Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT05992896 |
| Other study ID # |
23-003451 |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
Phase 4
|
| First received |
|
| Last updated |
|
| Start date |
September 26, 2023 |
| Est. completion date |
December 2024 |
Study information
| Verified date |
May 2024 |
| Source |
Mayo Clinic |
| Contact |
Joshua Druckrey |
| Phone |
715-838-5831 |
| Email |
druckrey.joshua[@]mayo.edu |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The purpose of this research is to find out if using liposomal bupivacaine solution
(bupivacaine liposome) injections during lower extremity revascularization surgery will lower
the amount of narcotic drugs used during and following the procedure.
Description:
This will be a single site, triple blinded, controlled randomized trial assessing potential
reduction in narcotic use in patients undergoing lower extremity revascularization, when
loco-regional anesthesia with Exparel solution is performed, compared to normal saline
injection. Loco-regional anesthesia for lower extremity revascularization will include an
ultrasound guided ilio-inguinal block with Exparel solution and local injection in the
wound(s) edges of more Exparel solution. The control group will receive injection of normal
saline instead. Lower extremity revascularizations will include femoral endarterectomy with
patching ± antegrade or retrograde endovascular intervention (one or more combination of
stenting, atherectomy, balloon angioplasty) or bypass (femoral popliteal or femoral tibial
bypasses with vein or prosthetic graft).
The study will be conducted at Mayo Clinic Health System in Eau Claire only (single site).
The enrolled patients will be medicated in pre- and intra-operative phases by the anesthesia
team in a standardized fashion, based on the protocol in attachment 4.
Patient, surgeon, and the team assessing the patient postoperatively will be blinded (triple
blinded). Normal saline will be opacified by the pharmacy to keep the surgeon unaware of what
he/she is injecting. As per Mayo policy, all patients will receive the surgical bill at least
30 days after surgery. This time frame will allow the patient to remain blinded if he/she
received Exparel injection for the entire length of the study (which is 28 days after
surgery).
The rounding team will evaluate the patient for signs of complications (based on the
Clavien-Dindo grading system; figure 1) and ask the patients their minimum and maximum pain
score (reported as 0-10 verbal numerical rating scale with 10 being worst pain) in the first
72 hours. The nurse will also assess patient's pain with the Visual Analogue Score (VAS;
Figure 1). If VAS is >3 after the non-narcotic medications have been given, oral or
intravenous narcotic medication will be administered. If patient is discharged before 72
hours, the team will call the patient at 48 and 72 hours to assess pain score. The maximal
pain score value for the time period 0-72 hours will be chosen as the maximal pain during
that time period.
Discharge criteria include pain <4/10, independence of intravenous analgesia, and being
medically stable for discharge. If patients are waiting for placement, the time of discharge
for the purpose of the study will be the day they have met such criterion as opposed to the
day of actual discharge, as this can vary depending on patient placement.
The nurses taking care of the study patients will fill a specific form (attachment 1) every
time a narcotic medication will be administered, specifying the pain score at the time of the
administration and the location of the pain. The filled form will be handled to the rounding
team on a daily basis.
The amount of postoperative narcotic use will be calculated in morphine equivalent. Inpatient
narcotic use will be extrapolated from the patient's chart and the nursing forms. Outpatient
narcotic use will be based on the narcotic prescription(s) filled by the patient. A urine
drug screen will be obtained at 14 days (at the time of the first postoperative clinic visit)
and at 28 days, but only in those patients who did not fill the narcotic prescription, to
make sure those patients did not obtain narcotics from other sources.
Patient quality of recovery and satisfaction will be assessed with a patient survey
administered the day of discharge and at 30 days (see attachment 2). For quality of recovery
measurement, we used the validated and psychometrically evaluated questionnaire QoR-15 from
Stark and colleagues, a short form of the comprehensive 40-item questionnaire QoR-40. (6,7).
At the time of the signature of the consent, the patients will receive educational materials
regarding use of narcotics and associated side effects (from the Center of Disease and
Prevention Control, Opioid Factsheet for Patients [cdc.gov]), covering the main points showed
in the attachment 3.(8) The educational material on narcotic use will be re-discussed with
the patients at the time of the discharge.
The research coordinator team will be in charge of randomizing patients and communicating the
result to pharmacy. Based on the results, pharmacy will send the solution (either Exparel or
"modified" normal saline to resemble Exparel) to inject during the ultrasound guided
ilio-inguinal block. As mentioned above, patient, surgeon, and rounding team will be blinded
(triple blind, randomized study). Demographics, pre-operative cardiovascular risk factors,
procedural details, intra- and post-operative complications, hospital stay, patient recovery
satisfaction, intraoperative narcotic use (in morphine equivalent), postoperative narcotic
use (in morphine equivalent) at 12, 24, 48, and 72hr, total postoperative narcotic use (in
morphine equivalent) at 28 days ilio-inguinal block will be recorded in a redcap database.
