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NCT04606264RECRUITINGIRB Ready

Recommendations of Enhanced Recovery Interventions for Patient's Clinical Team and Collection of Associated Data

Sponsored by Jennifer Holder-Murray

Quick Self-Assessment

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1 of 2500 participants interested
0% interest

Express Your Interest Today

Interested in learning more? Complete the form below.

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Advance Medical Science

    Contribute to groundbreaking research

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel (varies by study)

  • Help Others

    Benefit future patients

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3In-person assessment if eligible
  4. 4Begin participation

About This Study

This REMAP Periop ERP domain study falls under the Periop Core Protocol, which compares the different recommended strategies for enhancing recovery through the use of various standard of care treatments before, during and after surgery in all patients with elective surgical encounters at UPMC who meet eligibility criteria.

Who Can Participate

Inclusion Criteria

Patient is seen in preoperative appointment prior to surgery 2. ≥ 18 years of age 3. Anticipated overnight hospital stay 4. Scheduled for elective abdominal surgery that utilizes ERP PowerPlans - placed into the patient's electronic chart at least one night before surgery 5. ERP Abdominal Complex Pathway PowerPlan (used for colorectal and gastrointestinal surgery) 6. ERP Bariatric Surgery Pathway PowerPlan 7. ERP Gynecology Oncology Pathway PowerPlan 8. ERP Whipple/Pancreas Pathway PowerPlan 9. ERP Open Liver Resection Pathway PowerPlan 10. Surgery is scheduled for one of the following UPMC sites: 11. UPMC Presbyterian Hospital 12. UPMC Passavant Hospital 13. UPMC Magee-Women's Hospital

Exclusion Criteria

Critera 1. Death is deemed to be imminent or inevitable 2. Patient is pregnant \< 18 years of age 3. Patients undergoing emergent/urgent surgery 4. Patients that are pregnant 5. Patients that have an eligible PowerPlan ordered less than one night before surgery

❓ Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility during the screening process.

Study Details

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Study Type

INTERVENTIONAL

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Target Enrollment

2500 participants

Gender

ALL

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Sponsor

Jennifer Holder-Murray

Study Locations

Choose your preferred location or select flexible during enrollment

Unknown

Pittsburgh

Pennsylvania

Location available
Unknown

Pittsburgh

Pennsylvania

Location available
Unknown

Pittsburgh

Pennsylvania

Location available

Frequently Asked Questions

Q:What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Q:Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Q:Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

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

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

Q:How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

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

Ready to Make a Difference?

Express your interest in this groundbreaking clinical trial

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Looking for Abdominal Surgery Treatment in Pittsburgh?

Join others in Pennsylvania exploring innovative treatment options through clinical research

Abdominal Surgery Treatment Options in Pittsburgh, Pennsylvania

If you're searching for Abdominal Surgery treatment in Pittsburgh, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Pittsburgh, Pittsburgh, Pittsburgh and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Abdominal Surgery. All study-related care is provided at no cost to participants.

Local Sites
3 locations in Pennsylvania
Now Enrolling
Up to 2500 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Abdominal Surgery?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Abdominal Surgery

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Abdominal Surgery Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT04606264. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.