Transitional Pain Service for Postoperative Pain

(TPS-Select Trial)

MH
AS
Overseen ByAkash Shanmugam, BS
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: University of California, San Francisco
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to determine if the Transitional Pain Service program can help surgical patients manage pain more effectively and reduce opioid use after surgery. Researchers seek to discover if this approach can prevent long-term pain and if a computer tool can better identify patients at risk. Participants will receive either their usual care or additional support, such as pain education and mental health resources, before and after surgery. This trial suits patients planning surgery at UCSF who are at higher risk for chronic pain afterward, as identified by a computer model. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to potentially groundbreaking pain management solutions.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that the Transitional Pain Service is safe for managing postoperative pain?

Research has shown that treatments in the Transitional Pain Service (TPS) are safe for patients. In previous studies, patients using TPS experienced less pain and required fewer strong painkillers 90 days after surgery. This indicates that the service effectively manages pain and is well-tolerated by patients.

In addition to TPS, psychological support and pain education are included in the treatment. Studies have found that educating patients about pain before surgery aids in recovery and pain management. This education is safe and carries no significant risks.

Overall, both TPS and psychological support have demonstrated positive results and are considered safe for surgical patients. Participants can rely on the safety of these treatments based on existing research.12345

Why are researchers excited about this trial?

Researchers are excited about the Transitional Pain Service because it offers a comprehensive approach to managing postoperative pain, unlike the typical focus on medication alone. This service includes psychological management, pain education, and personalized support like mental health screenings and referrals, which are not standard in usual care. Additionally, it empowers patients to be actively involved in their recovery process by choosing the level of participation that suits them, potentially leading to better outcomes and patient satisfaction.

What evidence suggests that the Transitional Pain Service is effective for managing postoperative pain?

Studies have shown that the Transitional Pain Service (TPS), which participants in this trial may receive, can reduce the need for opioids after surgery and improve pain management. Specifically, nerve blocks in TPS significantly ease post-surgery pain and decrease opioid use. Research also indicates that pre-surgery education on pain management leads to less pain afterward. Patients who receive this education often report better pain control and use fewer opioids. Overall, TPS combines these methods to support better recovery and pain control after surgery.12678

Who Is on the Research Team?

AB

Andrew Bishara, MD

Principal Investigator

UCSF Department of Anesthesia

Are You a Good Fit for This Trial?

This trial is for adult surgical patients at risk of developing long-term pain after surgery. It aims to see if a Transitional Pain Service (TPS) can prevent chronic pain and reduce opioid use post-surgery. Participants will be compared with those receiving usual care.

Inclusion Criteria

I am 18 years old or older.
I am scheduled for elective surgery at UCSF.
Patients must be identified as higher risk for chronic pain after surgery by a computer model
See 1 more

Exclusion Criteria

I am experiencing severe depression with thoughts of suicide.
Patients with serious memory or thinking problems that make participation difficult
I have surgery planned within the next month.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pre-Surgery Support

Participants receive educational videos, meetings with a pain pharmacist, mental health screening, and physical therapy to prepare for surgery

2-4 weeks

Post-Surgery Support

Participants receive coordinated support including pain-relief procedures, medication management, and outpatient therapies to optimize recovery

12 weeks
Regular follow-ups as needed

Follow-up

Participants are monitored for pain levels, opioid use, and healthcare costs at 30, 60, and 90 days after discharge

12 weeks
3 visits (virtual or in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Interventional Pain Procedures
  • Psychological Management and Pain Education

Trial Overview

The study tests the effectiveness of TPS in managing postoperative pain versus usual care, using an AI algorithm to identify patients at high risk for persistent pain. The program includes pharmacologic management, psychological support, education, physical therapy, and interventional procedures.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Transitional Pain ServiceExperimental Treatment5 Interventions
Group II: Usual CareActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, San Francisco

Lead Sponsor

Trials
2,636
Recruited
19,080,000+

Citations

Nerve Blocks for Post-Surgical Pain Management: A Narrative ...

Nerve blocks show great promise as effective alternatives for managing post-surgical pain. They can reduce the need for opioids and their side effects.

Transitional Pain Service: An Update - PMC - PubMed Central

In most of these studies, the main outcome measured was the reduction in postoperative opioid use in surgical patients. In one of the first such ...

Clinical practice guidelines for postoperative pain ...

Effectiveness of peripheral nerve blocks for postoperative pain management, Recommendation 11: Peripheral nerve blocks are recommended as an essential ...

Study Details | NCT07296770 | An Artificial Intelligence ...

The goal of this clinical trial is to learn whether a pain-management program called a Transitional Pain Service can help prevent long-term ...

Full article: Interventional Pain Procedures: A Narrative ...

One RCT of ITDD demonstrated reduced pain, improved clinical success in pain control, significantly relieved common drug toxicities, and greater survival in ...

Ten years of transitional pain service research and practice

Analysis of the primary outcome showed that 90 days after surgery, TPS patients (13.4%) were significantly less likely to be taking opioids than the non-TPS ...

Transitional Pain Services: Closing the Gap Between Acute ...

Data from transitional pain services highlight that patients who are engaged in early intervention with acceptance and commitment training ...

Interventional Pain Procedures: A Narrative Review ...

Overall, the goal of interventional pain procedures is to improve the patient's quality of life and to provide effective pain management.