OR and postoperative opioids administered/ingested in the Postanesthetic Care Unit (PACU), Surgical Day Care Unit (SDC), Inpatient Unit, and home in the 24-hour period after completion of surgery. Opioids consumed will be converted to MME. 24 hours post-operatively
Secondary Acute patient-reported pain scores assessed by the Numerical Rating Scale The Numerical Rating Scale is an 11-point scale (0-10), where a lower number indicates less pain). It will be measured at the standard time points of nursing care assessments: preoperatively (baseline); four times per hour in PACU until discharge; if admitted, hourly for 2 hours, and then every 6 hours in the Inpatient Unit; and at discharge from hospital; 24 hours after surgery is complete. Up to 24 hours post-operatively
Secondary Post-operative nausea measured by the Numerical Rating Scale The Numerical Rating Scale is an 11-point scale (0-10), where a higher score indicates a better outcome/ less nausea. 24 hours post-operatively
Secondary Post-operative vomiting measured by number of vomiting episodes Number of vomiting episodes in the post-anesthesia care unit and at home will be measured. Up to 48 hours post-operatively
Secondary Quality of Recovery Score measured by the Quality of Recovery 15 Questionnaire The Quality of Recovery 15 (QoR-15) is a 15-item questionnaire that assesses patient-reported pain, physical comfort, physical independence, psychological support, and emotional state. Questions are rated in an 11-point scale (0-10), where a higher score indicates a better outcome. The QoR-15 takes an average of 2.5 minutes to complete. The QoR-15 has been statistically validated and is designed for both ambulatory and inpatient surgery populations. The QoR-15 will be completed at baseline prior to surgery and 24 hours after surgery. Baseline (prior to surgery) and 24 hours after surgery
Secondary Length of stay in hospital in hours Measured from the time admitted to PACU to the time discharged from hospital. LOS includes time in the PACU, Surgical Day Care (SDC) and, if required, Inpatient Unit. Patients are transferred between units and discharged from hospital according to standardized institutional criteria Up to 96 hours post-operatively
Secondary Time to perform ultrasound-guided TPVB+PecsII Measured in minutes. Up to 24 hours post-operatively
Secondary Time under general anesthesia Measured in minutes. Up to 24 hours post-operatively
Secondary Time in PACU Measured in minutes. Up to 24 hours post-operatively
Secondary Number of participants with failure of discharge from PACU and requiring admission to hospital Categorical. Up to 24 hours post-operatively
Secondary Number of participants requiring rescue opioid analgesics and anti-emetics. Rescue medication are defined as those required "as needed" (ie. Beyond scheduled) in the PACU, ward and after discharge. Up to 7 days post-operatively
Secondary Time to rescue opioid analgesics and anti-emetics. Rescue medication are defined as those required "as needed" (ie. Beyond scheduled) in the PACU, ward and after discharge. Time to rescue medications is measured in minutes. Up to 7 days post-operatively
Secondary Number of participants with failure of early discharge. Failure of early discharge is defined as emergency room visits within 48 hours of discharge Up to 48 hours post-operatively
Secondary Number of participants with complications and adverse events Related to the ultrasound-guided regional block: vascular or nerve injury, Horner's syndrome, bleeding/hematoma, local anesthetic systemic toxicity, pneumothorax, distortion tissue planes during axillary dissection, and other.
Related to the surgery: hematoma, tissue necrosis, urgent unplanned return to the operative theater within 24 hours of surgery.
Up to 24 hours post-operatively
See also
  Status Clinical Trial Phase
Completed NCT04633850 - Implementation of Adjuvants in Intercostal Nerve Blockades for Thoracoscopic Surgery in Pulmonary Cancer Patients
Completed NCT03652103 - Efficiency of Erector Spinae Plane Block For Patients Undergoing Percutaneous Nephrolithotomy Phase 4
Completed NCT03631914 - Intelligent Needle Tip Tracking Using Ultrasound Imaging for Infraclavicular Brachial Plexus Blocks N/A
Completed NCT03244631 - Pain Control in Hip Arthroscopy: Comparing Lumbar Plexus Versus Peri-capsular Injection N/A
Completed NCT05034601 - ESPB vs TPVB for Postoperative Analgesia After the Nuss Procedure N/A
Completed NCT03740815 - Feasibility of Serratus Plane Block Associated With Sedation in Axillary Dissection N/A
Not yet recruiting NCT03978780 - Erector Spinae Block vs. Placebo Block Study N/A
Not yet recruiting NCT04101019 - Sphenopalatine Ganglion Block to Treat Shoulder Pain After Laparoscopic Surgery N/A
Recruiting NCT02903719 - The Effect of Phrenic Nerve Block on Postoperative Shoulder Pain in Patients for Liver Resection. Phase 4
Completed NCT03211949 - Ultrasound Guided Topographic Mapping of Medial Antebrachial Cutaneous Nerve N/A
Completed NCT05549011 - PENG vs SIFI Block for Positioning Pain During Spinal Anesthesia
Suspended NCT03291691 - Protective Nerve Stimulation in Regional Anesthesia
Completed NCT03771742 - Modified Paramedic Sagittal vs. Transverse TMQLB N/A
Recruiting NCT04480320 - Sonography-guided Pericapsular Never Group Block for Hip Arthroplasty N/A
Active, not recruiting NCT05555147 - The Effect of Bilateral Infraorbital and Infratrochlear Nerve Block on Perioperative Period of Hypophysectomy N/A
Not yet recruiting NCT04298580 - Timing Effect of Ultrasound-Guided PVB After Robotic Cardiac Surgery N/A
Completed NCT03658421 - Dexmedetomidine as Adjuvant for FNB in TKA N/A
Completed NCT03667898 - Intelligent Needle Tip Tracking Using Ultrasound Imaging for Lumbar Plexus Blocks N/A
Terminated NCT03316118 - US Guided GNB vs Saline Injection for TKA Phase 4
Completed NCT03317600 - Postamputation Pain: Peripheral Mechanisms N/A