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Completed

NCT Number: NCT02052557

The Effect of Exparel on Post Operative Pain and Narcotic Use After Colon Surgery

The purpose of the study is to evaluate the effect of Exparel on pain control and patient outcome after colon resection. The investigators will evaluate the clinical course of the patients who receive exparel as compared to the patients who do not receive exparel. Exparel is a 72 hour bupivacaine which is slowly released from lysosomes over the course of three days. A long acting local anesthetic should provide better pain control than conventional bupivacaine which has a 3.5 hour half-life.

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Key information

About this study

Patients who are undergoing elective colon resection with Dr. Kraemer and Dr. Raman will be offered participation in the study. This will include robotic, laparoscopic and open procedures.

In the pre-operative area prior to surgery, the surgical resident will inform the patient of the opportunity to participate in the research study. The resident will consent the patient at that time, if the patient chooses to participate, they will be randomized to an exparel or non-exparel group. The randomization will be done by having the resident pick an envelope that will state whether or not the patient is randomized to the exparel or non-exparel group, this will randomize to 50% in each group. The patient will not be notified of the type of local anesthetic they receive. The attending surgeon will also be blind to the type of local the pt will receive; only the resident and Operating Room (OR) staff will know what type of local anesthetic was given. Unfortunately the opaque color of the exparel precludes the physician injecting the local anesthetic from being blinded to the type of anesthetic given.

The patient will be taken to the operating room as usual, and the surgery will proceed as it normally would. At the end of the surgery the patient will receive either exparel or bupivacaine depending upon which the patient was randomized to. The attending surgeon will not be in the operating suite while the local anesthetic is being injected. 30 milliliters (mL) of either exparel or bupivacaine will be injected into the subcutaneous tissues at the end of surgery.

The patient will be taken to the post operative care unit (PACU), the medications for post-operative pain will be standardized between the two groups, a standard starting dose on the patient controlled analgesia (PCA) will be used, and will be adjusted as needed. The postoperative care will attempt to be standardized in regard to diet, discharge (dc) of foley, not using nasogastric (NG) tubes, however this will be based on the individual patient was what is best for their care. This data will then be analyzed to determine if exparel has a beneficial effect on surgical care.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elective colon resection for both benign and malignant disease
  • Laparoscopic, robotic and open techniques

Exclusion criteria

  • emergent colon cases
  • cases preformed by surgeons other than Dr. Raman or Dr. Kraemer
  • pregnant patients
  • patients currently breast feeding
  • patients under the age of 18
  • other patients unable to give informed consent
  • bupivacaine use within 96 hours
  • allergy to amide anesthetics
  • prisoners
  • caution will be used in patients with renal or hepatic failure.

Treatment and study plan

Bupivacaine

Drug

30ml of bupivacaine were injecting into the subcutaneous tissue at the incision sites after surgery in the OR

Other names: Marcaine

Bupivacaine liposome suspension

Drug

30ml of Bupivacaine liposome injectable suspension were injecting into the subcutaneous tissue at the incision sites after surgery in the OR

Other names: Exparel, 72 hour Bupivacaine, Long acting Bupivacaine

Primary outcomes

  1. PCA (Patient Controlled Analgesia) Usage

    Time frame: 48 hours post operatively

    Will measure the amount of PCA use for the first 48 hours after surgery.

Secondary outcomes

  1. Oral Pain Medications

    Time frame: 48 hours postoperatively

    the amount of post operative oral narcotic is measured post op

  2. Total IV (Intravenous) Narcotic Used

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days

    the total amount of IV narcotic is measured that is given during post op period prior to discharge

  3. Total Oral Narcotic Used

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days

  4. Length of Stay

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days

  5. Return of Bowel Function

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days, and the timing of return of bowel function returning will be recorded

  6. Readmission

    Time frame: 30 days post operative readmission

  7. Toradol Use

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days

  8. Ofirmev

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days, and the amount of ofirmev used during admission will be recorded

  9. Nausea Medication

    Time frame: The amount of nausea medicine used 48 hours post op was recorded

  10. Foley Catheter Removal

    Time frame: participants will be followed for the duration of hospital stay, an expected average of 3 days, the timing of foley catheter removal will be recorded

  11. Postoperative Pain

    Time frame: POD #3-5 and POD #13-15

    The investigators will talk to the patient after surgery immediately post operatively Post Operative Day (POD) #3-5 and POD #13-15 and ask the patients to rate their pain on a scale of 1-10.

  12. Post Operative Satisfaction

    Time frame: POD #3-5 and POD #13-15

    The investigators will ask the patient to rate their satisfaction with pain control.

  13. Home Oral Narcotic Use

    Time frame: POD #13-15

    The investigators will ask the patients how many of their narcotic pain pills they used after surgery up to the POD #13-15

Other outcomes

  1. NG (Nasogastric) Placement

    Time frame: POD #0 if NG was placed

    We recorded if an NG was placed immediately post operatively

Sponsors and collaborators

Lead sponsor

Des Moines University

Other

Collaborators

  • Mercy Medical Center

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Feb 3, 2014
Registry last updated
Jan 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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