Treatment technique:
The patient will be brought to the operative room and general anesthesia initiated in supine
position. After the patient will be prepped and draped in standard sterile fashion, the new
intervention, for which this study is designed, will include identifying the transversus
abdominis muscle with ultrasound guidance, few centimeters above the anterior superior iliac
spine, in the surgical side. Using sterile technique, an 20g Nerve block needle will be
inserted and advanced under ultrasound guidance until it is below the fascial covering of the
transversus abdominis muscle layer. Gentle aspiration for air, or blood will be performed and
either 30 cc mix of 1 vial of Liposomal bupivacaine/1 vial of 0.25% bupivacaine/100 cc of
saline or 30 mL of normal saline will be injected under ultrasound guidance. For each 5cc of
local anesthetic injected, aspiration will be performed. Upon completion of the injection,
the needle will then be removed. In the control group, the same technique will be utilized
but normal saline alone will be injected instead. The solution of normal saline with be
opacified by pharmacy to resemble Exparel solution and to keep the surgeon blinded. Both the
patient and the surgeon will be not aware of the solution injected.
During the procedure, after the plan of dissection is completed and the target vessels
exposed and controlled, the edges of the wound(s) will be injected with the remaining mix of
Liposomal bupivacaine/bupivacaine/saline (or normal saline alone in the control group). The
revascularization will continue as per standard of care. At the end of the revascularization,
the wound(s) will be closed in multiple layers. Once the procedure is completed, the patient
will be sent to the recovery room and eventually to the hospital room.
Recruitment:
Consenting Procedure:
Before any procedure is performed, informed consent will be obtained. A single informed
consent form that describes both the study procedures will be discussed with the patient
including pros and cons of injection of Exparel or normal saline, side effects and potential
complications of these medications.
Patients need to agree to perform a urine drug test at 14 and 28 days if required (see
below), filled the survey questionnaire for patient's recovery satisfaction, provide the
highest pain score.
The attending provider or the team nurse practitioner, resident or research coordinator will
obtain the consent. These individuals would have basic medical education and degree necessary
for proper explanation of the details of the study and the medical implications involved.
Patients will be reconsented if needed after any major change in clinical condition or
adverse events reporting. A copy of the signed informed consent will be kept in the medical
record and a digital copy maintained on a password protected secure file.
Patients will be randomized following consent and subsequently evaluated with intention to
treat. Randomization will be performed by the research coordinator. During the inpatient
hospital phase of their recovery patients will be assessed by the rounding team for pain
score and postoperative complications. Following discharge patients will be seen in clinic at
14 days for wound check, pain control, patient's recovery satisfaction and narcotic use. If
no narcotic prescription has been filled until then, a urine drug test will be administered
to make sure the patient did not take narcotic medication from other sources. At 28 days, a
clinic follow up will be performed to check wound(s), pain control, recovery satisfaction and
narcotic use. If no narcotic prescription has been filled, a urine drug test will be
administered to make sure the patient did not take narcotic medication from other sources.
Enrollment, Baseline, and/or Randomization Enrollment Enrollment can occur at any time
between preoperative clinic visit and the day of surgery. A patient is enrolled once passed
inclusion criteria, study procedure explained to them by a qualified practitioner and have
signed informed consent. Enrollment date is the day of signing the consent form. That would
be the same day randomization will be done.
Once patients are enrolled and consented, they will be registered in the trial.
Prior to accepting the registration/randomization, the registration/randomization application
will verify the following:
- IRB approval at the registering institution
- Patient eligibility
- Existence of a signed consent form
- Existence of a signed authorization for use and disclosure of protected health
information
A patient is deemed ineligible if after registration, it is determined that at the time of
registration, the patient did not satisfy each and every eligibility criteria for study
entry. The patient may continue treatment off-protocol at the discretion of the physician as
long as there are no safety concerns, and the patient was properly registered. The patient
will go off study.
If the patient received treatment, all data up until the point of confirmation of
ineligibility must be submitted. If the patient never received treatment, on-study material
must be submitted.
A patient is deemed a major violation, if protocol requirements regarding treatment are
severely violated that evaluability for primary end point is questionable. All data up until
the point of confirmation of a major violation must be submitted. The patient will go off
study. The patient may continue treatment off-protocol at the discretion of the physician as
long as there are no safety concerns, and the patient was properly registered.
A patient is deemed a cancel if he/she is removed from the study for any reason before any
study treatment is given. On-study material and the End of Active Treatment/Cancel
Notification Form must be submitted. No further data submission is necessary.
Baseline Assessments Baseline assessment will include review of medical history, physical
examination by treatment team, review of medications, and labs by the individual obtaining
consent.
Randomization Randomization will be done once patients are enrolled. Upon patient discharge
from the hospital, initiation of study intervention will occur. After the patient has been
registered into the study, Randomization will be performed by an inpatient pharmacist at Mayo
Clinic Eau Claire using an online randomizer, the patient will be assigned to one of the
following treatment groups- Exparel or control with normal saline.
Follow-up Visits Patients will be seen for an in-person follow-up visit between POD 14 and
28. Treatment administration form, vitals, and adverse events will be reviewed at follow-up
appointment. For patients who did not fill the narcotic prescription, a urine drug test will
be administered at 14 and/or 28 days to make sure those patients did not take narcotic
medication from other sources.
