Hershey, PANCT03737292Now EnrollingIRB Ready

Pain, Postoperative Clinical Trial in Hershey, PA

Access cutting-edge pain, postoperative treatment through this clinical trial at a research site in Hershey. Study-provided care at no cost to qualified participants.

Sponsored by Milton S. Hershey Medical Center

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Expert Care in Hershey

Access pain, postoperative specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related pain, postoperative treatment provided free

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Check if you qualify for this pain, postoperative clinical trial in Hershey, PA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Hershey

    Convenient for PA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Hershey site if eligible
  4. 4Begin participation

About This Pain, Postoperative Study in Hershey

The purpose of this study is to assess pharmacokinetics of liposomal bupivacaine (Exparel) after multilevel intercostal injections of this local anesthetic for pain control during and after thoracoscopic surgeries. The specific aim of this study is to evaluate plasma concentration of bupivacaine after intraoperative intercostal injections of 266 mg of liposomal bupivacaine and compare it to plasma concentrations of bupivacaine after intercostal injections of 2mg/kg of 0.5% plain Bupivacaine with maximal dose of 30 ml or 150 mg. The hypothesis of the study is that plasma concentration of bupivacaine after intercostal injections of 266 mg of liposomal bupivacaine will be similar to concentrations after injections of plain bupivacaine, and will remain below the toxic level threshold range of 2000-3000 ng/mL (2-3 mg/L) at which central nervous system and cardiovascular adverse events would be expected to occur. The secondary objective is to evaluate if intercostal injections of 266 mg of liposomal bupivacaine will significantly reduce opioid consumption and postsurgical pain, within the first 48 hours and up to 3 months after minimally invasive thoracic surgeries, to determine if both acute and chronic post-thoracotomy pain can be decreased by intraoperative intercostal injections of liposomal bupivacaine. Additionally, the rate of pneumonia, the rate of atrial fibrillation and length of hospital stay will be assessed as secondary outcomes after thoracic surgeries. These outcomes can be affected by the level of postoperative pain and inflammation. Significance of this study: If positive, the results of this research have the potential to significantly improve pain management after thoracoscopic surgery. Based on prior experience, prolonged analgesia after liposomal bupivacaine injection is safe, and may help reduce perioperative opioid consumption and decrease opioid related complications. It will improve patient comfort, eliminate need for indwelling neuraxial catheters and risks associated with them.

Sponsor: Milton S. Hershey Medical Center

Who Can Participate

Inclusion Criteria

1\. Male or female patients over age 18 undergoing minimally invasive thoracic surgeries including but not limited to:
VATS wedge resection /segmentectomy
VATS lobectomy.
Robot assisted thoracoscopic wedge resection/segmentectomy.
Robot assisted thoracoscopic lobectomy procedures.

Exclusion Criteria

Patients under18 years of age
Patients weighing less than 48 kg
Pregnant and lactating females will be excluded from the trial
Patients preoperatively taking narcotics for chronic pain in proximity to surgical site
Patients with previous ipsilateral thoracic surgery
Patients undergoing pleurectomy/mechanical pleurodesis.
Patients with high likelihood of conversion from thoracoscopic procedure to open thoracotomy as determined by an operating surgeon
Patients with pre-existing painful conditions (CRIPS, fibromyalgia, neuropathy)
Patients unable to reliably communicate pain scores such as patients with dementia, alterations in mental status
Patients with hypersensitivity to local anesthetics and pain medications used in the study
Patients with previous thoracic spine surgeries
Patients with increased creatinine (over 1.5mg/dl)
Patients with liver dysfunction
Non-English speaking patients

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Hershey?

Yes, this clinical trial (NCT03737292) has an active research site in Hershey, PA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Pain, Postoperative Treatment Options in Hershey, PA

If you're searching for pain, postoperative treatment options in Hershey, PA, this clinical trial (NCT03737292) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Hershey research site is actively enrolling participants for this clinical trial. You'll receive care from experienced pain, postoperative specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all pain, postoperative clinical trials near you to find additional studies recruiting in your area.

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